Daré Bioscience Q3 2023 Earnings Call Transcript

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November 9, 2023

There are 6 speakers on the call.

Operator

To the conference call hosted by Dare Bioscience to review the Company's 3rd Quarter Financial Results and to provide a general business update. This call is being recorded. My name is Chris, and I'll be your operator for today. With us today from Dare are Sabrina Martucci Johnson, President and Chief Executive Officer John Fair, Chief Commercial Officer and Lisa Walters Hofford, Chief Financial Officer. Ms.

Operator

Johnson, please proceed.

Speaker 1

Thank you. Good afternoon and welcome to the Dare Bioscience financial results and business update call for the quarter ended September 30, 2023. Today, we will review our Q3 results and Before we begin, 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 of the 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.

Speaker 1

You should not place undue reliance on Forward looking statements are qualified in their entirety by cautionary statements in the company's SEC filings, including our Form 10 Q for the quarter ended September 30, 2020 which was filed today. I would also like to point out that the content of this call includes time sensitive information that is current only as of today, November 9, 2023. Dare undertakes no obligation to update any forward looking statements to reflect new slides from within the webcast module. We've included these slides to provide some additional context to our portfolio that you may find helpful while you listen to the call. The slide deck is also available in the Investor Relations section of our website under Presentations, Events and Webcasts and will remain on the site for 2 weeks.

Speaker 1

As you know, our sole focus at Dare is women's health. Women's health products make up 27% of total Blockbuster products, While contributing to 35% of total Blockbuster sales and there continue to be many unmet needs in the market, We believe we have an exceptionally strong pipeline of product candidates that positions us well for the short, medium and long term. I'm excited to share today the recent strides we've made to advance innovative therapies for women with our most promising near term opportunities. Since the beginning of Q3, we have had several important achievements. First, we achieved our first Commercial milestone for Zaciato, which was the initial shipment of the product associated with the launch.

Speaker 1

2nd, we Shared additional positive data from our Phase 2b response study of Sildenafil Cream, which has the potential to be the 1st FDA approved treatment for any form of sexual arousal disorder in women. And 3rd, we made further progress toward patient enrollment for the anticipated start of our Pivotal Phase 3 study of Ovaprene, our potentially 1st in class hormone free monthly intravaginal contraceptive candidate. Overall, we continue to advance our key pipeline programs, each of which, if approved, represents a potential 1st line or first in category opportunity. Additionally, we are actively engaging our commercialization collaborators, including leading players in women's health, Organon and Bayer, as we steadily execute on our mission to accelerate innovative treatments that women want and need. I'll now provide an update on our potentially disruptive late stage candidates, Sildenafil Cream and Ovaprene.

Speaker 1

Then John will provide an update on Xatiado's launch and Lisa will review our financial results for the quarter ended September 30. So let's start with Sildenafil Cream, which is our investigational therapeutic candidate to treat female sexual arousal disorder or FSAD And female sexual interest arousal disorder or Additional updates from our Phase 2b response study results in preparation for our confirmed upcoming end of Phase 2 FDA meeting this year. Sildenafil, which is a PDE5 inhibitor is the active ingredient in a tablet or for oral currently marketed under the brand name Viagra for the treatment of ED or erectile dysfunction in men, which was undoubtedly one of the most Our Sildenafil Cream is an investigational proprietary topical treatment Cream formulation specifically designed to be used on demand at the time of sexual activity to increase blood flow to the genital tissue in women. If development is successful, Sildetafil Cream has the potential to be the 1st FDA approved product to treat Any form of arousal disorder in women. Women who experience no or low sexual arousal are bothered by and dissatisfied with their sex They're frustrated with their sexual problems.

Speaker 1

They experience guilt about their sexual difficulties And they are likely to feel sexually inadequate, inferior and embarrassed. Market research suggests that approximately 20,000,000 women in the U. S. Age 21 to 60 experience symptoms of low or no sexual arousal and approximately 10,000,000 women are considered distressed And actively seeking treatment. We believe this is a promising untapped market given the numerous equivalent products approved for men, not only Viagra, but also Cialis and LOVITRA to name a few.

