Sol-Gel Technologies to Participate in Upcoming LifeSci Partners Corporate Access Event and H.C. Wainwright BioConnect 2022 Healthcare Conference
Sol-Gel Technologies (Nasdaq: SLGL) announced its participation in two virtual conferences: the LifeSci Partners 11th Annual Corporate Access Event on January 5, 2022, featuring 1-on-1 meetings, and the H.C. Wainwright BioConnect 2022 Healthcare Conference, with a corporate presentation webcast available from January 10-13, 2022. The company focuses on developing topical drug products for skin diseases, leveraging its microencapsulation technology. The FDA is set to conduct a pre-approval inspection for its product EPSOLAY in February 2022, aiming for commercialization with Galderma.
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NESS ZIONA, Israel, Dec. 22, 2021 (GLOBE NEWSWIRE) -- Sol-Gel Technologies, Ltd. (Nasdaq: SLGL), a clinical-stage dermatology company focused on identifying, developing and commercializing branded and generic topical drug products for the treatment of skin diseases, today announced that the Company will participate in the LifeSci Partners 11th Annual Corporate Access Event and the H.C. Wainwright BioConnect Conference, both of which will be held virtually.
Event details are as follows:
LifeSci Partners 11th Annual Corporate Access Event | |
Format | 1-on-1 meetings |
Date: | January 5, 2022 |
Registration | Link |
H.C. Wainwright BioConnect 2022 Healthcare Conference | |
Format | Webcast of corporate presentation |
Date: | Webcast on demand starting at 7:00 am ET January 10 through January 13, 2022 |
Registration | Link |
About Sol-Gel Technologies
Sol-Gel is a dermatology company focused on identifying, developing and commercializing branded and generic topical drug products for the treatment of skin diseases. Sol‑Gel leverages its proprietary microencapsulation technology platform for TWYNEO, which is FDA approved for the treatment of acne vulgaris in adults and pediatric patients nine years of age and older; and EPSOLAY, under investigation for the treatment of inflammatory lesions of rosacea with an NDA filed with the FDA and a PDUFA goal date that was set for April 26, 2021. Action on the NDA for EPSOLAY has not yet been taken due to the inability of the FDA to conduct a pre‑approval inspection of the production site of EPSOLAY as a result of COVID‑19 travel restrictions. On December 21, 2021, Sol-Gel announced that FDA has updated Sol-Gel the pre-approval inspection for EPSOLAY will occur the week of February 14, 2022. Both product candidates are exclusively licensed for U.S. commercialization with Galderma. The Company’s pipeline also includes early-stage topical drug candidates SGT-210 (erlotinib gel) under investigation for the treatment of palmoplantar keratoderma, SGT-310 (tapinarof cream,
Contact:
Irina Koffler
Investor relations, LifeSci Advisors
ikoffler@lifesciadvisors.com
+1 917 734 7387
Sol-Gel Technologies
Gilad Mamlok
Chief Financial Officer
gilad.mamlok@sol-gel.com
FAQ
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