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VYNE Therapeutics Reports 2024 Fourth Quarter and Year-End Financial Results and Provides Business Update

1. VYNE expects Phase 2b vitiligo results in mid-2025. 2. Phase 1b psoriasis trial for VYN202 initiated, results due 2025. 3. VYNE's cash runway extends into the second half of 2026. 4. 2024 R&D expenses surged to $30.9 million, increasing focus on repibresib. 5. Q4 2024 net loss is $12 million, with ongoing funding concerns.

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$2.3903/06 08:06 AM EDTEvent Start
$2.2503/07 02:40 PM EDTLatest Updated
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Why Bullish?

Upcoming clinical trial results could drive VYNE's stock performance positively, as seen with other biotech firms. Historical instances show stock price increases following successful trial report announcements.

How important is it?

The article outlines significant clinical milestones and financial health that impact investor sentiment and market perception. Clinical outcomes can significantly affect stock dynamics, elevating VYNE's attractiveness to investors.

Why Short Term?

Immediate effects expected due to upcoming data readouts in mid-2025 and year-end 2025. Rapid market responses to clinical data announcements affect short-term stock movement.

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March 06, 2025 08:00 ET  | Source: VYNE Therapeutics Inc. Repibresib gel (VYN201) Phase 2b vitiligo top-line results expected in mid-2025VYN202 Phase 1b psoriasis trial initiated with results anticipated by year-end 2025Expected cash runway into 2H 2026 BRIDGEWATER, N.J., March 06, 2025 (GLOBE NEWSWIRE) -- VYNE Therapeutics Inc. (Nasdaq: VYNE) (“VYNE” or the “Company”), a clinical-stage biopharmaceutical company focused on developing differentiated therapies to treat chronic inflammatory and immune-mediated conditions with high unmet need, today announced financial results as of and for the fourth quarter and year ended December 31, 2024, and provided a business update. “Based on our significant progress in 2024, we are now positioned to announce two key data readouts for repibresib gel and VYN202 in 2025,” said David Domzalski, President and Chief Executive Officer of VYNE. “We are off to a strong start in 2025. In January, we announced the completion of enrollment in the Phase 2b trial of our locally administered pan-BD BET inhibitor, repibresib, in nonsegmental vitiligo, and we expect to report topline results in mid-2025. We also recently initiated the Phase 1b trial of our oral BD2-selective BET inhibitor, VYN202, in subjects with moderate-to-severe plaque psoriasis, and we anticipate reporting topline results from this trial by the end of this year.” Recent Pipeline Updates Repibresib gel (VYN201), a locally-administered small molecule pan-BD BET inhibitor (Phase 2b, nonsegmental vitiligo): Top-line results from the Phase 2b trial are expected in mid-2025. The fully enrolled, Phase 2b trial (NCT06493578) is a randomized, double-blind, vehicle-controlled trial evaluating the efficacy, safety and pharmacokinetics of once-daily repibresib gel in three dose cohorts (1%, 2% or 3% concentrations) compared to vehicle for 24 weeks in subjects with active or stable nonsegmental vitiligo. Subjects have been randomized equally (1:1:1:1 ratio) across the active drug cohorts or vehicle (approximately 45 subjects in each arm). Top-line results from the 24-week double-blind, vehicle-controlled portion of the trial are expected mid-year.Following the 24-week treatment period, subjects who have been randomized in the three active dose cohorts will continue treatment with their respective dose concentrations for an additional 28-week active treatment extension. Subjects who have been randomized in the vehicle group during the initial 24-week treatment period will be equally re-randomized into one of the three active dose cohorts for an additional 28 weeks. VYN202, an oral small molecule BD2-selective inhibitor: Top-line results from the Phase 1b trial are expected by year-end 2025. In February 2025, the Company announced the initiation of patient enrollment in the Phase 1b trial which is a randomized, double-blind, placebo-controlled trial evaluating the safety, tolerability and pharmacokinetics of once-daily VYN202 in three dosing cohorts (0.25 mg, 0.5 mg, 1 mg doses) compared to placebo, for 12 weeks in subjects with moderate-to-severe plaque psoriasis. Exploratory efficacy of VYN202 will also be evaluated, including measures of psoriasis area and severity index, Static Physician Global Assessment, scalp disease, quality of life, and biomarker analyses. Subjects will be randomized equally (1:1:1:1, approximately 20 subjects per arm) across the active drug cohorts or placebo. Following the 12-week treatment period, all subjects will be followed for a 4-week safety period. Upcoming Conference Participation Investor Conferences. VYNE will be participating in the upcoming Leerink Partners Global Healthcare Conference, taking place in Miami from March 10-12, 2025, as well as the H.C. Wainwright 3rd Annual Autoimmune & Inflammatory Disease Virtual Conference being held on March 27, 2025. Financial Results as of and for the Year Ended December 31, 2024 Cash position. As of December 31, 2024, VYNE had $61.5 million of cash, cash equivalents and marketable securities. Based on current operating assumptions, VYNE believes its cash, cash equivalents and marketable securities as of December 31, 2024 will be sufficient to fund its operations into the second half of 2026. Share count. As of December 31, 2024, VYNE had 14,830,013 common shares issued and outstanding, and outstanding pre-funded warrants to purchase 27,842,740 shares of common stock at an exercise price of $0.0001 per share. Revenues. Revenues totaled $0.5 million and $0.4 million for the years ended December 31, 2024 and 2023, respectively, consisting of royalty revenue from the Company's royalty agreement with LEO Pharma A/S, to whom VYNE previously licensed the rights to Finacea® foam. Research and development expenses. VYNE’s research and development expenses for the years ended December 31, 2024 and 2023 were $30.9 million and $16.3 million, respectively. The increase was primarily due to an increase of $11.7 million in expenses for repibresib, an increase of $2.5 million in expenses for VYN202 and an increase of $0.8 million of employee-related expenses following the hiring of additional research and development personnel. The $11.7 million increase in expenses for repibresib primarily relates to preparatory activity and clinical trial costs incurred for VYNE's ongoing Phase 2b trial of repibresib in subjects with nonsegmental vitiligo. The $2.5 million increase in expenses for VYN202 is primarily associated with costs incurred for our Phase 1a SAD/MAD trial which was completed in the fourth quarter of 2024. Both trials were initiated in June 2024. These increases were partially offset by lower consulting expenses of $0.4 million. General and administrative expenses. VYNE’s general and administrative expenses for the years ended December 31, 2024 and 2023 were approximately $13.2 million and $13.4 million, respectively. The decrease was primarily driven by a reduction in employee related expenses of $0.9 million, partially offset by increased consulting and professional fees of $0.8 million. Net loss. Net loss and net loss per share for the year ended December 31, 2024 was $39.8 million and $0.93, respectively, compared to a net loss and net loss per share of $28.5 million and $2.78, for the comparable period in 2023. About VYNE Therapeutics Inc. VYNE is a clinical-stage biopharmaceutical company focused on developing differentiated therapies to treat chronic inflammatory and immune-mediated conditions with high unmet need. VYNE's unique and proprietary BET inhibitors, which comprise its InhiBET™ platform, are designed to overcome limitations of early generation BET inhibitors by leveraging alternative routes of administration and enhanced selectivity. For more information about VYNE Therapeutics Inc. or its product candidates, visit www.vynetherapeutics.com. VYNE may use its website to comply with its disclosure obligations under Regulation FD. Therefore, investors should monitor VYNE’s website in addition to following its press releases, filings with the U.S. Securities and Exchange Commission, public conference calls, and webcasts. Investor Relations:John FrauncesLifeSci Advisors, LLC917-355-2395jfraunces@lifesciadvisors.com Tyler ZerondaVYNE Therapeutics Inc.908-458-9106Tyler.Zeronda@VYNEtx.com Media Relations: Mike BeyerSam Brown Inc.312-961-2502mikebeyer@sambrown.com Cautionary Statement Regarding Forward-Looking Statements This release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including, but not limited to, statements regarding the clinical development of, and timing for reporting top-line results from trials of, repibresib and VYN202, the impact of the reported top-line results from trials on clinical development, VYNE's participation in upcoming conferences, VYNE’s projected cash runway, and other statements regarding the future expectations, plans and prospects of VYNE. All statements in this press release which are not historical facts are forward-looking statements. Any forward-looking statements are based on VYNE’s current knowledge and its present beliefs and