Sol-Gel Technologies Reports Third Quarter 2023 Financial Results and Provides Corporate Update
- Sol-Gel on track to advance Orphan Drug candidate, SGT-610 (patidegib) for Gorlin syndrome into Phase 3 testing in late 2023
- Gorlin Syndrome KOL event to be held on
December 6, 2023
- Sol-Gel maintains cash runway into the second half of 2025
“We are on track to begin pivotal Phase 3 testing for our Breakthrough-designated, Orphan Drug candidate, SGT-610, or patidegib, for the prevention of basal cell carcinoma in subjects having Gorlin syndrome, which we are planning to initiate this quarter. We anticipate this candidate will have a market potential of over $300 million as a first-ever therapy in a patient population that currently has no approved therapies,” stated Alon Seri Levy, Ph.D., Chief Executive Officer of Sol-Gel.
“As we announced last quarter, SGT-610 is our primary focus due to its promising potential, and we have optimized the Phase 3 trial design and enrollment criteria to maximize the probability of success,” he added. “Additionally, we continue to have discussions with prospective partners to secure new international licenses for our marketed products, TWYNEO and EPSOLAY, to generate non-dilutive capital.”
Q3 2023 and Recent Corporate Developments
- Based on Sol-Gel’s adoption of cost-saving measures announced in the second quarter, the Company continues to maintain its cash runway into the second half of 2025.
- In the third quarter of 2023, TWYNEO maintained a high recurring base of prescribers compared to the second quarter. In addition, TWYNEO’s market access position remains strong with broad commercial formulary coverage on CVS/Caremark, Express Scripts and Optum plans.
- According to
IQVIAdata, total prescriptions of TWYNEO written in the third quarter approached 27,000 with total prescriptions since launch surpassing 189,000.
- According to IQVIA data, there have been over 13,000 prescriptions of EPSOLAY written in the third quarter of 2023 and over 65,000 prescriptions written to date.
Sol-Gel'soperations remain on-going despite the current war.
- The Company plans to host a KOL event on
December 6, 2023to discuss Gorlin syndrome and the SGT-610 Phase 3 study. Further details are forthcoming and will be available in the Investors/Events & Presentations section of the www.sol-gel.com website.
Financial Results for the Quarter Ended September 30, 2023
Total revenue in the three months was $0.2 million, which primarily consisted of licensing revenues from Galderma.
Research and development expenses were $4.7 million compared to $2.0 million for the same period in 2022. The increase of $2.7 million was primarily attributed to an increase of $2.0 million related to the continuing development of SGT-610.
General and administrative expenses for the third quarter of 2023 were $1.9 million compared to $1.8 million for the same period in 2022.
Sol-Gel reported a net loss of $5.7 million for the third quarter of 2023 and a loss of $0.21 per basic and diluted share, compared to a net loss of $3.4 million and a net loss of
About Gorlin Syndrome and SGT-610
SGT-610, a hedgehog signaling pathway blocker, has the potential to be the first ever treatment for Gorlin syndrome, if approved. Gorlin syndrome, an autosomal dominant genetic disorder affecting approximately 1 in 27,000-31,000 people in the U.S., is mostly caused by inheritance of one defective copy of the tumor suppressor patched homolog 1 (PTCH1) gene. Normally, the PTCH1 gene blocks the smoothened, frizzle class receptor (SMO) gene, turning off the hedgehog signaling pathway when it is not needed. Mutations in the PTCH1 gene may cause a loss of PTCH1 function, release of SMO, and may allow basal cell carcinoma (BCC) tumor cells to divide uncontrollably. Patidegib, the active substance in SGT-610, is designed to block the SMO signal, thus, allowing cells to function normally and reducing the production of new tumors.
TWYNEO (tretinoin and benzoyl peroxide) Cream, 0.1%/3% is used for the topical treatment of acne vulgaris in adults and pediatric patients 9 years of age and older.
