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Exosomes vs PRP: Transform Your Skin Care Routine

Kim Gallo Esthetics

Two groundbreaking treatments making waves are Exosomes and Platelet-Rich Plasma (PRP) therapies. What is Platelet-Rich Plasma (PRP) Therapy? Additionally, PRP carries more health risks due to the requirement of an in-office blood draw, which poses potential risks of infection and cross-contamination.

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U.S. FDA Grants Orphan Drug Designation for Restem’s ULSC Program for the Treatment of Dermatomyositis and Polymyositis

The Dermatology Digest

Restem’s ULSC therapy has shown promising results in early clinical trials, demonstrating safety, tolerability and initial clinically significant improvements, as well as the potential to significantly reduce the need for steroid use in patients. The estimated incidence of PM/DM is approximately 5 to 22 cases per 100,000 individuals.

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U.S FDA Approves Mirdametinib (Gomekli, SpringWorks) for Adult and Pediatric Patients With NF1-PN

The Dermatology Digest

It was very encouraging in the ReNeu trial to see that Gomekli provided deep and durable responses, with a manageable safety profile that enabled patients to stay on therapy. Gomekli demonstrated a manageable safety and tolerability profile.

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Palvella Therapeutics’ QTORIN Rapamycin 3.9% Anhydrous Gel Shows Promise for Microcystic LMs

The Dermatology Digest

Food and Drug Administration (FDA)-approved therapies for microcystic LMs. The FDA has granted Breakthrough Therapy Designation, Fast Track Designation, and Orphan Drug Designation to QTORIN rapamycin for the treatment of microcystic LMs. million from FDAs Office of Orphan Products Development. There are no U.S.

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Using CO2 Laser + Other Modalities to Treat Skin Pigmentation

Lipgloss and Aftershave

Active Ingredients in Pigmentation Therapy In-office treatments are complemented by topical agents that help maintain results and prevent new pigmentation. These are some topical agents to enhance in-office treatments, maintaining and prolonging results through consistent home care. Dermatologic Therapy. Farris, P.

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Incyte’s Povorcitinib Hits Primary Endpoints in Phase 3 HS Studies

The Dermatology Digest

The overall safety profile of povorcitinib is consistent with previous data. No new safety signals were observed and both doses were well tolerated. Both studies include a 12-week double-blind, placebo-controlled treatment period, followed by a 42-week extension period and 30-day safety follow-up. 75mg: 40.6% 75mg: 42.3%

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Meet the First-ever Recipients of The Lupus Research Alliance’s Translational Bridge Award

The Dermatology Digest

. “The new Translational Bridge Award addresses a critical gap in lupus research, enabling scientists to bring their most promising ideas closer to people living with lupus,” says Teodora Staeva, PhD, LRA Vice President and Chief Scientific Officer, in a news release.