Veru Inc (VERU) 2021 Q2 法說會逐字稿

Good morning, ladies and gentlemen, and welcome to the Veru Inc.'s Investor Relations Conference Call. (Operator Instructions) Please note that this event is being recorded. I would now turn the conference over to Mr. Sam Fisch, Veru Inc.'s, Director of Investor Relations. Please go ahead.

Good morning. The statements made in this conference call may be forward-looking statements. Forward-looking statements may include, but are not necessarily limited to, statements of the company's plans, objectives, expectations or intentions, regarding its business, operations, finances and development and product portfolio. Such forward-looking statements are subject to known and unknown risks and uncertainties, and our actual results may differ significantly from those projected, suggested or included in any forward-looking statements. Risks that may cause actual results or developments to differ materially are contained in our 10-Q and 10-K SEC filings. I would now like to turn the conference call over to Dr. Mitchell Steiner, Veru Inc.'s Chairman, CEO and President.

Thank you, Sam, and good morning. With me on this morning's call are Michele Greco, CFO and CAO; Michael Purvis, EVP, General Counsel and Corporate Strategy and Sam Fisch, Director of Investor Relations. Thank you for joining our call. Veru is a late clinical-stage oncology biopharmaceutical company focused on developing novel medicines for the management of 2 of the most prevalent cancers: prostate cancer and breast cancer. We continue to invest cash generated from our sexual health commercial business into the clinical development of our potentially high-value oncology drug candidate, so that our shareholders might realize the maximum value of our oncology biopharmaceutical company. This morning, we will discuss the progress of our late clinical stage prostate cancer and breast cancer drug pipelines, as well as the sabizabulin, the new name for VERU-111, Phase 3 study for the treatment of COVID-19. We'll then provide financial highlights for our second quarter of fiscal year 2021.

In oncology, we're focused on providing new and novel oral therapies with unique mechanisms of action and favorable safety profiles for both advanced prostate and breast cancers. Veru anticipates registration clinical trials for up to 4 oncology indications and the additional registration Phase 3 clinical trial for sabizabulin for COVID-19, makes a total of 5 potentially registration enabling clinical trials to commence in calendar year 2021.

Prostate cancer. The Company continues to make strong clinical progress advancing sabizabulin as a treatment for metastatic castration and androgen receptor targeting agent with resistant prostate cancer and VERU-100 for androgen deprivation therapy for metastatic prostate cancer. Sabizabulin, which as I mentioned is the new name for VERU-111 is an oral first-in-class new chemical entity that targets crosslinks and the swaps alpha and beta tubulin subunits of microtubules to disrupt the cytoskeleton. And in prostate cancer, this also results in the disruption of the androgen receptor transport from the of cytoplasm into the nucleus. Sabizabulin is being evaluated in open label Phase 1b study in men with metastatic castration and androgen receptor targeting agent-resistant prostate cancer.

The Phase 1b/2 clinical study enrolled 39 men in the Phase 1 and 41 men in the Phase 2 portion. The Phase 2 portion is completely enrolled and still ongoing. The safety of sabizabulin appears to be similar to an AR targeting agent like abiraterone, enzalutamide based on what has been reported in literature. Long term daily chronic administration of the drug appears to be feasible and safe. We have patients in the Phase 1b portion that have reached 2 years of treatment without evidence of prostate cancer tumor progression. At the recommended Phase 2, 63-milligram oral daily dose, the most common adverse events were mostly Grade 1 and 2 diarrhea, fatigue and nausea. There have been no reports of neutropenia, significant neurotoxicity or hair loss.

The Phase 1b/2 study has -- also has yielded promising and significant efficacy outcomes. The efficacy results show PSA declines and responses as well as objective and durable tumor responses, including partial and complete responses. Furthermore, the median radiographic progression-free survival in men who had at least one 63-milligram dose of sabizabulin was 12 months. As there are approximately 10 men still on study, the median progression-free survival in the Phase 2 portion has not been reached.

We also conducted a PK study to compare the Phase 1b/2 dosage formulation with the Phase 3 dosage formulation. Measured blood concentrations of sabizabulin at the 63-milligram Phase 1b/2 dose or similar to the 32-milligram Phase 3 dose, which means the Phase 3 dosage formulation has better oral bioavailability. The scientific abstract reporting the Phase 1b/2 safety and efficacy results has been accepted for presentation at the upcoming ASCO scientific meeting, which will be held June 4 through the 8 -- into -- June 4 to the 8, 2021 and it's entitled sabizabulin VERU-111, an oral cytoskeleton disruptor to treat men with metastatic castration-resistant prostate cancer who have failed an androgen receptor targeted agent to be presented by Marc -- Dr. Mark Markowski, Assistant Professor of Oncology at the Sidney Kimmel Comprehensive Cancer Center and Johns Hopkins University School of Medicine and principal investigator on the study.

The company has also reached agreement with the FDA on the Phase 3 clinical trial design for sabizabulin, and we plan to enroll the first patient in the Phase 3 registration study by the end of this month. The Phase 3 VERACITY study is an open-label randomized study evaluating the efficacy and safety of sabizabulin 32-milligrams oral daily dosing versus an alternative androgen receptor targeted agent in men with metastatic castration-resistant prostate cancer who have failed at least one androgen receptor targeting agent with prior to IV chemotherapy. The primary endpoint is median radiographic free survival.

This study will be a 2:1 randomization, the trial assumptions expect a median radiographic progression-free survival of 7.4 months for sabizabulin versus 3.7 months for the alternative androgen receptor targeted agent, which if achieved would represent a doubling in the improvement in median radiographic progression-free survival, with sabizabulin compared to the active control. Statistically, using an alpha of 0.05 a power of 98% and a dropout rate of 30%, the study size will be approximately 245 subjects. We expect enrollment to take 10 months recruitment time and 12 months follow-up after the last patient is first dosed. The study will be conducted in 45 clinical sites across the United States, and the lead principal investigator will be Dr. Robert Dreicer, Deputy Director, University of Virginia Cancer Center, Director of Solid Tumor Oncology and Professor of Hematology and Oncology.

