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Sol-Gel Reports First Quarter 2026 Financial Results and Provides Corporate Updates

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Sol-Gel (NASDAQ: SLGL) reported Q1 2026 revenue of $0.1 million, down from $1.0 million in Q1 2025, and a net loss of $3.7 million ($1.31 per share), versus a $8.8 million loss a year earlier.

Research and development expenses fell to $2.8 million from $8.8 million. Cash, deposits and marketable securities totaled $52.8 million as of March 31, 2026, which is expected to fund operations into Q1 2028.

Recent milestones include a Notice of Allowance for a method-of-use patent protecting SGT-610 until 2044, an oversubscribed $33.1 million underwritten offering, ongoing Phase 3 development of SGT-610 in Gorlin syndrome with top-line results anticipated in Q4 2026, and an exclusive TWYNEO® commercialization license in India with Sun Pharma plus broader global partnership expansion.

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AI-generated analysis. Not financial advice.

Positive

  • Notice of Allowance extends SGT-610 method-of-use patent protection in the U.S. until 2044
  • Oversubscribed underwritten offering raised approximately $33.1 million in gross proceeds
  • Total cash, deposits and marketable securities of $52.8 million at March 31, 2026
  • Company expects cash resources to fund requirements into the first quarter of 2028
  • R&D expenses decreased to $2.8 million from $8.8 million year-over-year
  • Net loss narrowed to $3.7 million from $8.8 million year-over-year
  • Global TWYNEO/EPSOLAY deals may provide up to $4.5 million in milestones
  • Royalty revenue from TWYNEO/EPSOLAY partners is anticipated to potentially reach about $10 million annually by 2031

Negative

  • Q1 2026 revenue declined to $0.1 million from $1.0 million year-over-year
  • Company reported a Q1 2026 net loss of $3.7 million
  • TWYNEO and EPSOLAY partner launches are expected mainly in 2028 and 2027, delaying potential royalty ramp

Key Figures

Underwritten offering proceeds: $33.1 million Q1 2026 revenue: $0.1 million R&D expenses: $2.8 million +5 more
8 metrics
Underwritten offering proceeds $33.1 million Oversubscribed offering closed March 2026
Q1 2026 revenue $0.1 million Quarter ended March 31, 2026 vs. $1.0M in Q1 2025
R&D expenses $2.8 million Q1 2026 vs. $8.8M in Q1 2025
Net loss $3.7 million ($1.31/share) Q1 2026 vs. $8.8M ($3.2/share) in Q1 2025
Cash and equivalents $10.1 million As of March 31, 2026 (excludes $42.7M marketable securities)
Marketable securities $42.7 million As of March 31, 2026; total liquidity $52.8M
Potential milestones $4.5 million Upfront and regulatory milestones from ex-U.S. TWYNEO/EPSOLAY deals
Potential annual royalties $10 million Projected TWYNEO/EPSOLAY royalties by 2031 post-launch

Market Reality Check

Price: $73.80 Vol: Volume 28,643 is in line ...
normal vol
$73.80 Last Close
Volume Volume 28,643 is in line with the 20-day average of 25,924 (relative volume 1.1x) normal
Technical Trading above 200-day MA of 52.87 with pre-news price at 73.8

Peers on Argus

SLGL was down 0.94% pre-news while biotech peers were mixed; one close peer, INK...
1 Up

SLGL was down 0.94% pre-news while biotech peers were mixed; one close peer, INKT, appeared on the momentum scanner with a ~5.6% upside move and no news, suggesting today’s setup looked more stock-specific than sector-driven.

