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Milestone Alert: First Subject Dosed in Phase 2b Vitiligo Trial of Novel BET Inhibitor

The Dermatology Digest

Check out TDD’s one-on-one interview with Iain Stuart, PhD , Chief Scientific Officer at Vyne Therapeutics. The randomized, double-blind, vehicle-controlled trial will evaluate the safety and efficacy of once-daily VYN201 topical gel in three dose cohorts (1%, 2% and 3% concentrations) compared to vehicle for 24 weeks.

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Exosomes vs PRP: Transform Your Skin Care Routine

Kim Gallo Esthetics

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. Effectiveness and Safety of Exosomes Exosomes have shown incredible potential in skin rejuvenation.

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PsO Pipeline Watch: Alumis Initiates Phase 3 Clinical Program Evaluating Its Oral TYK2 Inhibitor in Moderate-to-Severe Plaque PsO

The Dermatology Digest

Key secondary endpoints will include PASI 90, PASI 100 and sPGA 0 measured at Weeks 16 and 24, and safety and tolerability. Patients completing Week 24 will have the opportunity to participate in a long-term extension (LTE) trial, ONWARD3, that will evaluate durability and maintenance of response and long-term safety.

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Who’s Holding the Needle?

North Dallas Dermatology Associates

One misconception is cosmetic procedures are the same everywhere, from a local spa to a board-certified physician’s office. Safety Concerns and Potential Adverse Effects Another crucial consideration in evaluating where to have your cosmetic procedure performed is the ability to manage potential adverse effects.

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La Roche-Posay and the Edge Launch Immersive Color Exhibit in NYC

The Dermatology Digest

Whether it’s your first visit to the city or an annual tradition, SHADES at Edge offers a fresh, imaginative way to take in the 360 views of our iconic skyline like never before,” says Francesca Merlino, Chief Commercial Officer at Hudson Yards Experiences, in a news release.

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Rosacea Pipeline Watch: FDA Accepts Journey Medical’s NDA for DFD-29

The Dermatology Digest

The Phase 3 clinical trials achieved all co-primary and secondary endpoints, and subjects completed the 16-week treatment with no significant safety issues.

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Phase 2 Data: Extra-strength Jeuveau Smooths Frown Lines for Up to 6 Months

The Dermatology Digest

The safety profile was similar across all three arms and overall, 88.9% of adverse events were rated as mild and no serious adverse events were identified. The study appears in the Aesthetic Surgery Journa l. “The The study appears in the Aesthetic Surgery Journa l.

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