Earnings call: Daré Bioscience reports progress in women’s health treatments

Daré Bioscience, Inc. (DARE), a biopharmaceutical company, recently held a conference call to discuss its financial results for the second quarter and to provide updates on its product pipeline focused on women’s health.

CEO Sabrina Martucci Johnson highlighted the company’s development of innovative treatments, including XACIATO for bacterial vaginosis and first-in-category candidates Sildenafil Cream for female sexual arousal disorder and Ovaprene for hormone-free contraception.

The company reported a decrease in general and administrative expenses and research and development expenses compared to the previous year. It also received funding through a royalty monetization transaction and a grant agreement, which will assist in the development of DARE-LARC1, their investigational contraceptive.

Johnson emphasized the potential market for Sildenafil Cream and the ongoing Phase 3 study enrollment for Ovaprene at 20 sites across the US. Additionally, the company is advancing menopause-related programs and expects to provide updates on these as they progress.

Key Takeaways

• Daré Bioscience is developing XACIATO for bacterial vaginosis and first-in-category candidates like Sildenafil Cream and Ovaprene.
• The company has reduced general and administrative expenses and research and development expenses year-over-year.
• Funding has been secured through a royalty monetization transaction and a grant to support the development of DARE-LARC1.
• Sildenafil Cream has potential as the first FDA-approved treatment for sexual arousal disorder in women.
• Phase 3 study enrollment for Ovaprene is underway, with a goal of 250 participants for 12 months of product use.
• Daré Bioscience is also focusing on menopause-related programs and responsibly managing their capital.

Company Outlook

• Daré Bioscience aims to build shareholder value through the development of innovative treatments for women’s health.
• The company is focused on advancing Ovaprene and Sildenafil Cream as their priorities.
• CEO Sabrina Martucci Johnson expressed optimism for the rest of 2024, with expected milestones and updates on various studies.

Bearish Highlights

• There were no specific bearish highlights mentioned in the call.

Bullish Highlights

• Daré Bioscience has a deep pipeline of products in development, with significant interest in their menopause programs.
• The company’s unique model positions it to accelerate innovation for women’s health and drive value for stakeholders.

Misses

• No specific misses were discussed during the earnings call.

Q&A Highlights

• The CEO discussed ongoing interactions with the FDA for Sildenafil Cream and the enrollment progress for the Phase 3 study of Ovaprene.
• There is openness to further discussions with the FDA, but no confirmations have been made.
• Updates on menopause-related programs are expected as they progress.

Throughout the call, Johnson reiterated the company’s commitment to advancing their product candidates while managing capital responsibly. With the Phase 3 studies for Ovaprene and preparations for Sildenafil Cream’s Phase 3, Daré Bioscience is working towards addressing unmet needs in women’s health and creating shareholder value. The company anticipates providing more updates on their programs and is poised to make significant strides in the coming year.

InvestingPro Insights

Daré Bioscience, Inc. (DARE) has been actively involved in advancing women’s health treatments, as outlined in the recent conference call. However, a closer examination of the company’s financial health and market performance using InvestingPro data reveals some challenges and opportunities that investors should consider.

InvestingPro Data highlights that the company’s market capitalization stands at a modest $29.49 million. The revenue for the last twelve months as of Q1 2024 is reported at $2.82 million, which represents a significant decline of 71.83% compared to the previous period. This decline in revenue is a critical metric, especially for a development-stage biopharmaceutical company that relies on successful product development and market acceptance. Additionally, gross profit margins have been deeply negative at -668.35%, indicating that the cost of goods sold far exceeds the revenue generated.

On a more positive note, Daré Bioscience experienced a significant return over the last week, with a 1-week price total return of 8.7%. This short-term uptick in share price could indicate investor optimism following the company’s updates or other market factors.

InvestingPro Tips for Daré Bioscience suggest that the company is quickly burning through cash, which is a concern for investors considering the company’s need to fund ongoing research and development. Analysts also do not anticipate the company will be profitable this year, which aligns with the reported negative earnings per share of -3.81 USD. Moreover, the company’s short-term obligations exceed its liquid assets, raising questions about its ability to meet immediate financial liabilities.

For those interested in a deeper analysis, there are additional InvestingPro Tips available at https://www.investing.com/pro/DARE. These tips can provide further insights into the company’s valuation, debt levels, and expectations from analysts, helping to inform investment decisions.

