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6-K 1 zk2533253.htm 6-K


UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
 
FORM 6-K
 
Report of Foreign Private Issuer
Pursuant to Rule 13a-16 or 15d-16
Under the Securities Exchange Act of 1934
 
For the month of May 2025
 
Commission File Number 001-38367
 
SOL-GEL TECHNOLOGIES LTD.
(Translation of registrant’s name into English)
 
7 Golda Meir Street
Ness Ziona 7403650, Israel
(Address of principal executive offices)

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.
 
Form 20-F ☒           Form 40-F ☐
 
Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1):  ☐

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(7):  ☐





INFORMATION CONTAINED IN THIS REPORT ON FORM 6-K

On May 23, 2025, Sol-Gel Technologies Ltd. (the “Company”) issued a press release entitled “Sol-Gel Reports First Quarter 2025 Results”.

Attached hereto is the following exhibit:

 
This Report is incorporated by reference into the Company’s registration statements on Form S-8 (Registration Nos. 333-223915,  333-270477 and  333-286820), and Form F-3 (Registration No  333-286822), to be a part thereof from the date on which this report is submitted, to the extent not superseded by documents or reports subsequently filed or furnished.






 SIGNATURES
 
Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
 
 
SOL-GEL TECHNOLOGIES LTD.
 
 
 
Date: May 23, 2025
By:
/s/ Eyal Ben-Or
 
 
Eyal Ben-Or
 
 
Chief Financial Officer
 

EX-99.1 2 exhibit_99-1.htm EXHIBIT 99.1

Exhibit 99.1

 
 
Sol-Gel Reports First Quarter 2025 Results
 
NESS ZIONA, Israel, May 23, 2025 (GLOBE NEWSWIRE) - Sol-Gel Technologies, Ltd. (NASDAQ: SLGL), a clinical-stage dermatology company, today announced financial results for the first quarter ended March 31, 2025.
 
Financial Results for the First Quarter Year Ended March 31st, 2025
 
Total revenue in the first quarter was $1 million compared to $0.5 million revenues for the same period in 2024.
 
Research and development expenses were $8.8 million compared to $5.3 million in the same period in 2024. The increase of $3.5 million was primarily attributed to an increase of $3.6 million due to expenses associated with supplier-led manufacturing development to support future commercialization of SGT-610, an increase of $0.5 million related to the commercialization of EPSOLAY and TWYNEO in territories outside of the U.S., offset by a decrease of $0.5 million in clinical trial expenses related to SGT-610.
 
General and administrative expenses were $1.3 million compared to $1.8 million for the same period in 2024. The decrease of $0.5 million was mainly attributed to a decrease in payroll and stock-based compensation expenses due to cost measures being taken in 2024.
 
Sol-Gel reported a net loss of $8.8 million for the first quarter of 2025 and of $3.2  basic and diluted loss per share, compared to a net loss of $6.3 million and a loss of $2.3 per basic and diluted share for the same period in 2024.
 
As of March 31, 2025, Sol-Gel had $16.9 million in cash, cash equivalents, and deposits and no marketable securities for a total balance of $16.9 million.
 
The Company expects its cash resources to fund cash requirements into the first quarter of 2027.

 
About Sol-Gel Technologies
 
Sol-Gel Technologies, Ltd. is a dermatology company focused on identifying, developing and commercializing or partnering drug products for the treatment of skin diseases. Sol-Gel developed TWYNEO which is approved by the FDA for the treatment of acne vulgaris in adults and pediatric patients nine years of age and older; and EPSOLAY, which is approved by the FDA for the treatment of inflammatory lesions of rosacea in adults.
 
The Company’s pipeline includes Orphan Drug candidate, SGT-610 under investigation for the prevention of new basal cell carcinomas in Gorlin syndrome patients, and also includes topical drug candidate SGT-210 under investigation for the treatment of rare skin keratodermas.
 
For additional information, please visit www.sol-gel.com.
 