TWYNEO utilizes a proprietary, patented technology where tretinoin and BPO are encapsulated within silica-based microcapsules to create a barrier between the medication and the skin. The patented microencapsulation technology in TWYNEO Cream segregates and envelopes the active ingredients in silica core shells (microcapsules) so that tretinoin is protected from the oxidizing effects of BPO, allowing the combination of both drugs into one product and gradual release onto the skin.
Sol-Gel Technologies received U.S. Food and Drug Administration (“FDA”) approval for TWYNEO Cream on July 27, 2021, and granted exclusive rights to Galderma to commercialize the treatment in the U.S.
EPSOLAY is a topical cream containing encapsulated benzoyl peroxide (BPO), 5%, for the treatment of inflammatory lesions of rosacea in adults. EPSOLAY utilizes a proprietary, patented technology to encapsulate BPO within silica-based microcapsules to create a barrier between the medication and the skin. The silica-based shell is designed to slowly release BPO over time to provide a tolerable and effective treatment.
Sol-Gel Technologies received FDA approval for EPSOLAY Cream on April 22, 2022, and granted exclusive rights to Galderma to commercialize the treatment in the U.S.
About Sol-Gel Technologies
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.
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, the timing of beginning the Phase 3 clinical trial of SGT-610, success of any clinical studies, and obtaining regulatory approval for our product candidates including SGT-610; our expected cash runway; our ability to out-license additional international rights for TWYNEO and EPSOLAY; and the commercial acceptance and profitability 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, a delay in the timing of our clinical trials, including the timing of beginning the Phase 3 clinical trial of SGT-610, 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, 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
For further information, please contact:
Investor relations, LifeSci Advisors
+1 917 734 7387
Chief Financial Officer
CONSOLIDATED BALANCE SHEETS
|A s s e t s|
|Cash and cash equivalents||$||12,448||$||14,135|
|Receivables from collaborative arrangements||7,858||-|
|Prepaid expenses and other current assets||1,571||2,154|
|TOTAL CURRENT ASSETS||43,055||45,472|
|Restricted long-term deposits and cash||1,288||1,290|
|Property and equipment, net||660||499|
|Operating lease right-of-use assets||876||1,921|
|Funds in respect of employee rights upon retirement||749||680|
|TOTAL NON-CURRENT ASSETS||3,573||4,390|
|Liabilities and shareholders' equity|
|Other accounts payable||2,360||3,806|
|Current maturities of operating leases||718||467|
|TOTAL CURRENT LIABILITIES||3,329||4,507|
|Operating leases liabilities||54||1,222|
|Liability for employee rights upon retirement||1,032||1,007|
|TOTAL LONG-TERM LIABILITIES||1,086||2,229|
|Additional paid-in capital||234,640||257,819|
|TOTAL SHAREHOLDERS' EQUITY||42,213||43,126|
|TOTAL LIABILITIES AND SHAREHOLDERS' EQUITY||$||46,628||$||49,862|
CONSOLIDATED STATEMENTS OF OPERATIONS
|Nine months ended
||Three months ended
|RESEARCH AND DEVELOPMENT EXPENSES||8,465||19,370||2,042||4,672|
|GENERAL AND ADMINISTRATIVE EXPENSES||5,357||5,649||1,844||1,862|
|OTHER INCOME, net||-||14||-||14|
|FINANCIAL INCOME, net||901||1,496||218||596|
|LOSS FOR THE PERIOD||$||(9,138||)||$||(22,402||)||$||(3,407||)||$||(5,711||)|
|BASIC AND DILUTED LOSS PER ORDINARY SHARE||(0.40||)||(0.84||)||(0.15||)||(0.21||)|
|WEIGHTED AVERAGE NUMBER OF SHARES OUTSTANDING USED IN COMPUTATION OF BASIC AND DILUTED LOSS PER SHARE||23,128,469||26,826,458||23,129,469||27,844,212|
Source: Sol-Gel Technologies Ltd.