Previous Earnings Reports

5 past events · Latest: Nov 20 (Neutral)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Nov 20 Q3 2025 earnings Neutral -0.8% Reported Q3 2025 results with lower revenue, ongoing SGT-610 progress and cash runway.
Aug 15 Q2 2025 earnings Positive +1.3% Q2 2025 beat with $17.2M revenue from Mayne Pharma deal and net income reported.
May 23 Q1 2025 earnings Negative -1.2% Q1 2025 showed higher R&D spend and wider net loss despite revenue doubling to $1M.
Nov 15 Q3 2024 earnings Positive +3.0% Q3 2024 revenue rose to $5.4M with near break-even loss and new license deals.
Aug 16 Q2 2024 earnings Positive +2.6% Q2 2024 delivered $5.4M revenue, net income and extended cash runway into Q1 2026.
Pattern Detected

Earnings-related headlines for Sol-Gel have generally produced modest, directionally consistent moves, with an average absolute move of about 0.95%. Positive or improving fundamentals (revenue spikes, cash runway extensions, licensing deals) have usually coincided with mild gains, while weaker revenue or higher losses have seen small declines, indicating measured, not explosive, reactions to financial updates.

Recent Company History

Recent earnings updates show Sol-Gel using licensing and product sale agreements to generate non-dilutive cash, while advancing SGT-610 through Phase 3. Prior quarters featured swings in revenue, from $0.4M to $17.2M, and periods of both net income and net loss, alongside repeated cash runway extensions into Q1 2026–Q1 2027. Those reports also emphasized global TWYNEO/EPSOLAY deals and steady progress in SGT-610, setting the backdrop for today’s Q1 2026 results, new patent protection, financing, and expanded licensing.

Historical Comparison

+0.9% avg move · This earnings release follows 5 prior earnings updates, which historically moved SLGL about 0.95% on...
earnings
+0.9%
Average Historical Move earnings

This earnings release follows 5 prior earnings updates, which historically moved SLGL about 0.95% on average and tended to track the tone of revenue, cash runway and partnership progress.

Across recent earnings, Sol-Gel has repeatedly extended its cash runway while advancing SGT-610 Phase 3 and expanding TWYNEO/EPSOLAY licensing. The current quarter adds larger cash resources, new IP protection for SGT-610 and broader geographic reach for TWYNEO.

Market Pulse Summary

This announcement combines Q1 2026 results with several strategic milestones: a method-of-use patent...
Analysis

This announcement combines Q1 2026 results with several strategic milestones: a method-of-use patent that protects SGT-610 until 2044, an oversubscribed $33.1M offering, and expanded TWYNEO licensing into India. Revenue declined to $0.1M, but R&D spend and net loss narrowed and cash plus securities reached $52.8M, guiding runway into Q1 2028. Investors may watch SGT-610 Phase 3 timelines, HF-BCC proof-of-concept plans, and the ramp of ex-U.S. royalty streams toward a potential $10M by 2031.

Key Terms

notice of allowance, phase 3 clinical trial, proof-of-concept study, gorlin syndrome
4 terms
notice of allowance regulatory
"received a Notice of Allowance (U.S. Patent Application No. 19/266,342)"
A notice of allowance is an official confirmation from a patent office that a patent application has met all necessary requirements and is approved for granting. It signals that the invention is likely to receive legal protection soon, which can be important for investors considering the value and exclusivity of a new product or technology. Think of it as a green light indicating that the invention is on track to become legally protected.
phase 3 clinical trial medical
"Pivotal Phase 3 clinical trial of SGT-610 (patidegib gel, 2%) for Gorlin"
A phase 3 clinical trial is a large-scale study that tests a new medical treatment or drug to determine if it is safe and effective for widespread use. It often involves hundreds or thousands of participants and compares the new treatment to existing options or a placebo. For investors, the results of this phase are crucial, as successful outcomes can lead to regulatory approval and commercial success, while failures may halt development.
proof-of-concept study medical
"preparations for a proof-of-concept study of SGT-610 in HF-BCC are ongoing"
A proof-of-concept study is an early-stage test that checks whether a new drug, device, or treatment produces the intended effect in people or in lab models — like a pilot run to see if an idea actually works. For investors, its results are a key early signal: positive findings can greatly reduce uncertainty and boost a project’s value, while negative results often lead to delays, additional costs, or program termination.
gorlin syndrome medical
"Phase 3 clinical trial of SGT-610 (patidegib gel, 2%) for Gorlin syndrome"
A rare inherited genetic condition that increases a person’s lifetime risk of developing multiple skin cancers and other growths, often beginning in childhood or early adulthood. For investors it matters because the small, defined patient group and predictable medical needs make the condition a target for specialized drugs, diagnostics and long‑term care markets; think of it like a known design flaw that creates steady demand for fixes and monitoring.