Speaker 1

Last week, we announced additional positive data from our Phase 2b RESPOND study of Sildenafo Cream, having completed our study analyses in preparation for our upcoming FDA meeting. Importantly, these additional analyses indicate that we can use our Phase 2b study approach in Phase 3. Specifically, this means we can propose a Phase 3 study with the same co primary endpoint structure That we used in Phase 2b, which assesses arousal sensation and evaluates concerns related to the difficulties with sexual arousal. And 2, that we can propose that in the Phase 3 study, we evaluate Sildenafil Cream in a broader patient population of women that includes Not only women with arousal disorder only or FSAD, but also those with arousal plus desire disorder, otherwise stated as women with female sexual interest arousal disorder or FSI AG. This would be the first ever Phase 3 pivotal study of a therapeutic candidate for the treatment of arousal disorder in women and we remain on track for our end of Phase 2 meeting with the FDA this year.

Speaker 1

We look forward to keeping you updated on those developments. Now, I'd like to turn to Ovaprene. Ovaprene is our investigational, potentially 1st in category hormone free monthly intravaginal contraceptive. We have been working closely with our Phase 3 study collaborator, the National Institute of Child Health and Human Development or NICHD of the NIH on the pivotal study planned to start later this year. The pivotal Phase 3 study of evaprene is being supported By NICHD's contraceptive development program, which oversees the contraceptive clinical trials network or CCTN, which was established in 1996 to conduct studies of investigational contraceptives like Ovaprene.

Speaker 1

We remain on track to start enrolling patients this Q4 of 2023 and we will issue an announcement after the first patient is enrolled. As a reminder, the study is a multicenter, single arm, non comparative, pivotal Phase 3 contraceptive study of Ovaprene to evaluate its effectiveness as a contraceptive along with its safety and usability. Based on our communications to date with the FDA, If successful, we believe that only this single registration study will be required to support a pre market approval application submission with the FDA. We believe Ovaprene has the potential to be a disruptive product in the contraceptive category and potentially life changing for women who cannot take hormone based therapies such as some cancer patients or those who would prefer not to do so. In fact, survey data indicate that nearly 85% of women would prefer a monthly option with a lower hormone dose than the oral birth control pill.

Speaker 1

In addition to providing innovation as a non hormonal contraceptive, the clear differentiation And disruptive potential of Ovaprene is in its convenience and potential efficacy. Its convenience includes easily monthly use and self administration without requiring action at the time of intercourse with target efficacy approaching hormonal birth control methods. There are currently no FDA approved monthly hormone free contraceptives. And based on market research, Approximately 35,000,000 women in the U. S.

Speaker 1

Are potential candidates for Ovaprene. We see parallels to NuvaRing When it entered the market as the 1st monthly intravaginal hormonal contraceptive and to Mirena when it entered as the first hormone releasing intrauterine system. And Bayer, which commercializes Mirena, is a leader in commercializing contraceptive products in the United And they hold the U. S. Commercial rights to Ovaprene under a license agreement with us.

Speaker 1

In summary, I am very excited about Progress we've made on our late stage program since our last call in August. As the only company solely focused on developing women's health products, Dare is developing 1st in category products. Our investigational products are some of the most potentially disruptive candidates for women in decades. And we collaborate with leading companies to commercialize and deliver these treatments to as many women as possible. And as you'll hear from Lisa later on this call, we do all of this with thoughtful and efficient capital deployment And leveraging non dilutive sources of capital wherever feasible.

Speaker 1

I'll now turn it over to John to provide update on the Organon Xatiata launch as well as Ovaprene pre commercialization activities underway in collaboration with DARE.

Speaker 2

Thank you, Sabrina. As a reminder, zaciatto clindamycin phosphate vaginal gel is a lincosamide antibiotic for single dose Vaginal administration indicated for the treatment of bacterial vaginosis or BV in female patients 12 years of age and older in the United States. As many of you know, Organon recently launched Xociado. The product is in the channel as of last month and the initial focus in Q4 is on high BV prescribers in the U. S.

Speaker 2

Aligned to end of year product availability in select retail pharmacies. As we have communicated on previous calls, Organon's go to market strategy leverages the knowledge and experience of the established Nexplanon commercial team. Organon believes there's a roughly 90 5% overlap of healthcare providers who prescribe their contraceptive product Nexplanon that also have the potential to prescribe Xatiatto based on provider treatment patterns. And to drive product pull through, their skilled market access team is meeting with customers to review Xaciata. Because of the strong relationships the Organon sales team has with these healthcare providers, we expect them to be well positioned to detail Zaciato.

Speaker 2

Looking ahead to our Phase 3 trial initiation for Ovaprene, we are excited to begin Phase 3 study activities with our U. S. Commercial collaborator, Bayer. In parallel, our team has been collaborating with Bayer on key downstream commercial initiatives intended to ensure a seamless transition from clinical development to commercial introduction. These activities will help set the foundation to maximize the value of this disruptive technology.