In conclusion, while Daré Bioscience shows promise with its innovative product pipeline, the InvestingPro Insights suggest that potential investors should weigh the company’s financial challenges against the opportunities within the women’s health market.

Full transcript – Dare Bioscience Inc (DARE) Q2 2024:

Operator: Welcome to the conference call hosted by Daré Bioscience to review the company’s second quarter financial results and to provide a general business update. This call is being recorded. My name is Leonardo, and I will be your operator today. With us today from Daré are Sabrina Martucci Johnson, President and Chief Executive Officer; and MarDee Haring-Layton, Chief Accounting Officer. Ms. Haring-Layton, please proceed.

MarDee Haring-Layton: Good afternoon, and welcome to the Daré Bioscience financial results and business update call for the quarter ended June 30, 2024. Today, we will review our second quarter results and discuss developments and expectations for our pipeline and portfolio. I’d like to remind you that today’s discussion will include forward-looking statements within the meaning of federal securities laws, which are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Any statements made during this call that are not statements of historical facts should be considered forward-looking statements. Actual results or events could differ materially from those anticipated or implied by these statements due to known and unknown risks and uncertainties. You should not place undue reliance on forward-looking statements. Forward-looking statements are qualified in their entirety by the cautionary statements in the company’s SEC filings, including on Form 10-Q for the quarter ended June 30, 2024, which was filed today. I would also like to point out that the content of this call includes time-sensitive information that is current as of today, August 12, 2024. Daré undertakes no obligation to update any forward-looking statements to reflect new information or developments after this call, except as required by law. I will now turn it over to Sabrina.

Sabrina Martucci Johnson: Thank you. I always like to start our quarterly calls by taking a minute to remind those of you who may be newer to the Daré story of our purpose and our mission. We believe Daré is the only publicly traded company focused solely on women’s health, pharmaceutical product development broadly and we remain dedicated to advancing disruptive products for the health and well-being of women through clinical development, regulatory review and ultimately to market. Our commitment and focus is to improve health outcomes and the lives of women by leveraging the basic science and pharmacology that is understood about certain active pharmaceutical ingredients or marketed products to accelerate innovative treatments that women want and need by boldly addressing existing therapeutic gaps. We seek to optimize these treatments for our target indications to enhance outcomes, convenience and side effect profile or to address a novel indication, where the pharmacology is well suited, but has not previously been applied to the indication in question for women. We believe we have the broadest portfolio of potential high-impact first-in-category product candidates to improve the health and wellbeing of women, many of which have already demonstrated proof-of-concept and that our robust pipeline positions us well for the short, medium and long term. During our last update call, we discussed the strides we made last year to advance innovative therapies for women and the key milestones anticipated for 2024. In addition to the continued commercialization of XACIATO, clindamycin phosphate vaginal gel 2%, the first FDA-approved product to emerge from our portfolio and a treatment for bacterial vaginosis in females aged 12 and older, that became available nationwide by prescription earlier this year via our collaborator Organon. We also discussed anticipated milestones focused on our first-in-category product candidates related to continuing to progress toward a Phase 3 trial of Sildenafil Cream, 3.6%, which has the potential to be the first FDA-approved treatment for female sexual arousal disorder, for which there are no FDA-approved treatments and continuing to enroll in our Phase 3 study of Ovaprene, our potentially first-in-category hormone-free, monthly intravaginal contraceptive candidate. Today, we’ll review our progress against the anticipated milestones for Ovaprene and Sildenafil Cream with a focus on providing context and metrics that are important to understanding the potential impact of these programs. We’ll also highlight today the status of and what comes next for our two product candidates in the menopause space, our monthly vaginal hormone therapy for hot flashes and our hormone-free vaginal insert for sexual pain. Before I do, I’m going to first turn the call back over to our Chief Accounting Officer, MarDee, to review our second quarter financial results.