Sabizabulin if approved, will address a large part of the metastatic prostate cancer market, the use of an androgen receptor targeted agents like enzalutamide and apalutamide have moved earlier in the treatment sequence of advanced prostate cancer. The two currently approved indications for androgen receptor targeting agents and for hormone-sensitive metastatic prostate cancer and for non-metastatic castration-resistant prostate cancer. When patients progress or fail an androgen receptor targeted agent in both of these settings, they now have metastatic castrate-resistant and androgen receptor targeted agent-resistant prostate cancer, the very indication we're pursuing in the Phase 3 clinical trial. That -- this means that as meant as 90% of all advanced prostate cancer patients whose only other option would be to proceed to IV chemotherapy, could potentially benefit from this -- from sabizabulin. But being an orally administered drug with a side effect profile that appears to be similar to an alternative AR targeting agent, sabizabulin could be potentially prescribed by the urologist. This is important as urologists initially play an important role in the management of advanced prostate cancer patients. Typically, the urologist involves the medical oncologist when the patients require IV chemotherapy.

Next, I will update you on VERU-100 an androgen deprivation therapy for the treatment of hormone-sensitive metastatic prostate cancer. Androgen deprivation therapy, also known as ADT is currently the mainstay of advanced prostate cancer treatment, and is used as a foundation of treatment throughout the course of the disease. Furthermore, ADT is continued even as other endocrine chemotherapy radiation treatments are added or stopped. Standard medical practice for urologist and medical oncologists is to administer androgen deprivation therapy every 3 to 4 months in their office. These injections coincide with the follow-up office visits for metastatic or advanced prostate cancer. Furthermore, these injections are administered as a buy and bill product, and are reimbursed under Medicare Part B not Part D as in dog. So the urologist is compensated both with the drug and administering the drug. Therefore, urologists prefer injections over oral agents.

Gonadotrophin-Releasing hormone GnRH antagonist treatments are preferred, because castration occurs rapidly within a week, with no surges or flares in testosterone. Testosterone levels also tend to be lower, which is better for tumor control. GnRH antagonist also lower FSH levels, which is thought to be the reason why there are fewer cardiovascular side effects with GnRH antagonist versus GnRh agonist. There are no GnRH antagonist depot injection formulations commercially approved for treatment beyond one month duration. Veru-100 is a novel proprietary long-acting peptide, 3-month subcutaneous depot formulation injection designed to address the current limitations of commercially available in Androgen Deprivation -- commercially available Androgen Deprivation Therapy.

Happy to report that the GMP manufacturing scale-up is complete and we plan to start the open-label Phase 2 study in approximately 35 men to evaluate VERU-100 dosing by the end of this month. The open-label Phase 3 registration study, whose design has already been agreed upon by -- with FDA, will evaluate the efficacy and safety of VERU-100, approximately 100 men with hormone-sensitive metastatic prostate cancer, and is anticipated to start towards the end of the calendar year of 2021.

Next, I will discuss the progress of our breast cancer drug pipeline, which includes enobosarm and sabizabulin. The most common type of breast cancer which occurs in about 85% of women is ER-positive breast cancer, where estrogen is one of the main drivers of proliferation, tumor progression and metastasis. Consequently, treatments that target and block the estrogen receptor, so ER, are the mainstay of breast cancer therapy. According to the 2020 National Comprehensive Cancer Network guidelines, also known as the NCCN guidelines, the recommended first-line treatment in the metastatic setting is either a Non-Steroidal Aromatase Inhibitors in combination with a CDK4/6 inhibitor or fulvestrant in combination with a CDK4/6 inhibitor.

The recommended second-line treatment in the metastatic setting is fulvestrant in combination of the CDK4/6 inhibitor is a CDK4/6 inhibitor was not used in first-line metastatic setting. Unfortunately, almost all of the women being treated with these regimens will eventually develop resistance to the estrogen receptor blocking agent and a CDK4/6 inhibitor therapies, and there are limited clinical data that allow a recommendation for treatment continuing another CDK4/6 inhibitor for these patients in a third-line metastatic setting. Alternative treatment approaches that target novel pathways will be required, as there are limited treatment options following a CDK4/6 inhibitor and an estrogen receptor blocking agent resistance in the management of ER+HER2- metastatic breast cancer.

Interestingly, like the estrogen receptor, the androgen receptor is found in over 85% of breast cancer. What is the androgen receptors function in breast cancer and breast tissue? Does it stimulate or inhibit breast cancer growth? A recent publication in Nature Medicine of an international study headed by Dr. Hickey and her team, has provided scientific evidence establishing that the androgen receptor is a tumor suppressor in estrogen receptor positive breast cancer. This means, when the androgen receptor is activated by androgen, it strongly suppresses estrogen receptor breast cancer growth. This explains why historically, when synthetic androgens were used to treat breast cancer, they demonstrated good efficacy, but unfortunately the masculinizing side effects, increases in hematocrit and liver toxicity have prohibited their use as a viable treatment.

In contrast, enobosarm, an oral first-in-class new chemical entity is a selective androgen receptor targeted activating agent, and is being developed for the treatment of AR+ER+HER2-, metastatic breast cancer, and would represent the first new endocrine therapy for advanced breast cancer in decades. enobosarm has extensive non-clinical and clinical experience having been evaluated in over 25 separate clinical studies, involving more than 2,100 subjects, including 5 prior Phase 2 clinical studies in advanced breast cancer involving more than 250 patients.

In addition to suppressing androgen receptor positive, ER+ breast cancer cell proliferation and tumor growth, enobosarm has other potential beneficial clinical properties. In preclinical studies, enobosarm has demonstrated that it builds and heals cortical and trabecular bone, and therefore has the potential to treat osteoporosis and skeletal-related events. Enobosarm has also been shown to build muscle and to improve physical function, in clinical studies involving elderly subjects and patients with cancer cachexia including breast cancer patients. Furthermore, because of its tissue selectivity, enobosarm has a favorable side effect profile, with no masculinization, that's facial hair or acne, no increase in hematocrit and now liver toxicity.

The science supporting the efficacy of enobosarm by targeting the androgen receptor in ER+ advanced breast cancer was also the subject of the Nature Medicine studies published in February 2021, by an independent group of breast cancer experts led by Dr. Hickey. In their study, they showed that by using breast cancer tissue from patients who have resistance to estrogen receptor blocking agents and CDK4/6 inhibitor therapies, enobosarm monotherapy exhibited significant anti-tumor activity, while the combination of enobosarm plus a CDK4/6 inhibitor demonstrating even greater anti-tumor activity. They concluded that these data suggests the enobosarm restores the sensitivity of a CDK4/6 inhibitor-resistant breast cancer tissue to suppression by the CDK4/6 inhibitor.

