Full Press Release Details
VYNE Reports 2023 Fourth Quarter and Year-End
Financial Results and Provides Business Update
| 2023 was a transformative year for VYNE, marked by the achievement of clinical proof-of-concept for VYN201 in vitiligo and a successful financing with a syndicate of leading institutional investors | ||
| Anticipate commencing a Phase 2b trial for VYN201 and a Phase 1a trial for VYN202 in Q2 2024 | ||
| Ended 2023 with $93.3 million of cash, cash equivalents, restricted cash and marketable securities, providing runway through the end of 2025 and multiple expected clinical milestones |
BRIDGEWATER, N.J., February 29, 2024 -- VYNE
Therapeutics Inc. (Nasdaq: VYNE) ("VYNE" or the "Company"), a clinical-stage biopharmaceutical company focused
on developing proprietary, innovative and differentiated therapies for the treatment of immuno-inflammatory conditions, today announced
financial results for the fourth quarter and year ended December 31, 2023 and provided a business update.
"We have entered 2024 with positive momentum, following an exciting
year highlighted by our clinical proof-of-concept data for VYN201 and a successful financing with leading healthcare institutional investors,"
said David Domzalski, President and CEO of VYNE. "We have made excellent progress with our VYN201 program and remain on track to
initiate a Phase 2b trial in nonsegmental vitiligo next quarter. In addition, we expect to submit supplemental nonclinical information
to the FDA in the coming weeks in support of our IND for VYN202, and assuming clearance by the FDA, we expect to commence our Phase 1a
SAD/MAD trial next quarter as well. We look forward to providing updates on our programs over the coming months."
Recent Pipeline Updates
VYN201, a locally-administered pan-BD BET inhibitor:
| Selected formulation for Phase 2b trial - Following extensive testing, VYNE plans to evaluate VYN201 in a once-daily gel formulation for the upcoming Phase 2b trial in patients with nonsegmental vitiligo. The Company believes the gel formulation may provide additional clinical benefits based on improved dermal penetration properties compared to the ointment that was evaluated in the Phase 1b trial. | ||
| Engaged experienced contract research organization ("CRO") - VYNE has engaged a CRO with extensive experience conducting Phase 2 and Phase 3 vitiligo trials for its upcoming Phase 2b trial. Trial startup activities are ongoing with patient enrollment expected to begin in the second quarter of 2024. Top line results from the 24-week double-blind portion of the Phase 2b trial are anticipated in mid-2025. | ||
| Submitted Phase 2b trial design to FDA - The Phase 2b trial is anticipated to be a 24-week randomized, double-blind, vehicle-controlled trial with a separate active treatment extension phase to 52 weeks. Pending the U.S. Food and Drug Administration's ("FDA") acceptance of the protocol, the trial will evaluate three or four arms (including vehicle) of once-daily treatment with VYN201 gel, with each arm enrolling between 40 and 50 patients with active or stable nonsegmental vitiligo. The primary efficacy endpoint of the trial will be an evaluation of the proportion of subjects achieving FVASI50 at week 24 compared to vehicle. | ||
| Announced positive biomarker data from Phase 1b trial - Earlier this year, VYNE announced that exploratory data for the 1.0% and 2.0% cohorts from the Phase 1b trial showed that VYN201 treatment demonstrated biological activity and a positive effect on certain key biomarkers relevant to vitiligo disease severity and progression. This data supports VYN201's rapid onset of action and previously announced positive clinical results. |
VYN202, an oral small molecule BD2-selective BET inhibitor:
| Phase 1a trial expected to start in Q2 - Assuming the IND is cleared by the FDA, VYNE expects to initiate its Phase 1a single ascending dose/multiple ascending dose (SAD/MAD) trial in healthy volunteers in the second quarter of 2024, with top line results from the trial anticipated in the second half of 2024. If the Phase 1a portion of the trial is successfully completed, VYNE plans to initiate Phase 1b trials in subjects with moderate-to-severe plaque psoriasis and moderate-to-severe adult-onset rheumatoid arthritis, with top line results anticipated in the second half of 2025. | ||
| Trial startup activities substantially complete - VYNE has engaged a CRO for its Phase 1a trial and has completed the manufacturing of VYN202 capsules. |
Upcoming Congress and Conference Participation
| Global Vitiligo Foundation Annual Scientific Symposium - Dr. Iain Stuart, Chief Scientific Officer of VYNE, will present data from the Phase 1b trial for VYN201 in nonsegmental vitiligo at the Foundation's annual symposium held on March 7, 2024 in San Diego. | ||
| Investor Conferences - VYNE will be participating in the upcoming TD Cowen 44th Annual Health Care Conference, taking place in Boston on March 4-6, 2024, as well as the H.C. Wainwright 2nd Annual Autoimmune and Inflammatory Disease Conference being held virtually on March 28, 2024. |
| Financial Performance | Three months ended December 31, | Year ended December 31, | ||||||||||||||
| (in thousands) | 2023 | 2022 | 2023 | 2022 | ||||||||||||
| Loss from continuing operations (GAAP) | $ | (6,152 | ) | $ | (7,761 | ) | $ | (27,872 | ) | $ | (33,945 | ) | ||||
| Adjusted loss from continuing operations (non-GAAP)* | $ | (5,442 | ) | $ | (6,694 | ) | $ | (24,567 | ) | $ | (29,296 | ) | ||||
| Net loss (GAAP) | $ | (6,188 | ) | $ | (9,945 | ) | $ | (28,452 | ) | $ | (23,210 | ) | ||||
| Adjusted net loss (non-GAAP)* | $ | (5,478 | ) | $ | (8,878 | ) | $ | (25,147 | ) | $ | (18,913 | ) |
*See "Non-GAAP Financial Measures" elsewhere in this earnings
Liquidity and Capital Resources
As of December 31, 2023, VYNE had cash, cash
equivalents, restricted cash and marketable securities of $93.3 million. VYNE believes its cash, cash equivalents, restricted cash and
marketable securities as of December 31, 2023 will be sufficient to fund its operations through the end of 2025. See Note 1 to VYNE's
audited consolidated financial statements included in VYNE's Annual Report on Form 10-K for additional discussion on liquidity
and capital resources.
Financial Results for the Year Ended December 31, 2023
Revenues for the year ended December 31, 2023 totaled $0.4 million compared to $0.5 million for the year ended December 31,
2022, consisting of royalty revenue from sales of Finacea foam by LEO Pharma, to whom VYNE previously licensed the rights to that product.
and development expenses. VYNE's research and development expenses for the year ended December 31, 2023 were
$16.3 million, representing a decrease of $2.1 million, or 11.3%, as compared to $18.4 million for the year ended December 31, 2022.
The decrease was primarily due to lower employee-related expenses of $3.8 million and decreased spending for FMX114 and VYN201 of
$2.7 million and $2.2 million, respectively. The decrease was partially offset by increased
expenses for VYN202 of $6.7 million, including $4.0 million paid in connection with entering into a license agreement with Tay Therapeutics
and administrative expenses. VYNE's general and administrative expenses for the year ended December 31, 2023
were $13.4 million, representing a decrease of $3.0 million, or 18.4%, compared to $16.4 million for the year ended December 31,
2022. The decrease was primarily driven by lower rent and corporate insurance costs of $1.6 million
and decreased consulting and professional fees of $1.1 million.
loss. Net loss and net loss per share for the year ended December 31, 2023 was $28.5 million and $2.78, respectively,
compared to a net loss and net loss per share of $23.2 million and $7.28 for the comparable period in 2022, respectively. Net loss for
2023 included a $0.6 million loss from discontinued operations, net of income taxes, and net loss for 2022 included income of $10.7 million
from discontinued operations, net of income taxes.
About VYNE Therapeutics Inc.