MarDee Haring-Layton: Thanks, Sabrina, and thanks, everyone, for joining us today. I would now like to summarize Daré’s financial results for the quarter ended June 30, 2024, which I will refer to as the second quarter. As Sabrina mentioned, Daré’s business strategy is to assemble and advance a portfolio of differentiated product candidates that address meaningful unmet needs we’ve identified in women’s health and then to monetize the value of our portfolio’s clinical and regulatory advances over the near and long term. The investment required to build and advance a portfolio includes corporate overhead portfolio acquisition and maintenance costs and ongoing research and development or R&D expenses. During the second quarter of 2024, our general and administrative expenses, or G&A, were approximately $2.4 million, which is a 16% decrease compared to Q2 2023 due primarily to reduced head count and reduced professional services expense. Our R&D expenses, which vary from period to period based on clinical, preclinical manufacturing, regulatory and other activities across our entire portfolio were approximately $4.9 million for the second quarter, which is a 19% decrease compared to Q2 2023. As we guided previously this year, we continue to anticipate our full year 2024 R&D expenses will be less than our 2023 R&D expenses. Our comprehensive income for the second quarter was approximately $12.9 million driven by proceeds from the royalty monetization transaction we closed in April. We ended the second quarter with approximately $16.4 million in cash and cash equivalents and had approximately 8.5 million shares of common stock outstanding as of August 9, which reflects the reverse stock split that was implemented on July 1, 2024. In April, we announced and closed a royalty monetization transaction with XOMA in which Daré received $22 million in gross proceeds and following a prespecified total return to XOMA, XOMA will make upside sharing milestone payments to Daré equal to 50% of all remaining cash flows for XOMA under the transaction. This monetization of future net royalty and net milestone payments accelerates potential cash flows from the future commercial success of XACIATO and ensures that Daré and our shareholders have the opportunity to participate meaningfully in XACIATO economics, as commercialization progresses. This nondilutive financing provides Daré with a significant capital to help achieve our objectives and importantly, allows us to focus on advancing our late-stage potential first-in-category investigational products, Ovaprene and Sildenafil Cream, both of which represent large market opportunities. The structure of this transaction also underscores the significant potential of Ovaprene and Sildenafil Cream, with Daré retaining the significant majority of future economics and the ability to achieve attractive margins through retained net sales and all commercial milestones. In the second quarter, we also received $1 million as the latest installment under our grant agreement with a foundation in support of our investigational contraceptive, DARE-LARC1. Under the terms of the grant agreement, Daré may receive a total of up to approximately $49 million to support nonclinical development of DARE-LARC1. This funding will allow us to advance the development of DARE-LARC1 through nonclinical proof of principle studies and other work to prepare for the submission of an investigational new drug application with the FDA, approval of which is required to begin testing in humans. To date, Daré has received approximately $29.3 million under the DARE-LARC1 grant agreement. Together, the royalty financing and latest installment in grant funding represent our commitment to being creative, collaborative and opportunistic in seeking capital needed to meet our objectives and to build shareholder value. We encourage investors to review the more detailed discussion of our financials, our financial condition, liquidity, capital resources and Risk Factors in our Form 10-Q for the quarter ended June 30, 2024, which we filed this afternoon as well as our annual Form 10-K for the year ended December 31, 2023, which was filed on March 28, 2024. I’d now like to return the call back over to Sabrina.