2 positive Phase 2 studies involving 150 women with AR+ER+ metastatic breast cancer were conducted. We will focus on the second of these two studies, the G200802 Phase 2 study, which is a 2-arm study evaluating 9-milligram and 18-milligram of enobosarm daily dosing in 136 women with AR+ER+HER2- advanced breast cancer. The patients in this study were heavily pretreated, having failed an average of three estrogen receptor blocking agents, and 88% had received prior chemotherapy. Clinically meaningful tumor responses observed with enobosarm monotherapy, strongly establish the relevance of targeting the androgen receptor with the select androgen receptor activating agent in women, with heavily pretreated estrogen receptor blocking agent resistant AR+ER+, metastatic breast cancer. The 9-milligram dose was selected for our Phase 3 study as the 9-milligram cohort had similar tumor responses with a slightly better toxicity profile than the 18-milligram dose cohort. Focusing on the 9-milligram cohort, enobosarm monotherapy in the 802 Phase 2 study, had a favorable clinical benefit rate of 32% and an objective tumor response rate of 29.4%. enobosarm appeared safe and well tolerated without virilizing effects, increase in hematocrit or liver toxicity. Quality of life measurements demonstrated overall improvement, including mobility, anxiety, depression and pain.

We've also performed a post-hoc subset analysis of the Phase 2 clinical data, to understand whether enobosarm had any anti-tumor activity or efficacy in patients with AR+ER+ metastatic breast cancer, who were resistant to both an estrogen receptor blocking agents and CDK4/6 inhibitor. These data were presented at the European Society for Medical Oncology, ESMO, Breast Cancer Virtual Congress in 2021 that was held this past May -- actually earlier this month. In the subset analysis, enobosarm treatment in patients with measurable metastatic AR+ER+ breast cancer, who have progressed following treatment with an estrogen receptor blocking agent and a CDK4/6 inhibitor, in this case palbociclib, resulted in a clinical benefit rate at 24 weeks of 50%, and the best objective tumor response of 30% including 2 complete responses and one partial response. The overall mean radiographic progression-free survival for the 9-milligram group was 10 months.

Though small subset, one include that enobosarm has anti-tumor activity in women, with AR+ER+ metastatic breast cancer that is resistant to estrogen receptor blocking agents and CDK4/6 inhibitors. Furthermore, the presence and the degree of androgen receptor expression in a breast cancer tissue was also important with the -- enobosarm's anti-tumor activity, which is consistent with enobosarm being a targeted agent or a biomarker that could select or enrich for subjects who are most likely to respond to enobosarm therapy. AR sustaining status will be a critical inclusion criteria in the Phase 3 clinical trial design. The subset analysis of AR staining, and enobosarm anti-tumor activity, from the Phase 2 clinical study, will be presented at the upcoming ASCO 2021 meeting on June 4 through the 8, and the presentation's entitled, Efficacy of enobosarm, a selective androgen receptor targeted agent, correlates with the degree of AR positivity in advance AR+ER+ breast cancer, in an international Phase 2 study. It will be presented by Professor Carlo Palmieri, Professor of Translational Oncology and Medical Oncologist at the University of Liverpool as a posted discussion session in the abstract numbers 10-20.

By targeting the androgen receptor, in ER+ metastatic breast cancer, enobosarm introduces a novel endocrine therapy to patients with breast cancer, that have exhausted ER blocking agents and CDK4/6 inhibitors, but prior to IV chemotherapy. In October of 2020, the company met with FDA to discuss the enobosarm clinical breast cancer program. The FDA agreed to the Phase 3 registration clinical trial to study design, to evaluate the efficacy and safety of enobosarm 9-milligrams versus an active control, either exemestane or SERM for third-line treatment of androgen receptor ER+HER2-, metastatic breast cancer patients, that have failed a nonsteroidal aromatase inhibitor, fulvestrant and a CDK4/6 inhibitor.

Phase 3 study will be called the ARTEST study and the primary endpoint will be median radiographic progression-free survival. We were intrigued by the preclinical study results reported in the recent Nature Medicine publication, I mentioned. And in that they showed that enobosarm in combination with a CDK4/6 inhibitor, restored the CDK4/6 inhibitor's ability to suppress the androgen receptor positive, ER+ metastatic breast cancer, that was previously resistant to both the estrogen receptor blocking agents and CDK4/6 inhibitors, which as you know, is the target population in the planned Phase 3 ARTEST clinical study.

We met with the FDA again in April of 2021 to discuss the Phase 3 ARTEST clinical study, and the best regulatory strategy to address the combination treatment of enobosarm CDK4/6 inhibitor in an AR+ER+HER2-, metastatic breast cancer patient, who has progressed following treatment with a CDK4/6 inhibitor and AR blocking agent. First, FDA was enthusiastic about the -- targeting the androgen receptor in AR+ER+, metastatic breast cancer, and requested we also have a companion diagnostic test for this important biomarker to identify the target population. Second, based on the FDA's regulatory guidance, Veru plans to conduct 2 separate enobosarm selective AR targeted programs.

Program one, is to evaluate enobosarm monotherapy in a third-line metastatic setting. We will conduct a Phase 3 registration clinical study to evaluate the efficacy of enobosarm monotherapy versus the active control, in this case exemestane or SERM, in subjects with AR+ER+HER2- metastatic breast cancer, who have failed a non-steroidal AI, fulvestrant and a CDK4/6 inhibitor, so this is the ARTEST clinical study. And it's in approximately 210 subjects, anticipated to commence in June of 2021.

Program 2, this is new, is to evaluate enobosarm plus a CDK4/6 inhibitor combination therapy, moving it earlier in a second-line metastatic setting. We will conduct a Phase 2 clinical trial to evaluate the efficacy and safety for enobosarm plus CDK4/6 inhibitor, abemaciclib combination versus an alternative estrogen receptor blocking agent whether it's fulvestrant or AI, they'll be active control in subjects with AR+ER+HER2- breast cancer, who have failed the first line, and first line in this case is palbo (sic) [palbociclib], the CDK4/6 inhibitor plus an estrogen receptor blocking agent.

The clinical study in approximately 106 subjects is expected to commence in calendar Q3 2021.

Now let's focus on the Phase 3 ARTEST trial, which is expected to start next month. The design is as -- more specifically as follows. An open-label, multi-center, multinational, randomized 1:1, active controlled pivotal study, evaluating the efficacy and safety of enobosarm 9-milligrams daily oral versus an active control which is going to be either exemestane or SERM, this will be the physician's choice, in centrally confirmed AR+ER+HER2- metastatic breast cancer subjects, who have failed a nonsteroidal AI, fulvestrant and a CDK4/6 inhibitor.