VYNE's mission is to improve the lives of
patients by developing proprietary, innovative and differentiated therapies for the treatment of immuno-inflammatory conditions. The Company's
unique and proprietary bromodomain & extra-terminal (BET) domain inhibitors, which comprise its InhiBET platform, include
a locally administered pan-BD BET inhibitor (VYN201) and an orally available BD2-selective BET inhibitor (VYN202) that were licensed from
Tay Therapeutics Limited.
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.
LifeSci Advisors, LLC
VYNE Therapeutics Inc.
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
VYNE's plans, regulatory approvals, development timelines for VYN201 and VYN202, VYNE's InhiBET platform,
VYNE's projected cash runway through the end of 2025, 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 the commencement of future non-clinical studies
and clinical trials; VYNE's ability to enroll patients and successfully progress, complete, and receive favorable results in clinical
trials for its product candidates; VYNE's ability to comply with various regulations applicable to its business; VYNE's ability
to create intellectual property and the scope of protection it is able to establish and maintain for intellectual property rights covering
its product candidates, including the projected terms of patent protection; risks that any of VYNE's patents may be held to be narrowed,
invalid or unenforceable or one or more of VYNE's patent applications may not be granted and potential competitors may also seek
to design around VYNE's granted patents or patent applications; estimates of VYNE's expenses, capital requirements, its needs
for additional financing and its ability to obtain additional capital on acceptable terms or at all; VYNE's expectations regarding
licensing, business transactions and strategic operations; VYNE's future financial performance and liquidity; and potential volatility
in VYNE's stock price that may result in rapid and substantial increases or decreases in the stock price that may or may not be
related to VYNE's operating performance or prospects. 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, 2023, as well as discussions
of potential risks, uncertainties, and other important factors in VYNE's subsequent filings 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
VYNE THERAPEUTICS INC.
CONSOLIDATED BALANCE SHEETS
(U.S. dollars in thousands, except share and per
| December 31, | ||||||||
| 2023 | 2022 | |||||||
| Assets | ||||||||
| Current Assets: | ||||||||
| Cash and cash equivalents | $ | 30,620 | $ | 30,908 | ||||
| Restricted cash | 54 | 67 | ||||||
| Investment in marketable securities | 62,633 | - | ||||||
| Amount due from sale of MST Franchise | - | 5,000 | ||||||
| Prepaid and other current assets | 2,656 | 2,300 | ||||||
| Total Current Assets | 95,963 | 38,275 | ||||||
| Non-current Assets: | ||||||||
| Operating lease right-of-use assets | 207 | - | ||||||
| Non-current prepaid expenses and other assets | 1,515 | 2,483 | ||||||
| Total Non-current Assets | 1,722 | 2,483 | ||||||
| Total Assets | $ | 97,685 | $ | 40,758 | ||||
| Liabilities, Mezzanine Equity and Shareholders' Equity | ||||||||
| Current Liabilities: | ||||||||
| Trade payables | $ | 1,659 | $ | 2,386 | ||||
| Accrued expenses | 4,119 | 4,381 | ||||||
| Employee-related obligations | 1,645 | 2,372 | ||||||
| Liability for employee severance benefits | - | 206 | ||||||
| Operating lease liabilities | 115 | - | ||||||
| Total Current Liabilities | 7,538 | 9,345 | ||||||
| Long-term Liabilities: | ||||||||
| Non-current operating lease liabilities | 99 | - | ||||||
| Other liabilities | 1,313 | - | ||||||
| Total Long-term Liabilities | 1,412 | - | ||||||
| Total Liabilities | 8,950 | 9,345 | ||||||
| Commitments and Contingencies | ||||||||
| Mezzanine Equity: | ||||||||
| Convertible Preferred Stock: $0.0001 par value; 20,000,000 shares authorized at December 31, 2023 and December 31, 2022; Series A Preferred Stock: 0 and 3,000 shares issued and outstanding at December 31, 2023 and December 31, 2022, respectively | - | 211 | ||||||
| Shareholders' Equity: | ||||||||
| Preferred stock: $0.0001 par value; 20,000,000 shares authorized at December 31, 2023 and December 31, 2022, respectively; no shares issued and outstanding at December 31, 2023 and December 31, 2022, respectively | - | - | ||||||
| Common stock: $0.0001 par value; 150,000,000 shares authorized at December 31, 2023 and December 31, 2022; 14,098,888 and 3,229,704 shares issued and outstanding at December 31, 2023 and December 31, 2022, respectively | 1 | - | ||||||
| Additional paid-in capital | 780,044 | 693,937 | ||||||
| Accumulated other comprehensive income | 26 | - | ||||||
| Accumulated deficit | (691,336 | ) | (662,735 | ) | ||||
| Total Shareholders' Equity | 88,735 | 31,202 | ||||||
| Total Liabilities, Mezzanine Equity and Shareholders' Equity | $ | 97,685 | $ | 40,758 |
VYNE THERAPEUTICS INC.