expectations regarding possible future events and are subject to risks, uncertainties and assumptions that could cause actual results to differ materially and adversely from those set forth or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to: VYNE’s ability to successfully develop its product candidates; the timing of commencement of future preclinical studies and clinical trials; VYNE’s ability to complete and receive favorable results from clinical trials of its product candidates; VYNE’s ability to obtain additional funding, either through equity or debt financing transactions or collaboration arrangements; and VYNE’s ability to comply with various regulations applicable to its business. For a discussion of other risks and uncertainties, and other important factors, any of which could cause VYNE’s actual results to differ from those contained in the forward-looking statements, see the section titled “Risk Factors” in VYNE’s Annual Report on Form 10-K for the year ended December 31, 2024, and VYNE’s other filings from time to time with the U.S. Securities and Exchange Commission. Although VYNE believes these forward-looking statements are reasonable, they speak only as of the date of this announcement and VYNE undertakes no obligation to update publicly such forward-looking statements to reflect subsequent events or circumstances, except as otherwise required by law. Given these risks and uncertainties, you should not rely upon forward-looking statements as predictions of future events. Third-party products and company names mentioned herein may be the trademarks of their respective owners.  VYNE THERAPEUTICS INC.CONSOLIDATED BALANCE SHEETS(U.S. dollars in thousands, except share and per share data)(Unaudited)   December 31   2024   2023 Assets    Current Assets:    Cash and cash equivalents $19,926  $30,620 Restricted cash  —   54 Investment in marketable securities  41,590   62,633 Prepaid and other current assets  2,921   2,656 Total Current Assets  64,437   95,963 Non-current Assets:    Property and equipment, net  113   — Operating lease right of use assets  93   207 Non-current prepaid expenses and other assets  2,262   1,515 Total Non-current Assets  2,468   1,722 Total Assets $66,905  $97,685      Liabilities and Shareholders’ Equity    Current Liabilities:    Trade payables $2,707  $1,659 Accrued expenses  9,272   4,119 Employee-related obligations  1,428   1,645 Operating lease liabilities  99   115 Other current liabilities  1,313   — Total Current Liabilities  14,819   7,538 Long-term Liabilities:    Non-current operating lease liabilities  —   99 Other liabilities  —   1,313 Total Long-term Liabilities  —   1,412 Total Liabilities  14,819   8,950      Commitments and Contingencies         Shareholders' Equity:    Preferred stock: $0.0001 par value; 20,000,000 shares authorized at December 31, 2024 and 2023; no shares issued and outstanding at December 31, 2024 and 2023  —   — Common stock: $0.0001 par value; 150,000,000 shares authorized at December 31, 2024 and December 31, 2023; 14,830,013 and 14,098,888 shares issued and outstanding at December 31, 2024 and 2023, respectively  1   1 Additional paid-in capital  783,235   780,044 Accumulated other comprehensive income  20   26 Accumulated deficit  (731,170)  (691,336)Total Shareholders' Equity  52,086   88,735 Total Liabilities and Shareholders’ Equity $66,905  $97,685   VYNE THERAPEUTICS INC.CONSOLIDATED STATEMENTS OF OPERATIONS(U.S. dollars in thousands, except per share data)(Unaudited)   Three Months EndedDecember 31, Year Ended December 31,   2024   2023   2024   2023 Revenues        Royalty revenues $84  $76  $501  $424 Total revenues  84   76   501   424          Operating expenses        Research and development  9,684   3,023   30,946   16,307 General and administrative  3,170   3,885   13,192   13,375 Total operating expenses  12,854   6,908   44,138   29,682 Operating loss  (12,770)  (6,832)  (43,637)  (29,258)Other income, net  760   680   3,834   1,386 Loss from continuing operations before income taxes  (12,010)  (6,152)  (39,803)  (27,872)Income tax expense  4   —   4   — Loss from continuing operations  (12,014) $(6,152)  (39,807)  (27,872)Loss from discontinued operations, net of income taxes  (8)  (36)  (27)  (580)Net loss $(12,022) $(6,188) $(39,834) $(28,452)         Loss per share from continuing operations, basic and diluted $(0.28) $(0.20) $(0.93) $(2.72)Loss per share from discontinued operations, basic and diluted $0.00  $0.00  $0.00  $(0.06)Loss per share, basic and diluted $(0.28) $(0.20) $(0.93) $(2.78)         Weighted average shares outstanding - basic and diluted  42,597   31,050   42,589   10,273 

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