The primary endpoint is median, radiographic progression-free survival. The statistical assumptions are, estimated median radiographic free survival at 6 months for the enobosarm monotherapy versus 3 months with the active control, exemestane or SERM. With an alpha of 0.05 and 99% power and a 20% drop out rate, the sample size will be approximately 210 subjects. We expect enrollment to take 10 months recruitment time and 12 months follow-up after the last patient is dosed. We expect that the androgen receptor companion diagnostic test will be developed in parallel to the Phase 3 ARTEST study with a large diagnostic company partner. The Phase 3 ARTEST study will be conducted in 49 clinical sites across the United States, too excited to get going on this.

Next, I will update you on the Phase 2b clinical study evaluating sabizabulin for the treatment of taxane chemotherapy resistant metastatic triple-negative breast cancer. Metastatic triple-negative breast cancer is an aggressive form of breast cancer. It represents approximately 15% of all breast cancers. This form of breast cancer does not express the estrogen receptor, the progesterone receptor HER2, and is resistant to endocrine therapies. The first line of treatment usually consists of multiple systemic chemotherapies including IV taxane chemotherapy. Unfortunately, almost all of these women will eventually develop resistance and exhibit tumor progression. In preclinical studies of human triple-negative breast cancer that has become resistant to paclitaxel which is a taxane, sabizabulin significantly inhibits cancer proliferation, migration, metastases and invasion.

We plan to submit an IND using the safety information from the Phase 1b/2 sabizabulin prostate cancer clinical studies, plan to initiate an open-label 3-arm Phase 2/b clinical study, to evaluate the efficacy and safety of sabizabulin, sabizabulin plus TRODELVY combination versus TRODELVY alone, in the treatment of approximately 150 metastatic triple-negative breast cancer patients that have failed at least 2 systemic chemotherapies, including IV taxane. In human prostate cancer clinical trials, we've already shown chronic oral daily administration of sabizabulin was well tolerated with no reports of neutropenia. It will be interesting to see whether sabizabulin in combination with TRODELVY results in less neutropenia, with a better efficacy similar to what has been observed in a metastatic non-small cell lung cancer trial with Plinabulin and IV [coltracine] tied targeted anti-tubing with a similar mechanism to sabizabulin, in combination with docetaxel, which is a taxane, prevented docetaxel induced neutropenia. The Phase 2b study is planned to commence in calendar Q3, 2021, and as I mentioned if successful, this would represent a second major clinical oncology indication for sabizabulin.

This week -- now moving to the COVID-19 study. This week, we expect to enroll our first patient in the Phase 3 COVID-19 study, evaluating sabizabulin for the treatment of hospitalized patients with COVID-19, who are at high risk for acute respiratory distress syndrome. Sabizabulin in this setting is a novel once-daily oral-dosed small molecule with both broad antiviral and anti-inflammatory activities, which may serve as a 2-pronged approach to the treatment of COVID-19 virus infection and the subsequent debilitating inflammatory effects that lead to ARDS and death. We conducted a double-blind, randomized, placebo-controlled Phase 2 clinical trial, evaluating once daily oral dosing sabizabulin 80-milligrams versus placebo in 39 hospitalized COVID-19 patients, who are at high risk for acute respiratory distress syndrome. The primary efficacy endpoint, with proportion of patients alive without respiratory failure at day 29, for the primary endpoint in hospitalized patients and modified intent to treat population, sabizabulin treatment compared to placebo had a clinically meaningful reduction in proportionate patients who are treatment failures dead or alive with respiratory failure, with a 30% treatment failure rate in the placebo group [n] equals 20, compared to 5.6% in the sabizabulin treated group n equals 18 at day 29. This represents an 81% relative reduction in the sabizabulin treated failures.

Secondary endpoint in the intent to treat population, sabizabulin reduced the proportion of patients who died on study from 30% in the placebo group to 5.3% in a sabizabulin treated group with a p-value of 0.044. This is an 82% relative reduction in mortality in the sabizabulin treated group. In an MITT population, sabizabulin showed a statistically significant and clinically meaningful reduction in days in the ICU, with sabizabulin patients at 3 days versus placebo at 9.55 days, p value 0.004. Sabizabulin reduced the days on mechanical ventilation for 5.4 days in the placebo group to 1.6 days in the sabizabulin treated group, and sabizabulin was tolerated with a good safety profile.

The company was granted an expedited end of Phase 2 meeting with FDA to discuss the next steps, including the Phase 3 clinical registration trial design for sabizabulin COVID-19 program. The FDA agreed upon sabizabulin for the COVID-19 Phase 3 trial as a double-blind, multi-center, multinational randomized 2:1 placebo-controlled trial, evaluating daily oral doses of 9-milligrams of sabizabulin for up to 21 days versus placebo in 300 hospitalized COVID-19 patients, who had high risk for ARDS. There will be 200 subjects who will be treated with sabizabulin and 100 subjects who will receive placebo.

Because of better oral bioavailability, the systemic blood levels in the 9-milligrams sabizabulin dosage is similar to the 18-milligrams sabizabulin formulation used in the Phase 2 study. Subjects in both the sabizabulin and placebo arms will also be allowed to receive standard of care. The primary efficacy endpoint will be proportion of patients that die on study up-to-day 80, so it's mortality. Secondary endpoints will include the proportion of patients without respiratory failure, days in the ICU, WHO ordinal scale for clinical improvement change for baseline, days on mechanical ventilation, days in the hospital and viral load. The study will be conducted in the United States, Brazil, Argentina, Mexico and Colombia, and enrollment is targeted to be completed by year-end. The company has sufficient clinical drug supply on hand to complete the Phase 3 clinical study. We will seek funding from the Biomedical Advanced Research and Development Authority of the U.S. Department of Health and Human Resources BARDA, and other agencies to try to fund the estimated amount of the commercial drug to supply the needs of the U.S. population, assuming confirmatory positive clinical results and FDA approval.

COVID-19 infection rates and hospitalizations are still at a serious level. There are mutating and double mutating virus strains, and large parts of the population either unwilling or unable to get access to effective vaccines. In fact, global cases of COVID-19 are at the highest level since the start of the pandemic. It is clear, that effective and safe oral therapeutic that can prevent deaths in hospitalized patients with moderate to severe COVID-19 disease, who are at risk for acute respiratory distress syndrome is desperately needed.