CONSOLIDATED STATEMENTS OF OPERATIONS
(U.S. dollars in thousands, except per share data)
| Three Months Ended December 31, | Year ended December 31, | |||||||||||||||
| 2023 | 2022 | 2023 | 2022 | |||||||||||||
| Revenues | ||||||||||||||||
| Royalty revenues | $ | 76 | $ | 6 | $ | 424 | $ | 477 | ||||||||
| Total Revenues | 76 | 6 | 424 | 477 | ||||||||||||
| Operating Expenses: | ||||||||||||||||
| Research and development | 3,023 | 4,279 | 16,307 | 18,385 | ||||||||||||
| General and administrative | 3,885 | 3,711 | 13,375 | 16,387 | ||||||||||||
| Total Operating Expenses | 6,908 | 7,990 | 29,682 | 34,772 | ||||||||||||
| Operating Loss | (6,832 | ) | (7,984 | ) | (29,258 | ) | (34,295 | ) | ||||||||
| Other income, net | 680 | 236 | 1,386 | 363 | ||||||||||||
| Loss from continuing operations before income taxes | (6,152 | ) | (7,748 | ) | (27,872 | ) | (33,932 | ) | ||||||||
| Income tax expense | - | 13 | - | 13 | ||||||||||||
| Loss from continuing operations | (6,152 | ) | $ | (7,761 | ) | (27,872 | ) | (33,945 | ) | |||||||
| (Loss) income from discontinued operations, net of income taxes | (36 | ) | (2,184 | ) | (580 | ) | 10,735 | |||||||||
| Net Loss | $ | (6,188 | ) | $ | (9,945 | ) | $ | (28,452 | ) | $ | (23,210 | ) | ||||
| Loss per share from continuing operations, basic and diluted | $ | (0.20 | ) | $ | (2.60 | ) | $ | (2.72 | ) | $ | (10.65 | ) | ||||
| (Loss) income per share from discontinued operations, basic and diluted | $ | - | $ | (0.73 | ) | $ | (0.06 | ) | $ | 3.37 | ||||||
| Loss per share, basic and diluted | $ | (0.20 | ) | $ | (3.33 | ) | $ | (2.78 | ) | $ | (7.28 | ) | ||||
| Weighted average shares outstanding - basic and diluted | 31,050 | 2,985 | 10,273 | 3,186 |
Non-GAAP Financial Measures
In evaluating the operating performance of its business, VYNE's
management considers adjusted net loss, adjusted net loss per share, adjusted loss from continuing operations, adjusted total operating
expenses (including adjusted research and development expense and adjusted general and administrative expense), adjusted operating loss
and adjusted loss per share from continuing operations. These non-GAAP financial measures exclude stock-based
compensation charges that are required by GAAP. The Company believes that these non-GAAP financial measures provide management,
analysts, investors and other users of the Company's financial information with meaningful supplemental information regarding the
performance of the Company's business by excluding the effect of certain non-cash expenses and items that VYNE believes may not