AI-generated analysis. Not financial advice.

  • Sol-Gel received a Notice of Allowance for a method-of-use patent extending intellectual property protection for topical patidegib (SGT-610) until 2044
  • Sol-Gel completed an oversubscribed underwritten offering, raising gross proceeds of approximately $33.1 million from leading healthcare specialist investors
  • Pivotal Phase 3 clinical trial of SGT-610 (patidegib gel, 2%) for Gorlin syndrome remains ongoing, with top-line results on track for anticipated readout in the fourth quarter of 2026
  • Sol-Gel signed an exclusive license agreement with Sun Pharmaceutical Industries Ltd. for the commercialization of TWYNEO® in India

NESS ZIONA, Israel, May 28, 2026 (GLOBE NEWSWIRE) -- Sol-Gel Technologies, Ltd. (NASDAQ: SLGL), a dermatology company, pioneering treatments for patients with rare and severe skin conditions, today announced financial results for the first quarter ended March 31, 2026, and provided a corporate update.

Q1 2026 and Recent Corporate Developments

  • In May 2026, the company received a Notice of Allowance (U.S. Patent Application No. 19/266,342) from the U.S. Patent and Trademark Office for our patent application covering a method-of-use that is critical to successful topical patidegib therapy. This patent will provide protection for SGT-610 until 2044.
  • In March 2026, Sol-Gel closed an underwritten offering resulting in aggregate gross proceeds of approximately $33.1 million. The offering included participation from new and existing investors, including Great Point Partners, LLC, Trails Edge Capital Partners, Surveyor Capital (a Citadel company), Affinity Asset Advisors, Squadron Capital Management, Stonepine Capital Management and AuGC BioFund. TD Cowen and LifeSci Capital acted as joint book-running managers for the offering.
  • Sol-Gel’s pivotal Phase 3 clinical trial of SGT-610 (patidegib gel, 2%) for Gorlin syndrome continues to advance, and the Company remains on track to report top-line results in the fourth quarter of 2026; preparations for a proof-of-concept study of SGT-610 in HF-BCC are ongoing.
  • In April 2026, Sol-Gel entered into an exclusive license agreement with Sun Pharmaceutical Industries Ltd. for the commercialization of TWYNEO® in India. This agreement is in addition to the eight agreements for the commercialization of TWYNEO® and EPSOLAY Sol-Gel signed during 2024 and 2025 in various territories covering most European countries, South Africa, South Korea, Australia and New Zealand. These already signed agreements, together with agreements we anticipate signing in the future covering Latin American countries, Spain and Portugal, have the potential to provide upfront and regulatory milestone payments of up to $4.5 million. The above excludes Sol-Gel's previously signed agreements with Beimei Pharma (China, Hong Kong, Macau, Taiwan and Israel) and Searchlight Pharma (Canada).
    Based on the forecasts received from Sol-Gel’s current and potential partners, Sol-Gel now expects that TWYNEO and EPSOLAY will launch in the majority of these new territories during 2028 and 2027 respectively, and following launch, these transactions are anticipated to provide Sol-Gel with an annual royalty revenue stream with the potential to reach approximately $10 million by 2031 and potentially grow in subsequent years.