We strongly believe that sabizabulin with its anti-inflammatory and antiviral properties and its favorable safety profile can be greatly -- can be that greatly needed oral therapy. Based on the strength of these Phase 2 clinical study, promising clinical results, the company continues to be duty bound during this persistent global pandemic to pursue the COVID-19 indication, even though it's not our primary focus of the company. We believe we have the resources con -- to conduct our planned sabizabulin for COVID-19 Phase 3 trial without impacting the other cancer drugs in clinical development.

Finally, I'll comment on TADFIN. TADFIN is our combination tadalafil 5-milligram, finasteride 5-milligram, urology product, developed to treat low urinary tract symptoms caused by benign prostatic hyperplasia, also known as BPH. The combination product contains tadalafil, which is approved for the treatment of BPH and erectile dysfunction, and finasteride for BPH. We submitted the NDA for TADFIN to FDA in February. FDA accepted the NDA in April. Our PDUFA date decision -- or the -- yes, decision date for TADFIN will be December of 2021. We plan to launch TADFIN, If approved, via third-party telemedicine channels and when launched, it should - we should provide near term source of additional revenues for Veru. So we're not going to have a marketing and selling group, it will be done through telemedicine.

I will now turn the call over to Michele Greco, CFO and CAO, to discuss the financial highlights. Michele?

Thank you Dr. Steiner. As Dr. Steiner indicated, we're having a great year. In December, the company sold PREBOOST for $20 million, and in February, the company completed an equity raise which resulted in a $107.9 million in net proceeds after deducting underwriting commissions and costs. And to give you a sense of the continuation of our revenue growth trajectory, in the U.S. prescription channel, we sold 171,900 units year-to-date in fiscal 2020, compared to 247,200 units year-to-date in fiscal 2021, an increase of 44%.

I'll start our highlights with the second quarter results for the 3 months ended March 31, 2021. Overall, net revenues were up 34% to $13.3 million from $9.9 million in the prior year second quarter. The company reported record quarterly sales for its U.S. prescription business of $10.3 million, an increase of 48% from $7 million in the prior year second quarter. Overall, gross profit was $10.9 million dollars or 82% of net revenues, compared to $7.4 million or 75% of net revenues in the prior year quarter. The increase in gross profit and gross margin is driven primarily by increased sales in the US FC2 prescription business.

Operating expenses for the quarter increased to $12.4 million dollars, compared to the prior year quarter of $7.7 million. Research and development costs were $7.6 million, compared to $3.9 million in the prior year quarter. The operating loss for the quarter was $1.5 million, compared to $300,000 in the prior year quarter. Non-operating expenses were $1.4 million, compared to $644,000 in the prior year second quarter, and primarily consisted of interest expense and the change in the fair value of the derivative liability related to the synthetic royalty financing. We entered the synthetic royalty financing during March of 2018. For the quarter, we recorded a tax expense of $22,000, compared to a tax benefit of $133,000 in the prior year second quarter. The bottom line results for the second quarter of fiscal 2021 was a net loss of $2.8 million or $0.04 per diluted common share, compared to a net loss of $811,000 or $0.01 per diluted common share in the prior year second quarter.

Now turning to highlights for the results for the 6 months ended March 31, 2021. For the first 6 months of fiscal '21, total net revenues were up 36% to $28 million from $20.5 million in the prior-year period, a record high for the 6-month period ended March 31. The company recorded growth in the FC2 sales in the U.S. prescription business and in the global public sector business. Net revenues from the U.S. prescription business was up 49% to $19.4 million from $13 million in the prior year period. The global public sector business was up 11% to $7.7 million. Overall, gross profit was $21.7 million or 78% of net revenues, compared to $14.7 million or 72% of net revenues in the prior year period. The increase in profit and gross margin is due primarily to an increase in U.S. prescription business.

Operating expenses increased by $5.6 million to $22.4 million, compared to the prior-year period of $16.8 million. The increase is primarily driven by research and development costs, which increased by $4 million to $13.3 million from $9.2 million in the prior year period. Operating income for the period was $17.7 million compared to an operating loss of $2.1 million in the prior year period, an increase of $19.8 million. The increase was primarily due to the gain on the sale of PREBOOST of $18.4 million. Excluding this gain, we had operating loss of $694,000 for the period. Non-operating expenses were $3.2 million, compared to $2.2 million dollars in the prior year period, and primarily consisted of interest expense and the change in the fair value to derivative liabilities related to the synthetic royalty financing.

For the six month period, we recorded a tax expense of $100,000 compared to a tax benefit of $210,000 in the prior year period. The company has net operating loss carry-forwards for U.S. federal tax purposes of $41.7 million with $13.5 million dollars expiring in years through 2038, and $28.2 million which has been carried forward indefinitely. Our U.K. subsidiary has net operating loss carry-forwards of $61.3 million, which do not expire. The bottom line results for the first 6 months of fiscal 2021 was net income of $14.4 million or $0.18 per diluted common share, compared to a net loss of $4.1 million or $0.6 per diluted common share in the prior period. Excluding the gain on sale of PREBOOST, the adjusted net loss was $4 million or $0.6 per diluted common share in the current period.

Turning to our balance sheet. As of March 31, 2021, our cash balance was $136.7 million. Our accounts receivable were $5.1 million. Due to our sales PREBOOST we added $15 million in cash during December and $5 million in notes receivable, which will be collected over the next 15 months. In February, we completed an underwritten public offering of 7,419,354 shares of our common stock at a public offering price of $15.50 per share. Net proceeds were $107.9 million. Our net working capital was $137.2 million at March 31, 2021, compared to $12.3 million at September 30, 2020. During the 6 months ended March 31, 2021, we used cash of $1.9 million for operating activities, compared with $4.9 million dollars used for operating activities in the prior period.

Overall, we're delighted to see the continued increases in sales in the U.S. prescription business and look forward to increasing sales in the global public sector business in the third quarter. These revenue sources together with our strong balance sheet continue to be a source of funds we use to invest in our promising pharmaceutical clinical development program, as we continue to transform our company into an oncology biopharmaceutical company with the focus on developing novel medicines for the management of prostate and breast cancers.

Now I'd like to turn the call back to Dr. Steiner.