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 our expected cash runway.  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, our ability to enter into further collaborations, lower than anticipated annual revenue income from new collaborations, a delay in the timing of our clinical trials, the success of our clinical trials, and an increase in our anticipated costs and expenses, as well as the following factors: (i) the adequacy of our financial and other resources, particularly in light of our history of recurring losses and the uncertainty regarding the adequacy of our liquidity to pursue our complete business objectives; (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 current war between Israel and Hamas and any deterioration of the war in Israel into a broader regional conflict involving Israel with other parties. 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 April 29, 2025, 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.
 
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SOL-GEL TECHNOLOGIES LTD.
CONDENSED CONSOLIDATED BALANCE SHEETS
(U.S. dollars in thousands)
(Unaudited)

   
December 31,
   
March 31,
 
   
2024
   
2025
 
Assets
           
CURRENT ASSETS:
           
Cash and cash equivalents
 
$
19,489
   
$
16,890
 
Bank deposits
   
12
     
12
 
Marketable securities
   
4,425
     
-
 
Accounts receivables
   
3,595
     
3,883
 
Prepaid expenses and other current assets
   
3,774
     
2,647
 
TOTAL CURRENT ASSETS
   
31,295
     
23,432
 
                 
NON-CURRENT ASSETS:
               
Restricted long-term deposits and cash equivalents
   
1,291
     
1,293
 
Long-term receivables
   
1,024
     
518
 
Property and equipment, net
   
202
     
183
 
Operating lease right-of-use assets
   
1,426
     
1,332
 
Other long-term assets
   
13
     
-
 
Funds in respect of employee rights upon retirement
   
595
     
305
 
TOTAL NON-CURRENT ASSETS
   
4,551
     
3,631
 
TOTAL ASSETS
 
$
35,846
   
$
27,063
 
Liabilities and shareholders' equity
               
CURRENT LIABILITIES:
               
Accounts payable
 
$
1,265
   
$
438
 
Other accounts payable
   
3,590
     
3,702
 
Current maturities of operating leases
   
430
     
433
 
TOTAL CURRENT LIABILITIES
   
5,285
     
4,573
 
                 
LONG-TERM LIABILITIES:
               
   Operating leases liabilities
   
878
     
746
 
Liability for employee rights upon retirement
   
833
     
363
 
Other long-term Liability
           
1,209
 
TOTAL LONG-TERM LIABILITIES
   
1,711
     
2,318
 
TOTAL LIABILITIES
   
6,996
     
6,891
 
                 
SHAREHOLDERS' EQUITY:
               
Ordinary shares, NIS 0.1 par value – authorized: 5,000,000 as of December 31, 2024 and March 31, 2025, respectively; issued and outstanding: 2,785,762 as of December 31, 2024 and March 31, 2025, respectively (*)
   
774
     
774
 
Additional paid-in capital
   
258,959
     
259,089
 
Accumulated deficit
   
(230,883
)
   
(239,691
)
TOTAL SHAREHOLDERS' EQUITY
   
28,850
     
20,172
 
TOTAL LIABILITIES AND SHAREHOLDERS' EQUITY
 
$
35,846
   
$
27,063
 

(*) All share amounts have been retroactively adjusted to reflect a 1-for-10 reverse share split.
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SOL-GEL TECHNOLOGIES LTD.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(U.S. dollars in thousands)
(Unaudited)

   
Three months ended
March 31
 
   
2024
   
2025
 
LICENSE REVENUES
 
$
466
   
$
1,031
 
RESEARCH AND DEVELOPMENT EXPENSES
   
5,345
     
8,843
 
GENERAL AND ADMINISTRATIVE EXPENSES
   
1,833
     
1,257
 
OPERATING LOSS
   
6,712
     
9,069
 
FINANCIAL INCOME, net
   
(368
)
   
(261
)
LOSS FOR THE PERIOD
   
6,344
     
8,808
 
BASIC AND DILUTED LOSS PER ORDINARY SHARE
   
2.3
     
3.2
 
WEIGHTED AVERAGE NUMBER OF SHARES*OUTSTANDING USED IN COMPUTATION OF BASIC AND DILUTED LOSS PER SHARE (*)
   
2,785,762
     
2,785,762
 

(*)All share amounts have been retroactively adjusted to reflect a 1-for-10 reverse share split.
 
Sol-Gel Contact:
Eyal Ben-Or
Chief Financial Officer
ir@sol-gel.com
+972-8-9313429
 
 

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