Sabrina Martucci Johnson: Great. Thank you, MarDee. I’m now going to talk through our 2024 accomplishments to date and anticipated milestones with the focus on our late-stage candidates, Sildenafil Cream and Ovaprene. But first, I’ll provide an update on our on-market asset, XACIATO. So as a reminder, XACIATO or clindamycin phosphate 2% vaginal gel is indicated for the treatment of bacterial vaginosis in female 12 years of age and older. It’s a colorless single-dose vaginal gel that can be applied at any time of day and it’s formulated with the goal of limiting leakage and increasing vaginal retention time, not as time spent in place. In the first quarter of 2024 through our commercialization agreement with Organon, XACIATO became available by prescription across the United States. The Organon women’s health sales team continues to see steady month-over-month increases in total prescriptions of XACIATO and new prescriber volumes in line with the opportunity for a new branded entrant in the category. There are positive signals related to strong clinical acceptance among early adopters with multiple uses among trialists paired with a positive patient reception, and the team continues to unlock access channels for a frictionless fulfillment experience for both patients and providers. I’d now like to provide an update on Sildenafil Cream 3.6%. So during the second quarter, we continued our interactions with the FDA on the development program for Sildenafil Cream as a treatment for female sexual arousal disorder, including with respect to the proposed efficacy end points to take forward into Phase 3 development. The patient population and the endpoints we proposed to the FDA for Phase 3 clinical development were those where our post-hoc analyses for the Phase 2b study data showed that Sildenafil Cream demonstrated statistically significant and meaningful patient improvements. During the second quarter, we provided responsive materials to queries from the FDA regarding patient reported outcomes and the qualitative assessment of within patient clinically meaningful improvement that we saw in the Phase 2b study based on the participant exit interviews. While the FDA had indicated an anticipated providing additional feedback during the second quarter on the Phase 3 design, which would be the first ever Phase 3 pivotal study of a therapeutic candidate for the treatment of arousal disorder in women. Its review is ongoing, and we look forward to providing updates on the FDA’s feedback, the Phase 3 study design and plans as well as any relevant updates on our collaboration strategy as they become available. In preparation for Phase 3 initiation during the second quarter, we completed the bid defense meetings with the CROs being considered for the Phase 3 studies and launched the manufacturing campaign to support Phase 3. In terms of market and revenue potential, there are currently no FDA-approved treatments for any form of sexual arousal disorder in women, meaning Sildenafil Cream has the potential to be the first. Sildenafil is the active ingredient in tablet form for oral administration currently marketed under the brand name Viagra for the treatment of erectile dysfunction in man, which was undoubtedly one of the most successful prescription products ever launched and market research suggests that approximately 20 million women in the US experience symptoms of low or no sexual arousal. In terms of probability of success, we’ve already demonstrated that Sildenafil Cream increased genital blood tissue flow in quantitative studies, and as we previously shared, we’ve completed all of the study analysis and data from the exploratory Phase 2b RESPOND clinical trial of Sildenafil Cream, and identified the patient population that received the greatest benefit from Sildenafil Cream in their general arousal response. The efficacy findings and details regarding this patient population were published in the Journal of Obstetrics and Gynecology, which is the official journal of the American College of Obstetrics and Gynecology or ACOG and were available open access online in June, and our publication was featured as a featured article in July in the green room, which is the ACOG podcast. Our study was also spotlighted in an editorial in the journal. It’s a distinct honor to be featured and we are pleased to see the medical communities still engaged in these first of its kind data ran such a significant unmet need. We look forward to providing additional updates on the development program as they are available. In terms of Ovaprene, we also want to provide an update on the advancement of the Phase 3 study of Ovaprene, which is our novel investigational hormone-free monthly intravaginal contraceptive whose US commercial rights are under a license agreement with Bayer (OTC:). Non-hormonal contraception represents a significant commercial market opportunity as there are no currently no monthly hormone-free contraceptive approved by the FDA. Ovaprene has potential to be a disruptive product in the contraceptive category and an important option for women who cannot use hormone-based birth control products or prefer not to do so. Based on market research, approximately 35 million women in the US are potential candidates for Ovaprene. Working with study collaborators at the Eunice Kennedy Shriver National Institute of Child Health and Human Development or NICHD of the National Institutes of Health or NIH, we commenced patient enrollment in the Ovaprene pivotal Phase 3 clinical study in December of 2023. Recruitment is currently underway at 20 sites across the United States and it’s supported by a central advertising campaign for the study that launched in March of this year, March 2024. You can see the campaign materials by visiting our website homepage. While there are 20 sites currently recruiting, it’s clearly that a subset of approximately half of those sites are the most successful in translating into study participants that considerable interest we have seen from women in response to the central advertising campaign. As a result, we have a range of enrollment projection that vary considerably based on the enrollment rates at almost successful sites versus those that are not enrolling at a similar pace. As a reminder, the study aims to enroll sufficient participants across the study sites to have approximately 250 participants complete approximately 12 months, which is 13 menstrual cycles of product use. Based on the current average enrollment rate across all of the 20 sites, we anticipate that approximately 125 women, which is half of our target number of participants to complete the study will complete approximately six months of product use by the end of the second quarter in 2025. We are, of course, looking at strategies to ensure that all of the study sites are equally successful and productive and look forward to providing updates on enrollment projections and rates as enrollment progresses in the coming quarters. Based on communications to date with the FDA, if successful, we believe that just the single registration study will be required to support a premarket approval application submission with the FDA. I’d now like to turn to DARE-HRT1 and DARE-VVA1. Because lastly, given the unveiling earlier this year of the bipartisan Senate bill that would authorize $275 million to boost research training and public awareness around menopause and midlife women’s health issues, an area that has often been too stigmatized overlooked and underfunded, we’ve been getting lots of questions about our menopause-related programs. There, HRT1 is a potential first vaginal monthly therapy for the vasomotor symptoms of menopause. This is a program we are preparing for the single Phase 3 clinical study, we believe will be required for approval via the FDA’s 505 (b) (2) pathway. In addition, DARE-VVA1, which is our hormone-free vaginal candidate for sexual pain due to the vulvovaginal atrophy or VVA associated with menopause is Phase 2 ready, and we’re actively exploring opportunities to move this program forward. We’re looking forward to seeing continued progress in the menopause space and potential progress of this new bill, and will provide updates on our DARE-HRT1 and DARE-VVA1 programs as available. In summary, we continue to progress our portfolio of potential first-in-category product candidates and look forward to providing more updates this year as we work to advance some of the most potentially disruptive candidates for the health and well-being of women in decades, collaborating with leading companies, including Organon for XACIATO and Bayer for Ovaprene to commercialize and deliver these treatments to as many women as possible. I’d now like to turn the call over to the operator for Q&A.