Thank you, Michele. Our company's fundamentals is strong. We've enjoyed another strong financial quarter with record U.S. FC2 prescription net revenues, which has allowed us to significantly advance our clinical programs. Based on year-to-date performance, we expect to have a record year in revenue. With the robust performance of the sexual health business, plus the prospects to additional future revenue from TADFIN, coupled with our strong cash position, we believe that we'll be able to substantially invest in the continued clinical development of our prostate and breast cancer drug product candidates as well as with sabizabulin COVID-19 Phase 3 clinical study. We plan to continue to generate robust growing revenues for the sexual health business.

As previously announced, the company also continues to explore strategic alternatives. regarding its legacy Female Health Company business, which markets the FC2 Female Condom, Internal Condom, including continuing to operate the business. It's been a very, very busy quarter as we have successfully transplant -- continue to transform our company into a late clinical stage oncology biopharmaceutical company supported by growing revenue from our cash generating sexual health business. We plan to enroll potentially up to 5 registration studies and 2 Phase 2 studies, this calendar year. More specifically, prostate cancer, sabizabulin in an open-label Phase 3 VERACITY study in men with metastatic castration and androgen receptor targeted agent-resistant prostate cancer, VERU-100 in an open label Phase 2, and later in the year, an open label Phase 3 for hormone-sensitive metastatic prostate cancer. For breast cancer, enobosarm in an open label Phase 3 ARTEST study in AR+ER+HER2- metastatic breast cancer in a third-line metastatic setting after failing a non-steroidal AI, fulvestrant and a CDK4/6 inhibitor. Enobosarm plus abemaciclib combination in an open label Phase 2 study in AR+ER+HER2- breast cancer -- metastatic breast cancer in a second line metastatic setting, after failing palbociclib plus an AR blocking agent. Sabizabulin, sabizabulin plus TRODELVY combination or TRODELVY alone in an open label Phase 2b study in metastatic triple-negative breast cancer patients, who have failed at least 2 systemic chemotherapies, including an IV taxane. And for COVID-19, sabizabulin 9-milligrams in a Phase 3 trial, double-blind, multi-center multinational, randomized, placebo-controlled trial in hospitalized COVID-19 patients who are at high risk of ARDS. And if we do confirm, the promising results that we observed in the completed Phase 2 clinical study, we expect to seek an emergency use authorization for this indication.

With that I will now open the call to questions. Operator?

(Operator Instructions) And the first question comes from Chris Howerton with Jefferies.

Congratulations on the very broad progress here to you Mitch and the team. For the -- for the 2 questions from me, first up, with respect to, excuse me, to sabizabulin. Could you give us just a little more color in terms of what the impetus was to reformulate the drug, in it's, sounds like a more bio availability dosage form? And then what additional operational work may be required to have that formulation fully ready to go for the upcoming clinical trials and of course commercialization? The second question that I have is related to AR expression levels and the potential for a companion diagnostic. So I guess, for that feature of the enobosarm development program, is the expectation that there will be some cut off of AR expression? And if so, or if not, will we learn --what we learn at the ASCO presentation with respect to that?

So the first question is on the reformulation. As you know, in drug development you typically start with the cheapest way to do this study and that is you take the drug and you put it just -- you pack it into a capsule, and that's what you give patients in the Phase 1b/2. So what we've done is, we -- the to-be-marketed form. So I've got to be careful because the (inaudible) will get mad when I say that. But the to-be-marketed form doesn't mean that we've got approved. It means that it's the form that we would use, if approved. And typically in your Phase 3, you have to use the form that is to-be-marketed so that you have your commercial form.

So the answer to your question, there is no further work. Serendipitously, when they put in the excipients and created the formulation for the Phase 3, and we did the PK study in the Phase 1b/2, it turns out that the excipients allowed for better oral bioavailability. And so that means that the 32-milligram dose is equivalent to the 63-milligram dose. And it raised the question that in the Phase 1b/2, where does the other 31-milligrams go? The answer is, the other 31-milligrams didn't disappear, it stays in the gut. And it may be responsible for some of the diarrhea that we're seeing, for example, even though it's Grade 1, Grade 2.

So one potential benefit of the reformulation is that we may in the Phase 3 setting see some fewer side effects, that would may be related to residual drug that was not absorbed. So, we don't have do any additional work. We have the to-be-marketed form, and that form is the one that we're going to be using not only in the Phase 3 for prostate, we'll be using it in the 9-milligram version in the Phase 3 for COVID-19, which will start this week, and we're using it also in the triple-negative breast cancer study, that has sabizabulin going against TRODELVY and in combination with TRODELVY. Second question has to do with AR expression.

This is exciting, because every so often you find somebody says they have a biomarker or a targeted marker, but this is truly a targeted marker. And what we're going to be presenting in the June ASCO meeting is -- are the data to support that. And as you would imagine, there is some expression level where you get better activity, because for something to be considered a targeted marker, it has to be -- for activities to happen it has to happen through that marker.

So in this case, you wouldn't expect activity with enobosarm if the andro (sic) [androgen] receptor is not present. And the second thing is, the more of that marker that's a bit -- that's being expressed, the better the result should be at least from and anti-tumor activity, and we see all that. And so, we're going to be presenting in the ASCO paper and ASCO presentation, is the data to support that, and particularly as it relates to objective tumor responses, target tumor responses, clinical benefit raise, radiographic progression-free survival, all goes to the right -- it all goes as expected -- as you would expect if AR's truly the reason why enobosarm is working.

And so because of that, it becomes critical that you have a companion diagnostic that can be done and it's immunohistochemistry, so it's not complicated, which is a good thing for us because we don't want a complicated companion diagnostic. One that can be easily done, can be done across the world, could that -- we don't want that to be the bottleneck, but to be able to identify women that are most likely to response -- respond and means that we can actually stack the deck in our favor, in the sense that we're going to be putting in women that will have a hopefully robust response to enobosarm, so that we can blow away the active control. That's the intent. And so, we're not a companion diagnostic company.

So for us to do something that's not in a wheelhouse doesn't make sense. We are in discussions with companies that -- once we announce those companies, you're going to say these guys know what the hell they're doing, and this -- and they will be able to work with us in parallel, so the companion diagnostic and the drugs are both available at the same time. And they've done this over and over, because this is -- we can do therapeutics, let them do the diagnostic. But having a companion diagnostic, it also is an opportunity for laboratories to when they -- breast cancer is one of those cancers that when a woman is diagnosed, she is automatically, molecularly characterized.