Mr. Mori Arkin, Executive Chairman of Sol-Gel, stated: “The first quarter of 2026 was a period of substantial progress on every front that matters to Sol-Gel. The Notice of Allowance extending the exclusivity of patidegib until 2044 marks a major milestone in the value creation of SGT-610 and Sol-Gel as a company. In parallel, the successful completion of our oversubscribed offering, with broad participation from leading healthcare specialist investors, is expected to provide Sol-Gel with the financial resources to support operations into 2028, allowing us to execute our Phase 3 program of SGT-610 through top-line readout and to support its pre-commercialization activities."

Mr. Arkin further commented: "We believe that the combination of our March 2026 financing and the Notice of Allowance for a method-of-use patent protecting topical patidegib until 2044 fundamentally reshapes the long-term opportunity for SGT-610. We now have both the capital and intellectual property runway to pursue the prevention of new BCCs in Gorlin syndrome, for which top-line results are expected in the fourth quarter of 2026. We continue to be excited about the potential of the high-frequency BCC indication, which could double the commercial potential of patidegib, and we look forward to initiating a proof-of-concept study."

Lastly, Mr. Arkin commented: "The license agreement with Sun Pharma for India, one of the largest dermatology markets in the world, is another important step in unlocking the global value of TWYNEO through partnerships with leading companies in their respective territories. While the commercialization of our legacy products is a non-core business of Sol-Gel, we believe that this activity has the potential to become an asset of substantial value, in the not-too-distant future. At the appropriate time, we plan to monetize this business and use the non-dilutive funds to support our long-term strategy of developing innovative treatments for unmet medical needs in dermatology."

Financial Results for the First Quarter 2026

Revenue for the first quarter was $0.1 million, compared to revenue of $1.0 million for the same period in 2025. The decrease is mainly attributed to a milestone payment from Searchlight in the first quarter of 2025.

Research and development expenses were $2.8 million compared to $8.8 million for the same period in 2025. The decrease of $6.0 million was primarily attributed to a decrease of $3.9 million due to expenses associated with supplier-led manufacturing development to support future commercialization of SGT-610 in the first quarter of 2025, a decrease of $1.1 million in clinical trial expenses related to SGT-610 and a decrease of $0.8 million in expenses related to the manufacturing development of EPSOLAY and TWYNEO.

General and administrative expenses were $1.2 million compared to $1.3 million for the same period in 2025.

Sol-Gel reported a net loss of $3.7 million for the first quarter of 2026 and loss of $1.31 per basic and diluted share, compared to a net loss of $8.8 million and loss of $3.2 per basic and diluted share for the same period in 2025.

As of March 31, 2026, Sol-Gel had $10.1 million in cash, cash equivalents, and deposits and $42.7 million in marketable securities, for a total balance of $52.8 million. The Company expects its cash resources to fund cash requirements into the first quarter of 2028.

About Sol-Gel Technologies

Sol-Gel is a specialized dermatology company advancing innovative therapies for rare and serious skin diseases. Its lead investigational candidate, SGT-610 (patidegib gel, 2%), is a Phase 3, orphan- and breakthrough-designated topical hedgehog inhibitor being developed for the prevention of new basal cell carcinoma (BCC) lesions in patients with Gorlin syndrome, with the potential to offer an improved safety profile relative to oral hedgehog inhibitors. Subject to regulatory approval in Gorlin syndrome, SGT-610 may also represent a future opportunity in high-frequency BCC. Sol-Gel is also advancing SGT-210, an investigational topical EGFR inhibitor for indications with significant unmet need, and has developed two FDA-approved dermatology products, TWYNEO® and EPSOLAY®.