Speaker 2

With that, I'll turn the call over to Lisa.

Speaker 3

Thank you, John, and thanks, everyone, for joining us today. I would now like to summarize Dare's financial results for the Q3 of 2023. For those of you who are newer to the story, Dare's business strategy is To assemble in advance a portfolio of differentiated product candidates that address meaningful unmet needs that 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 in Advancement portfolio includes corporate overhead, portfolio acquisition and maintenance costs, And of course, ongoing research and development or R and D expenses. So during the Q3 of 2023, Our general and administrative or G and A expenses were approximately $2,700,000 unchanged from G and A expenses recognized during the Q3 of 2022.

Speaker 3

Our R and D expenses, which vary from period to period based on clinical, Preclinical, manufacturing, regulatory and other activities across our entire portfolio were approximately 6 $700,000 and primarily reflects the costs related to the Sildenafo Cream Phase 2b clinical trial and manufacturing and regulatory affairs activities related to Ovaprene's planned Phase 3 study. While my comments have focused largely on our expenses, I should note that during the Q3, we also recognized license fee revenue of $1,000,000 under our global license agreement with Organon. Our comprehensive loss for the Q3 was approximately $8,300,000 We ended the 3rd quarter with approximately $13,900,000 in cash and and as of November 8, we had approximately 98,600,000 shares of common stock outstanding. So moving to the Q4 of 2023, under our license agreement with Organon, we will receive a $1,800,000 commercial milestone payment as a result of the first shipment of Xociado in connection with its launch in the U. S.

Speaker 3

During the quarter. Thereafter, we will receive tiered double digit royalties based on net sales as well as additional potential milestones of up to $180,000,000 over time. Now that the sales efforts have commenced by Organon, Dare will begin to recognize thrilled that Zaciato is now available in the U. S. And I look forward to reporting on Zaciato's progress in the months ahead for all Dare stake Alders?

Speaker 3

I started my remarks with a review of our business strategy, so it now feels appropriate to take a moment and review our financial Since our inception, we have made fiscal responsibility a top priority, maintaining a lean and focused team and managing our overhead costs closely. In the current challenging market, we have reduced costs and are exploring additional opportunities to reduce costs when appropriate and where appropriate, but seeking to do so without compromising our focus on investing and cultivating our leading product candidates. We are looking at a wide range of opportunities to fund our high quality portfolio, including more creative and innovative vehicles that other companies may not have access to. Based on conversations to date, we've been buoyed by the depth and advance of our portfolio and our pipeline, and we are actively pursuing options to raise capital. As we've said previously and as Rina just noted, we will endeavor to be creative, collaborative and opportunistic in seeking the capital needed to meet our objectives and to build shareholder value.

Speaker 3

Again, as a reminder, these include, but are not limited to, non dilutive grants similar to those that we have obtained to finance many of our We have explored and will continue to explore a variety of options to fund our operations, advance our candidates, monetize the value of our assets and build shareholder value. We encourage investors to read the more detailed discussion of our financials, Financial condition, liquidity, capital resources and risk factors in our Form 10 Q for the quarter ended September 3, 2023, which was filed today as well as in our annual report on Form 10 Q for the year ended December 31, 2022, which was filed on March 30, 2023. I would now like to turn the call over to the operator for Q and A.

Operator

Thank you. The first question is from Catherine Novak with Jones Trading. Your line is open.

Speaker 4

Hi. Good afternoon. Thanks for taking my questions. A couple on Ovaprene. First is, do you plan Issue periodic updates regarding enrollment and is it possible that we might expect to see updates on some of the efficacy endpoints potentially before the top line data readout?

Speaker 1

Hi, thank you for the great questions and thanks for asking about Ovaprene. Obviously, very excited that the study is starting. In terms of providing updates, that definitely is our intention. As we've as a reminder The study duration is 13 cycles, which is about 12 months. So that's how long the women in Study will be using ovaprene over the course of that period.

Speaker 1

And as we've guided in terms of how long the study will take beyond that, it really comes down to the enrollment rate. Great. So we do really want to keep people informed, as the study progresses. So that's definitely our intent. The first announcement you'll get is that 1st patient enrolled and then we do intend to keep people updated as enrollment progresses as we have information that is suitable for that.