Meaning that they look for the estrogen receptor, the progesterone receptor, HER2 expression, in some cases BRCA1 and BRCA2. So the androgen receptor can be added in that very select group of initial molecular characterizations of the breast cancer. And the report says, by the way enobosarm's available. And you can't ask for better marketing than that, because then that -- we'll be the only one available for it. So, yes, you'll be learning at the ASCO meeting. You'll be seeing the cut-off, the correlations and all that stuff.

We're -- again, we're excited because this just helps us enrich our patient population for those patients. Now, the last question somebody may ask is, well, if you do that, are you reducing the number of patients so much that you've really reduced the number of patients in your market. Refresh your memory, 85% of women are going to be AR+ and of those women that -- even if we had half those, that's a huge population of women that will still be eligible for our AR targeted population. Compared to BRAC1, BRAC2 you're at 5% or 10%. We are going to -- its better -- I think from the standpoint of having a drug that works in majority of the time in a good number of patients would be -- would make sense.

Okay. I look forward to that presentation at ASCO.

Thank you, Chris.

And the next question comes from Brandon Folkes with Cantor Fitzgerald.

Congratulations on all the progress. Maybe firstly just -- what is your degree of urgency to fill the Female Condom business? Obviously, it continues to do well and well capitalized now, so just any color there. And then secondly, sorry if I missed this, but on the enobosarm Phase 2 combination studies, it starts next quarter, will this be a registration study?

Okay. Your first question, and it's kind of where we are with the Female Health Company business. So as we announced, we are in an again another record year. We had a record year last year, and this year it looks like it's heading that way again, and you can see from the numbers, it looks like any math you do, we're on it -- we are on a growth trajectory that is high growth.

And the other thing it's important to realize, is that the margins that we're receiving because we changed the business from a public sector business to a U.S. prescription business is as you would imagine is more like a prescription product. And as a result, it allows us to have -- and let me make one more comment, and because we're not selling the prescription product using a marketing and selling sales force of 70 people or 100 people, which is eating up -- it's your -- eating your profits, we spent almost no money on marketing and selling.

So essentially, all of that money can be reinvested into our projects. That's why we're able to run all of these projects and our cash is strong. And so, I think the shareholders want us to be able to invest in with multiple shots on goal in these billion dollar opportunities. And to be able to have this foundation, this platform to do that is wonderful. We are very blessed and we're very excited that the team has been able to do this. With that said, the best time to look for a possible alternative strategy to monetize the business, is when it's doing well, and it's growing.

The flip side of it is, when it's doing well, and it's growing, it takes a lot of pressure off the company, because you're not trying to do a fire sale. You want it to get -- you want to get the best deal that you can get. Interestingly, by doing a successful fundraiser that we did, back in February, it put enough resources in the bank, that we're also in a position that we don't have to take any deal that comes in, for the Female Health Company, because we have to -- we have the resources to keep going.

So I think we've put ourselves in the best position to monetize this at the best price for shareholders, and not put ourselves in any time strain or any -- I mean we're in the driver seat. So from that standpoint, what I can tell you is, there is a lot of activity and we continue to explore all kinds of options, and because we're not stressed for time, because we have the money, and we're moving forward, we're going to do this in a way that's best for the shareholders.

As it relates to your second question, which is enobosarm's second indication, second -- it actually is a second indication. The FDA said you can do a combination therapy. There's a lot of things you have to do with combination therapies, and that first is to make sure that there's safety in the combination therapies. That's really a separate program. So, we decided that based on the FDA's response, that the easiest thing to do is enobosarm monotherapy in a third line setting. We have the data, we've treated heavily pre-treated women that have failed estrogen receptor blocking agents and 12% failed CDK4/6 inhibitors, you see good activity, preclinical data.

So we're good to go with our test Phase 3. But boy, wouldn't it be nice to move in earlier in a second-line setting? So that means if 83% of patients are coming in with ER+ breast cancer, and they're getting treated with a CDK4/6 inhibitor, which almost predominantly is palbo -- palbociclib, and an estrogen receptor targeted agent with a non-steroidal AI or fulvestrant, what did you do after they fail?

So that -- we -- initially we were told this is a crowded space, there's a lot of drugs trying to get in this space. But literally, overnight because of CDK4/6 inhibitors, that crowded space has become less crowded, because of the fact that, after first-line therapy, the majority of women are looking for something that has not been proven. So the Phase 2 that we're doing is -- it's not a -- we're not thinking of it as a registration trial, we're thinking the Phase 2 in a second-line setting, is to provide us the information we need to confirm it in a Phase 3 study.

Congrats again on the progress.

Thank you.

And the next question comes from Leland Gershell with Oppenheimer.

Thanks for the comprehensive update on all your plans. Just a quick question, just really a clarification. The exploratory arm with CDK4/6 inhibitor that you had contemplated for that ARTEST study is no longer going to be included in ARTEST, correct? Your CD 4K combination will be restricted only to the Phase 2 or will you be keeping that exploratory in the Phase 3 as well?

No, no. We moved the exploratory arm out of the Phase 3, so the Phase 3 then becomes simpler, easier, and as you know, every time we add an additional arm, it's another statistical hurdle. So the idea was just make it clean, do enobosarm monotherapy versus another estrogen receptor blocking agent which these women have failed (inaudible) And so it's a good control for us to go up against, and third-line setting, these women would have exhausted all these things.

And so it's a good -- it's pre-chemo and our side effect profile looks pretty good. It looks like an endocrine therapy, it's not a chemotherapy. There's no diarrhea, vomiting and hair loss, and all that stuff. And so, we feel that that's a great spot for us to be. But to move in earlier, that was our thinking, if we can do combination therapy. Because one of the things the agency asked for is that if you pick -- if you can do combination therapy, you just can't say I'm going to do CDK4/6 inhibitor and an estrogen receptor blocking agent. They want you to specifically name CDK4/6 inhibitor.

That makes sense, right? Because if you look at the CDK4/6 inhibitors, palbociclib has a different safety profile than for example ribociclib. And so, the one of the reasons why palbo's used so much and is the leader, is because of its safety profile and because it was first to market. So that's why in the Phase 2 -- in the combination program, which in the Phase 2, we're very specific, since that palbo's being used 80% of the time in first-line, then we're going to come in with a [vemociclib] plus enobosarm, and go up against -- what is standard-right now, which is another estrogen receptor blocking agents, and that -- my god, can you imagine if we were in the second-line setting? And moving over earlier.