Forward Looking Statements

This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements. including, but not limited to statements regarding the timing of clinical milestones for the Phase 3 program of SGT-610 in Gorlin syndrome, the Company’s cash runway, the timing of the launch of the commercialization of TWYNEO® and EPSOLAY in various territories and the anticipated financial benefits of the Company’s agreements for the commercialization of TWYNEO® and EPSOLAY. In some cases, you can identify forward-looking statements by terminology such as “believe,” “may,” “estimate,” “continue,” “anticipate,” “intend,” “should,” “plan,” “expect,” “predict,” “potential,” or the negative of these terms or other similar expressions. Forward-looking statements are based on information we have when those statements are made or our management’s current expectations and are subject to risks and uncertainties that could cause actual performance or results to differ materially from those expressed in or suggested by the forward-looking statements. Important factors that could cause such differences include, but are not limited to, the risk of a delay in reporting the top-line results of Sol-Gel’s pivotal Phase 3 clinical trial of SGT-610 (patidegib gel, 2%) for Gorlin syndrome, that we will not successfully complete the Gorlin Phase 3 trial or the success of our clinical trials, a delay in the launch of the commercialization of TWYNEO® and EPSOLAY in various territories, that the financial benefits of the Company’s agreements for the commercialization of TWYNEO® and EPSOLAY will not be as anticipated as well as the following factors: (i) the adequacy of our financial and other resources, particularly in light of our history of recurring losses; (ii) our ability to complete the development of our product candidates; (iii) our ability to find suitable co-development partners; (iv) our ability to obtain and maintain regulatory approvals for our product candidates in our target markets, the potential delay in receiving such regulatory approvals and the possibility of adverse regulatory or legal actions relating to our product candidates even if regulatory approval is obtained; (v) our collaborators’ ability to commercialize our pharmaceutical product candidates; (vi) our ability to obtain and maintain adequate protection of our intellectual property; (vii) our collaborators’ ability to manufacture our product candidates in commercial quantities, at an adequate quality or at an acceptable cost; (viii) our collaborators’ ability to establish adequate sales, marketing and distribution channels; (ix) acceptance of our product candidates by healthcare professionals and patients; (x) the possibility that we may face third-party claims of intellectual property infringement; (xi) the timing and results of clinical trials that we may conduct or that our competitors and others may conduct relating to our or their products; (xii) intense competition in our industry, with competitors having substantially greater financial, technological, research and development, regulatory and clinical, manufacturing, marketing and sales, distribution and personnel resources than we do; (xiii) potential product liability claims; (xiv) potential adverse federal, state and local government regulation in the United States, China, Europe or Israel; and (xv) loss or retirement of key executives and research scientists; (xvi) general market, political and economic conditions in the countries in which the Company operates; and, (xvii) the security situation in Israel. These factors and other important factors discussed in the Company's Annual Report on Form 20-F filed with the Securities and Exchange Commission (“SEC”) on March 19, 2026, and our other reports filed with the SEC, could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Except as required by law, we undertake no obligation to update any forward-looking statements in this press release.

 
SOL-GEL TECHNOLOGIES LTD.
CONDENSED CONSOLIDATED BALANCE SHEETS
(U.S. dollars in thousands)
(Unaudited)
    
 December 31, March 31,
 2025 2026
Assets       
CURRENT ASSETS:       
Cash and cash equivalents$11,033  $10,136 
Marketable securities 12,966   42,692 
Accounts receivables 1,968   1,067 
Prepaid expenses and other current assets 1,004   1,894 
TOTAL CURRENT ASSETS 26,971   55,789 
        
NON-CURRENT ASSETS:       
Restricted long-term deposits and cash equivalents 1,324   1,328 
Property and equipment, net 140   136 
Operating lease right-of-use assets 1,027   901 
Other long-term assets 62   - 
Funds in respect of employee rights upon retirement 393   396 
        
TOTAL NON-CURRENT ASSETS 2,946   2,761 
TOTAL ASSETS$29,917  $58,550 
Liabilities and shareholders' equity       
CURRENT LIABILITIES:       
Accounts payable$735  $782 
Other accounts payable 4,941   5,046 
Current maturities of operating leases 495   485 
TOTAL CURRENT LIABILITIES 6,171   6,313 
        