Operator: [Operator Instructions] Your first question comes from the line of Catherine Novack of Jones Research. Please go ahead.

Catherine Novack: Hi, good afternoon. Congrats on all the progress this quarter. I wanted to ask again for Ovaprene. With the timing updates that you gave today can you give us a sense of what implications this has for top line readout? And then given that this is a single arm, do you have any plans for an interim look so we can see data a little bit sooner?

Sabrina Martucci Johnson: Yeah, absolutely. Those are great questions. You don’t have timing yet for top line. As I mentioned in the prepared remarks, there’s a difference in enrollment rate between some of the sites. And I want to be clear, there’s not a difference in demand. So the central advertising campaign has been quite successful in terms of generating patient interest in the study, quite equitably across the sites. It’s just a difference in terms of how successful some of the sites are translating those women into study participants from that considerable interest. And so we feel comfortable at this time, projecting when we’ll have, right? Half of the subjects having completed about halfway through, right, six months of their assessment. We definitely look forward to giving more updates, including an opportunity to do an interim analysis at that point, but we’re not prepared yet to give exact timing on final top line. We really want to get a little further in enrollment. And a little further in looking at some of these strategies we’ve been implementing to help all the sites be equally successful and productive in pulling those patients that have expressed interests forward.

Catherine Novack: Great. And then again, from just a single arm, can you remind us the typical use Pearl Index that you — that would make this commercially compelling asset?

Sabrina Martucci Johnson: Yeah, it’s a great question. So the nonhormonal category for — first I should take a setback. So Pearl Index is how contraceptive methods are evaluated by the FDA and it’s the metric that’s used regardless of whether it’s a hormonal product or a non-hormonal product and FDA-approved products have the very wide range of Pearl indices. So most effective is 1 that’s like an intrauterine device, right, which is implanted and the least effective of the FDA-approved methods are the spermicides or vaginal gel, which have a Pearl Index in the 27 to 28 range. So it’s a very broad range. And in the non-hormonal category, there really are not that many options and the options that are available, other than the IUD, which is in that one range, the other options are at the other end of the spectrum, closer to the 27 to 28 or the 27 to 28 range. So as we think about a product like Ovaprene, it would be the first product to be a once a month. So all the other nonhormonal products have been in the copper IUD are pericoital meaning they’re used in the method, think condoms, think [bromicide] (ph). So it would be different in that regard. And based on the pre-pivotal study data that’s been generated, that study suggests that the surrogate markers achieved for that study in contraceptive effectiveness that it has the potential to be in the same range as the hormonal methods, the short-acting hormonal methods like pills, patches, rings, but the bar is fairly low, right, for the non-hormonal methods given what some of the other approved products are. And that really means from an acceptability perspective, there’s really a wide range of efficacy that could be very acceptable for a method like Ovaprene, given that it also has convenience that none of the other nonhormonal methods have. So the pre-pivotal data suggests that it has that opportunity for effectiveness in the same range as the short-acting or hormonal method. And then to your question, Catherine, the range in general, though, for non-hormonal methods is actually quite wide, which really speaks to, in the end, it’s all about contraceptive methods that women will use, and that’s why the FDA has approved such a wide range of contraceptive effectiveness. So there’s a wide range, therefore, of acceptability and commercial viability for a product like Ovaprene, particularly given that it would be the only once-a-month method that’s available, right, non-pericoital method or non-implanted method that would be available in the hormone-free category.