So they are very separate programs, a Phase 3 program for third-line setting, Phase 2 program to go in earlier. And I think we'll get a lot of credit for good Phase 2 data, because then, at that point it's just going to confirming it your Phase 3. So essentially, what we've done is, we just increase the depth and breadth of the enobosarm program, and there'll be other indications that we'll be able to go into, that we'll announce later. But when you're the only game going after the receptor, which is there in some cases more prevalent in the estrogen receptor for breast cancer, then we have to continue to explore how we're going to build the indications for the drug.

And then just a follow-up. With the tolerability of enobosarm, any thoughts on a maintenance type use pattern down the line? Patients who may get through an initial treatment period and then they can stay on it, as a maintenance? Do you have any thoughts there?

So you're talking about in the trial or are you talking about real life?

No, no, no, real world.

Yes. So in the real world, since we're using radiographic progression-free survival as the endpoint, then the patient gets to stay on until they progress. So it won't be like induction chemotherapy followed by maintenance chemotherapy, because it's an endocrine therapy. How is it any different than tamoxifen being used for 5 years or an aromatase inhibitor being used for 3 to 5 years.

So, if we're fortunate, the treatment would be alongside the patients for as long as the patient is stable or benefiting from it. And so, we don't have to do any maintenance studies, it will be, they'll continue to take until -- it's almost similar to some of the cytostatic drugs like the tyrosine kinase inhibitors, where patients on it for a while, even in lung cancer.

And the next question comes from Kumar Raja with Brookline Capital Markets.

With regard to COVID-19 trial, and given the variability in standard of care with regards to different regions, how do you think that is going to impact the results? And also, looks like you are going with a 60-day endpoint in the Phase 3 compared to the 29 day. What are the factors driving this? Yes, so the first question has to do with recruitment and potential effect -- recruitment geography and potential effect on results.

So from that standpoint, in the United States, we still have several sites in U.S. that we're opening up and -- the United States is weird. It's become almost like a checkerboard, where some areas look fine and some areas are not fine. Even though we think we're getting out of it in the U.S., if you look at it, we're still between 39,000 and 50,000 cases a day, and you still have a death rate that is significant.

So I don't know how long that's going to go, but we're in position, given the Phase 2 to take advantage of that in the U.S. Now, one of the reasons why we picked set ICU days and all that stuff, which we were going to measure, we picked mortality. If you told me, why did you pick mortality, we picked mortality because you can't fake a death. So the patient dies, you can count that pretty easily. If a patient has respiratory failure, is a respiratory failure because of standard of care, is a respiratory failure because you couldn't get oxygen, is it days in the hospital because they needed that bed because there were sicker patients.

There's too many other variables that go into some of these other endpoints that people using the COVID-19 studies. Since we're going after hospitalized patients with WHO score of 5 or greater, by definition, these are the sickest patients and death is a pretty good endpoint to determine whether your medicines work -- is working or not. So even if you go into other geographic locations like Brazil, Mexico, Argentina and Colombia, as I mentioned -- and the hospitals, by the way, in those countries, are good enough, and we think that -- and again, of course, the FDA will always make you look at each region and how it contributes.

But we think we'll be okay. We have some back up in Europe. As you know, Europe is about to go through another surge. And so, we do have backup because if we need to, we're going to be incredibly aggressive and they can sure refill this trial by year-end. And so, I think we're going to be fine because of the endpoint, in terms of different geographies, but we will look at each geography and their contribution to the final answer at the end of the study. As it relates to 60 days versus the 29 days, looking at a mortality endpoint, we picked 29 days because the FDA picked 29 days, and if you look at almost every study that was done contemporarily, it was 29 days.

It turns out that we want to capture as much good information as we can, and what we've learned in our study is, if patient -- if patients were not doing well, you're going to capture most of them by day 29. But boy oh boy, it will be nice to see whether or not we have a benefit beyond that. And so day 60 is really what was -- in our previous study our safety window. So the idea is, if you capture it for 60 days, and death is an endpoint, and a patient is in respiratory failure, and they were able to keep them alive a little bit longer past day 29, but then he dies at day 35 or day 40, and he's in a placebo group, you want to capture that. I think what it will do is it will make the mortality data more robust.

And then next question comes from Yi Chen with H.C. Wainwright.

Just to clarify, is this the first time for the 9-milligram, the 32-milligram dose formulation of the sabizabulin to be used in their respective patient groups?

Yes, so it will be the first time for those formulations, but those formulations were bridged with a PK study that we did in the Phase 2 study in prostate, where we looked at the 63-milligram dose blood levels compared to the to-be-marketed Phase 3 dose forms.

And based on those data, which showed bio availability was 100% better than what it was before, then we went to the agency and the agency reviewed the formulations and agreed that the doses that we picked for the Phase 3s were acceptable, given what we've learned in the PK study in the Phase 2. So the answer is, yes, it's the first time we're using those formulations. But we also know -- we know what the drug levels are going to be and that drug level is going to be consistent with what we did in the Phase 2's. So the 9-milligram will be similar to the 18-milligram for COVID-19, and the 32-milligram is similar to the 63-milligram dose that we used in the Phase 1b/2 prostate.

Got it, thanks. My second question is, how are the operating expenses going to trend with multiple trial initiations throughout the year?

I lost your first part of your question. Say it again, please.

How are the operating expenses going to trend with multiple trial initiations?

Good question. So, Michele, do you want to answer that question?

Sure. We've indicated that our drug expenses increased for this period. Let me just pull those numbers there. Our R&D expense went a quarter from $3.9 million last year to $7.5 million, and for the 6 months then $9.2 million to $13.5 million. They're going to continue to increase. Again, this quarter, we were at $7.5 million, we're going to continue to increase those, as we continue to add all these trials that Dr. Steiner just went over on the call, that will be going on and being added over this calendar year. So they're going to continue to slowly increase.

Ladies and gentlemen, this concludes our question-and-answer session. I would like to turn the conference back over to Dr. Mitchell Steiner for any closing remarks.

Thank you. I appreciate you joining us on today's call, and look forward to updating you on all our progress at the next investors' call. Thank you again.

Thank you. The digital replay of our conference call will be available beginning approximately noon Eastern time today, May12, by dialing 1 (877) 344-7529 in the U.S., and 1(412) 317-0088 internationally. You're be prompted to enter the replay access code, which will be 10154431. Please record your name and company when joining. The conference has now concluded. Thank you for attending today's discussion.