Speaker 1

And in terms of providing data updates, that's really a fantastic Question as well, because as you probably noted in the comments, it is a non comparative study, which means everyone's on Ovaprene. Everyone gets Ovaprene in And in contraceptive studies, you're looking at pregnancy rates over time. Having said that, Right now, there's not necessarily a plan to disseminate Any data before the study is completed. However, that is something that certainly we are discussing with our collaborators at the NICHD who are collaborating with us on the study, in terms of the merits of doing that and whether or not there might be a situation where that makes sense. So we will keep you posted on that as well.

Speaker 4

Great. And can you remind me The estimated cost of this ovaprene study and to what extent it's already funded in some part by NICHD?

Speaker 1

Yes. So just as a reminder for everyone and thank you for asking the question so that we can do that, because it's kind of a nice position to be And to have a Phase 3 study starting that actually we already paid for. And so the way the collaborative research agreement works with the NICHD is we have already provided into an account basically under that CRADA $5,000,000 towards the cost of the study. And then obviously the NICHD is providing resources as well to cover the cost of the study. And right now, we're working through the contraceptive clinical trial network, which is the 20 sites that the NICHD works with on these types of studies.

Speaker 1

And so that's those costs and our Funding to the NIH was really based on our determination with them and our CRO partner that they work with on studies in terms of the anticipated costs and needs of the programs. Obviously, there's always a potential for us To provide additional funding, under circumstances, for instance, if we felt we wanted to add sites or things like that. But right now, the study is funded, for what is planned currently. It's obviously underway. And based on the funding that's been provided And also just the way the NICHD does their contracts, that really even and we actually touched on this And our 10 Q related to questions we might get about what happens if there's a government shutdown, even just the way they do their contracts, it kind of obligates the funds out through the Q3 of next year.

Speaker 1

So that's the plan right now with the study.

Speaker 4

Okay. That's helpful. And then if I can just get in one more on sildenafil cream. So as you're moving this product into pivotal studies, are you considering partnerships as you did with Ovaprene and Asciatto either regional All are U. S.-based and at what point do you think it makes sense to start having those partnering discussions?

Speaker 1

Yes. So as we noted upfront, we're very proud that we are in collaboration With some of the leaders in women's health including, Organon and Bayer. And as you've noted, we've entered into those partnerships in different times through different programs. So with Ovaprene, as you noted, we entered into that collaboration before the Phase 3 trial, whereas with Organon on Xatiata, we entered into that Collaboration after that product was taken all the way through registration. Every product is different.

Speaker 1

Obviously, I hope it's obvious given everything we've talked about today. Sildenafil Cream is a very interesting program. There is nothing approved for female sexual arousal disorder. And so given that, it's an interesting program. There's a lot of interest in the program from a lot of different stakeholders.

Speaker 1

As a company, we always look at what makes the most sense in terms of ultimately where can we build the greatest value for shareholders, Which I am myself a shareholder as well. So we look at all the different aspects and possibilities. And so as you've seen historically, we've considered Partnerships at different times in the trajectory of a program, as Lisa commented, strategic partnerships are certainly a non dilutive way of funding certain But we've also very much had a practice of we don't talk about those things in advance When the time is right and that partnership is in place and it makes sense and we would talk about it, that we obviously consider all the possibilities for every program And really look at all the ways that we can fund our portfolio to build value. And with something like Sildenafil Cream, given it's a first in category product and there are no FDA approved treatments, there's interest in a program like that. So we have so what's nice about that I should stress is it puts Dari in a nice position and being able to think about what makes sense for Dari and our shareholders.

Speaker 4

Got it. That's very helpful. Thank you. Thanks so much for taking my questions.

Speaker 1

Absolutely.

Operator

The next question is from Douglas Tsao with H. C. Wainwright. Your line is open.

Speaker 5

Sabrina, along those lines of Sylvanasil Cream in terms of seeking a partner, Has any of the sort of stakeholders that you've spoken with expressed interest in having a voice in Helping design the Phase 3 program, because obviously you did such a novel program And the clinical development program could go in a lot of different directions.

Speaker 1

Yes, another great question. And if I may take a step back on the Selenafil Cream program because I think as many people know and I know you know in particular Doug, like this is a first, right? The Phase 2b trial was the first ever study of its kind conducted in this patient population. And as a result, Dare had to do a lot of work to work really closely with the FDA on the design of this study and with a lot of the thought leaders in the field of Actual health, to really think about what are the endpoints, what is the patient population, How do we categorize them in this exploratory study? So we could come out the other end the way we have, which I couldn't be more thrilled to have come out the other end of it with basically now Having really defined the patient population and the study endpoints that we can take forward into the Phase 3 and have the Phase 2b really be a roadmap for that.