Catherine Novack: Great. That’s helpful. Looking forward to getting more updates on the program down the line.

Sabrina Martucci Johnson: Absolutely. Thank you.

Operator: [Operator Instructions] Your next question comes from the line of Douglas Tsao of H.C. Wainwright & Co. Please go ahead.

Douglas Tsao: Hi, good afternoon. Thanks for taking my questions. Sabrina, in terms of your interactions with the FDA for the Sildenafil Cream program, I guess, I’m just curious, are you anticipating another meeting being needed to sort of get this final alignment or do you think your sort of interactions are sufficient to get this settled?

Sabrina Martucci Johnson: Yeah, that’s a great question. It’s definitely clear that, which we know, right, this is the first-in-category indication and a first-in-category product. And there’s a lot of data for the FDA to go through. And there’s also a lot of kind of key opinion leader support that we have provided to the FDA historically right, in terms of understanding of the indication, understanding of the outcome measures. So there may be questions or circumstances where that’s helpful. Not clear at this time. Right now, the questions have really been straightforward in terms of kind of the typical things. We’re providing a lot of, as I said, information around those outcome measures and what’s a clinically meaningful improvement, and there’s a whole very specialized assessment in the patient-reported outcome world called the psychometric analysis and assessment that was done. So a lot of the information we’re providing is really providing that color. But to be determined, we’ll definitely be open to that. We, to date, have had a number of meetings with the FDA. And when we’ve had them in the past, they’ve definitely been super productive. So we’re definitely open to that. But at this point, nothing definitive in that front.

Douglas Tsao: Okay. And just — you obviously have a very rich pipeline with a lot of opportunities. I guess how are you thinking about sort of prioritizing things in the context of your balance sheet and what you can afford to do right now?

Sabrina Martucci Johnson: Yeah. Another great question. So as we’ve really been trying to highlight Ovaprene and Sildenafil as our two either in Phase 3 as Ovaprene is or getting Phase 3 ready as Sildenafil is, those have really been our priorities, both operationally in terms of where we put our bandwidth, but also obviously, financially as well. And those really remain the priority. However, to your point, we have a very deep pipeline, in particular, with a lot of the noise around menopause lately. We’ve been getting a lot of questions and interest broadly around our menopause programs that we have, the two that I highlighted today. So we’re also doing everything we can to make sure that we are advancing those programs as much as possible operationally by being very capital responsible and really focusing our priorities around Ovaprene and Sildenafil right now responsibly with our capital.

Douglas Tsao: Okay, great. Thank you so much.

Sabrina Martucci Johnson: Absolutely.

Operator: That concludes our question-and-answer session. I would like to turn the call back over to Sabrina Martucci Johnson for any additional or closing remarks.

Sabrina Martucci Johnson: Great. Well, thank you all for taking the time this afternoon to hear about our recent updates and our ongoing commitment to drive value for all of our Daré stakeholders by identifying and advancing potential new therapies to provide additional choices, enhanced outcomes and ease of use for women. As you heard today, we continue to make great progress and are excited for what the rest of this year holds for Daré. As we look ahead to the rest of 2024, we expect several milestones this year, including more of a pre-pivotal study updates as they indicated, as we work to complete what we expect to be that single registration study, and as we’ve just been talking about, updates on our discussions with the FDA and the activities that we’re doing to commence that Phase 3 for a potential first-in-category treatment option for women with sexual arousal disorder, Sildenafil Cream. And as we also touched at the end of the call, our unique model really also has deep pipeline in support of commercial collaborators. And therefore, we believe we’re well positioned to accelerate innovation for women everywhere while also driving value for all of Daré stakeholders. We look forward to keeping you updated on our progress towards the milestones we discussed today. Thank you.

Operator: This concludes today’s call. Thank you all for joining. You may now disconnect.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.