Exhibit 99.1

Press release dated March 30, 2022

Sol-Gel Technologies Reports Full Year 2021 Financial Results and Corporate Developments

 

 

 

 

 

 

NESS ZIONA, Israel, March 30, 2022, 2022 -- Sol-Gel Technologies, Ltd. (NASDAQ: SLGL), a dermatology company focused on identifying, developing and commercializing branded and generic topical drug products for the treatment of skin diseases, today announced financial results for the full year ended December 31, 2021, and provided recent corporate updates.

 

 

 

Alon Seri-Levy, Ph.D., Co-Founder and Chief Executive Officer of Sol-Gel, stated, “Pending the approval of EPSOLAY, Galderma will have the opportunity to promote both TWYNEO and EPSOLAY as products within its microencapsulation technology portfolio. We expect sales from both of these products to make a considerable contribution to Sol-Gel’s milestone revenue stream over time. At the same time, we’ve been prudent to immediately monetize our generics franchise to maximize the development of our high-value early-stage assets.”

 

Dr. Seri-Levy continued, “In parallel, we are excited to advance our innovative formulations of SGT-310 and SGT-510 in the second half of 2022 and view these products as future growth drivers for our company.”

 

Financial Results for the Year Ended December 31, 2021

 

Total revenue was $31.3 million, which consisted of $7.5 million of licensing revenue and $23.8 million of collaboration revenue, compared to collaboration revenues of $8.8 million in 2020.

 

Research and development expenses were $20.4 million compared to $27.9 million in 2020. The decrease of $7.5 million was mainly attributed to a decrease of $6.4 million in clinical trial expenses, primarily related to the completion of the clinical trials of EPSOLAY and TWYNEO, a decrease of $0.6 million in payroll and expenses related to share-based compensation.

 

General and administrative expenses were $8.5 million in 2021 compared to $11.1 million in 2020. The decrease of $2.6 million was mainly attributed to a decrease of $3.0 million in commercialization expenses.

 

Sol-Gel reported net income of $3.2 million in 2021 and earnings of $0.14 per basic and diluted share, compared to loss of $29.3 million and loss of $1.30 per basic and diluted share in 2020.

 

As of December 31, 2021, Sol-Gel had $41.5 million in cash, cash equivalents and deposits, and $1.7 million in marketable securities for a total balance of $43.2 million. As a result of our agreements with Galderma regarding EPSOLAY and TWYNEO and the agreement with Padagis, the Company expects that its cash resources will enable funding of operational and capital expenditure requirements through the end of 2023, assuming the timely approval of EPSOLAY. As of March 28, 2022, Sol-Gel had $31.6 million in cash, cash equivalents and deposits, and $6.2 million in marketable securities, for a total balance of $37.8 million.  

 

About TWYNEO

 

TWYNEO is a topical cream containing a fixed‑dose combination of tretinoin, 0.1%, and benzoyl peroxide, 3%, for the treatment of acne vulgaris in adults and pediatric patients nine years of age and older. TWYNEO is the first acne treatment that contains a fixed‑dose combination of benzoyl peroxide and tretinoin. Tretinoin and benzoyl peroxide are widely prescribed separately for acne vulgaris; however, benzoyl peroxide causes degradation of the tretinoin molecule, thereby potentially reducing its effectiveness if used at the same time or combined in the same formulation. TWYNEO uses silica (silicon dioxide) core shell structures to separately microencapsulate tretinoin crystals and benzoyl peroxide crystals enabling inclusion of the two active ingredients in the same cream.

 

About EPSOLAY

 

EPSOLAY is a topical cream containing benzoyl peroxide, 5%, under FDA review for the treatment of inflammatory lesions of rosacea in adults. EPSOLAY utilizes a proprietary technology to encapsulate benzoyl peroxide within silica-based microcapsules to create a barrier between the medication and the skin. The silica-based shell is designed to slowly release benzoyl peroxide over time to provide a favorable efficacy and safety profile. EPSOLAY is protected by granted patents until 2040.

 

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 commercial launch of TWYNEO, the regulatory approval of EPSOLAY, our expected cash runway, and the benefits we expect to receive under our agreement with Galderma. These forward-looking statements include information about possible or assumed future results of our business, financial condition, results of operations, liquidity, plans and objectives. 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 that we will not receive all of the anticipated benefits under our agreement with Galderma, the risk of a delay in the commercial availability of TWYNEO and/or EPSOLAY, the risk that TWYNEO will not provide treatment to the number of patients anticipated, risks relating to the effects of COVID‑19 (coronavirus) 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 ability to commercialize our pharmaceutical product candidates; (vi) our ability to obtain and maintain adequate protection of our intellectual property; (vii) our ability to manufacture our product candidates in commercial quantities, at an adequate quality or at an acceptable cost; (viii) our 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, Europe or Israel; and (xv) loss or retirement of key executives and research scientists. These 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 4, 2021 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.

 

For further information, please contact:

 

SOL-GEL TECHNOLOGIES LTD.

CONSOLIDATED BALANCE SHEETS

(U.S. dollars in thousands, except share and per share data)

		December 31
		2020				2021
Assets
CURRENT ASSETS:
Cash and cash equivalents		$	7,122			$	20,085
Bank deposits			21,400				21,448
Marketable securities			21,652				1,709
Receivables from collaborative arrangements			2,153				13,065
Prepaid expenses and other current assets			1,074				800
TOTAL CURRENT ASSETS			53,401				57,107
NON-CURRENT ASSETS:
Long-term receivables from collaborative arrangements			-				7,402
Restricted long-term deposits and cash			1,293				1,298
Property and equipment, net			1,817				1,051
Operating lease right-of-use assets			1,896				1,501
Funds in respect of employee rights upon retirement			754				830
TOTAL NON-CURRENT ASSETS			5,760				12,082
TOTAL ASSETS		$	59,161			$	69,189
Liabilities and shareholders' equity
CURRENT LIABILITIES:
Accounts payable		$	1,203			$	766
Other accounts payable			4,088				10,145
Current maturities of operating leases			673				781
TOTAL CURRENT LIABILITIES			5,964				11,692
LONG-TERM LIABILITIES:
Operating leases liabilities			1,299				810
Liability for employee rights upon retirement			1,049				1,093
TOTAL LONG-TERM LIABILITIES			2,348				1,903
COMMITMENTS
TOTAL LIABILITIES			8,312				13,595
SHAREHOLDERS' EQUITY:
Ordinary shares, NIS 0.1 par value – authorized: 50,000,000 as of December 31, 2020 and 2021, respectively; issued and outstanding: 23,000,782 and 23,126,804 as of December 31, 2020 and December 31, 2021, respectively			635				638
Additional paid-in capital			231,577				233,098
Accumulated deficit			(181,363	)			(178,142	)
TOTAL SHAREHOLDERS' EQUITY			50,849				55,594
TOTAL LIABILITIES AND SHAREHOLDERS' EQUITY		$	59,161				69,189

SOL-GEL TECHNOLOGIES LTD.

CONSOLIDATED STATEMENTS OF OPERATIONS

(U.S. dollars in thousands, except share and per share data)

---