Speaker 1

And I say all of that to say, really in the field of women's health and women's sexual health, Quite frankly, Dare is seen as very much the thought leader in this area. And I will say Every organization who has thought about sexual dysfunction in women and particularly arousal disorder and Sildenafil Cream specifically has certainly looked to Dare as the leader In this area, in the work we've done already with the FDA and in the work that we've done with all of the thought leaders to prepare for this end of Phase 2 meeting and design a Phase 3 program that makes sense. So not to say that Companies may or may not, right, want to have, a say in what that development program looks like. But I think It's really wonderful to be in a position where we're able to say and not in a boasty way, but just state reality. We've done more work in this therapeutic Category than anyone has and we're very much seen as the experts and the leaders.

Speaker 5

Great. That's really helpful. And Sabrina, I guess On Ovaprene, obviously primary endpoint is basically just preventing pregnancy. Are there Any other endpoints in the study that we should be focused on? Thank you.

Speaker 1

Thanks for asking that. We now this is one where we've done we did a lot With Bayer, in the design of the study. And as you know, contraceptive trials, on the one hand, it's very cut and dry. I mean, you're looking at whether or not someone gets pregnant. But because Evaprene is such an innovative disruptive technology, There are a number of things that we and Bayer aligned on that we would also be collecting in this study in terms of just the her experience With the product, so questions really around things that are captured on Electron Diary around her experience with the product, or use of the product, so that we have those insights.

Speaker 1

And then additionally, because it's Once a month product, again similarly there are aspects of that that we're hoping to collect in the data from the trial again kind of related to that Experience perspective, as well as safety, there are a number of safety endpoints in this study as well to really Demonstrate kind of the convenience and safety of using a product of this nature. So when we ultimately do report the findings, It will be very much as I alluded to in my comments. Absolutely, it's about efficacy, but we have also worked very closely with Bayer to make Sure. In this study that we're collecting a lot of really useful, right, and to John's point about commercialization, Useful data around usability and the patients and sort of her experience with the product.

Speaker 5

Okay, great. Thank you so much. Yes.

Operator

We have no further questions at this time. I'll turn it back to Ms. Johnson for any closing remarks.

Speaker 1

Great. Well, thank you. Thanks everyone for taking the time this afternoon. I know it's a busy time of year, earnings season. So I appreciate you dialing in to hear about our recent updates and our ongoing commitment to drive value for all of Dare's stakeholders by addressing unmet needs in women's health.

Speaker 1

And as you heard today, we are prioritizing women's health and well-being by working to expand treatment options where none exist or improve the current standard of care to address persistent unmet needs. We're working closely with our collaborators, Including the leading players we talked about today in women's health, Organon and Bayer, to bring these treatments to women around the world who need them. And ultimately, we believe we are uniquely positioned to improve quality of life for millions of women of Willman. We look forward to keeping you updated on our progress toward the milestones we discuss today. Thank you so much.

Operator

Ladies and gentlemen, this concludes today's conference call. Thank you for participating. You may now disconnect.

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Key Takeaways

  • In Q3, Dare achieved its first commercial milestone for Zaciato, reported positive Phase 2b data for Sildenafil Cream, and made progress toward patient enrollment in the pivotal Phase 3 study of Ovaprene.
  • Additional Phase 2b RESPOND data for Sildenafil Cream support using the same co-primary endpoints and a broader FSIAD population in Phase 3, positioning it as the potential first FDA-approved treatment for female sexual arousal disorders.
  • Ovaprene remains on track to start its pivotal Phase 3 trial in Q4 2023 with NICHD/CCTN support as a single‐arm study for a first-in-category hormone-free monthly intravaginal contraceptive targeting roughly 35 million U.S. women.
  • Under the Organon partnership, initial U.S. shipments of Zaciato have begun, triggering a $1.8 million Q4 milestone and paving the way for tiered royalties plus up to $180 million in future milestones.
  • For Q3, Dare reported $2.7 million in G&A and $6.7 million in R&D expenses, recognized $1 million in license revenue, incurred an $8.3 million loss, and ended the quarter with $13.9 million in cash while pursuing creative, non-dilutive funding strategies.
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Earnings Conference Call
Daré Bioscience Q3 2023
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