LONG-TERM LIABILITIES:       
Operating leases liabilities 496   377 
Liability for employee rights upon retirement 439   454 
TOTAL LONG-TERM LIABILITIES 935   831 
TOTAL LIABILITIES$7,106  $7,144 
        
SHAREHOLDERS' EQUITY:       
Ordinary shares, NIS 1 par value – authorized: 5,000,000 as of December 31, 2025 and March 31, 2026, respectively; issued and outstanding: 2,786,158 and 3,268,991 as of December 31, 2025 and March 31, 2026, respectively 774   1,321 
Additional paid-in capital 259,047   290,822 
Accumulated deficit (237,010)  (240,737)
TOTAL SHAREHOLDERS' EQUITY 22,811   51,406 
TOTAL LIABILITIES AND SHAREHOLDERS' EQUITY$29,917  $58,550 
        



SOL-GEL TECHNOLOGIES LTD.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(U.S. dollars in thousands)
(Unaudited)
  
 Three months ended
 March 31
 2025
 2026
REVENUES$1,031  $108 
RESEARCH AND DEVELOPMENT EXPENSES 8,843   2,786 
GENERAL AND ADMINISTRATIVE EXPENSES 1,257   1,177 
OPERATING LOSS 9,069   3,855 
FINANCIAL INCOME,net (261)  (128)
LOSS FOR THE PERIOD 8,808   3,727 
        
BASIC AND DILUTED LOSS PER ORDINARY SHARE 3.2   1.31 
WEIGHTED AVERAGE NUMBER OF SHARES OUTSTANDING USED IN COMPUTATION OF BASIC AND DILUTED LOSS PER SHARE * 2,785,762   2,836,907 
      

* The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

Sol-Gel Investor Relations:
Eyal Ben-Or
Chief Financial Officer
ir@sol-gel.com


FAQ

What were Sol-Gel (NASDAQ: SLGL) Q1 2026 financial results?

Sol-Gel reported Q1 2026 revenue of $0.1 million and a net loss of $3.7 million. According to Sol-Gel, research and development expenses were $2.8 million, general and administrative expenses were $1.2 million, and loss per basic and diluted share was $1.31.

How much cash does Sol-Gel (SLGL) have and how long is its runway after Q1 2026?

Sol-Gel held $52.8 million in cash, cash equivalents, deposits and marketable securities as of March 31, 2026. According to Sol-Gel, this liquidity, supported by the $33.1 million March 2026 offering, is expected to fund cash requirements into the first quarter of 2028.

What is the status and timeline of Sol-Gel's SGT-610 Phase 3 trial for Gorlin syndrome?

Sol-Gel’s pivotal Phase 3 trial of SGT-610 (patidegib gel, 2%) for Gorlin syndrome is ongoing. According to Sol-Gel, top-line results remain on track for the fourth quarter of 2026, and preparations continue for a proof-of-concept study in high-frequency basal cell carcinoma.

What new patent protection did Sol-Gel secure for topical patidegib (SGT-610)?

Sol-Gel received a Notice of Allowance for a method-of-use patent covering topical patidegib therapy. According to Sol-Gel, this U.S. patent protection for SGT-610 is expected to extend intellectual property coverage until 2044, supporting its long-term commercial opportunity if development succeeds.

What licensing agreements has Sol-Gel signed for TWYNEO and EPSOLAY and potential revenues?

Sol-Gel signed an exclusive TWYNEO license in India with Sun Pharma plus multiple TWYNEO/EPSOLAY deals across Europe and other regions. According to Sol-Gel, these may provide up to $4.5 million in upfront and milestone payments and royalty revenue potentially reaching about $10 million annually by 2031.

When are TWYNEO and EPSOLAY expected to launch in new territories and impact Sol-Gel (SLGL) royalties?

TWYNEO is now expected to launch in most new territories in 2028 and EPSOLAY in 2027. According to Sol-Gel, following these launches, combined royalty revenue from partners is anticipated to potentially reach approximately $10 million annually by 2031 and may grow thereafter.