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Exosomes vs PRP: Transform Your Skin Care Routine

Kim Gallo Esthetics

If you buy through links on this page, we may earn a small commission In recent years, the beauty industry has been buzzing about the wonders of regenerative skin treatments, and with good reason. These treatments promise youthful, glowing skin using cutting-edge techniques. What is Platelet-Rich Plasma (PRP) Therapy?

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PHysicians & the esthetician

Southeastern Esthetics Institute

Estheticians must obtain written permission and treatment plans through the physician overseeing the practice, with monitoring by the physician of all notations within patient charts, products and modalities used, and any other thought process made throughout the duration of treatment.

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

The Dermatology Digest

Top-line data from the 24-week vehicle-controlled treatment period are expected in mid-2025. Check out TDD’s one-on-one interview with Iain Stuart, PhD , Chief Scientific Officer at Vyne Therapeutics. VYN201 is a novel pan-bromodomain and extra-terminal domain (BET) inhibitor designed for local administration.

Safety 73
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U.S. FDA Approves Bimekizumab-bkzx (Bimzelx, UCB) for HS

The Dermatology Digest

Food and Drug Administration (FDA) has approved bimekizumab-bkzx (Bimzelx, UCB) for the treatment of adults with moderate-to-severe hidradenitis suppurativa (HS). Today’s approval of bimekizumab-bkzx is an exciting time for the hidradenitis suppurativa community, offering a new possibility for the treatment of people in the U.S.

Safety 78
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Rosacea Pipeline Watch: FDA Accepts Journey Medical’s NDA for DFD-29

The Dermatology Digest

Food and Drug Administration (FDA) has accepted Journey Medical’s New Drug Application (NDA) for DFD-29 (Minocycline Hydrochloride Modified Release Capsules, 40 mg) for the treatment of inflammatory lesions and erythema of rosacea in adults. The FDA has set a Prescription Drug User Fee Act (PDUFA) goal date of November 4, 2024. “We

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Eye on Itch: Evommune Initiaties Phase I Study of EVO756 in CSU

The Dermatology Digest

By blocking MRGPRX2 activation and degranulation of mast cells, EVO756 has the potential to be a first-in-class oral treatment for a variety of mast cell-mediated diseases, including chronic spontaneous urticaria and inflammatory itch. Evommune, Inc.

Safety 74
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Arcutis’ Roflumilast Foam Continues to Impress in Seb Derm

The Dermatology Digest

Food and Drug Administration (FDA) for treatment of seborrheic dermatitis in adult and pediatric patients 9 years of age and older in December 2023. Zoryve foam was well-tolerated with a favorable safety and tolerability profile. There were no treatment-related Serious Adverse Events (SAEs). Zoryve foam was approved by the U.S.