News|Articles|September 7, 2025

Top 5 Articles of the Week: August 31-September 5

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Key Takeaways

  • Laser therapies, including 1726-nm diode and fractional CO₂ lasers, show promise in acne management, offering high efficacy and minimal side effects.
  • AI tools in dermatology reduce administrative burdens but raise concerns due to insurers' use for claim denials, necessitating responsible integration.
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Explore the top headlines of the week, including insights on the latest clinical trials, therapeutic updates, and more.

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1. Laser Therapy Gains Ground in Acne Management

Acne vulgaris affects over 50 million people annually in the US, and while standard therapies remain the foundation of care, their limitations have driven interest in laser-based treatments. Visible light lasers such as pulsed-dye devices can reduce inflammatory lesions but carry pigmentation risks, while near-infrared Nd:YAG lasers have shown broad efficacy, especially in combination approaches. Newer 1726-nm diode lasers (AviClear, Accure) directly target sebaceous glands with response rates above 85% and minimal side effects, and fractional CO₂ lasers improve both active acne and scarring. Although more controlled, long-term studies are needed, lasers offer a promising non-pharmacologic option that may reduce antibiotic reliance and expand treatment choices for patients unresponsive to conventional therapies.

2. AI Trends in Dermatology: Talking With David Cotter, MD, PhD at DERM 2025

In a recent Dermatology Times interview, Las Vegas dermatologist David Cotter, MD, PhD, discussed the promise and pitfalls of AI in clinical practice. While AI tools like scribes and prior authorization assistants are reducing administrative burdens and streamlining patient access to treatments, Cotter warns that insurers are also using AI—often to deny claims at alarming rates. This dual use has sparked legal action, including class-action lawsuits against companies allegedly automating denials without proper review. Clinically, AI has potential in diagnostics, especially for skin cancer, but Cotter stresses it's not yet reliable as a standalone tool. Instead, he advocates for a collaborative approach: “man with machine.” Cotter urges fellow clinicians to embrace AI responsibly, integrating it into practice while remaining vigilant, saying, “The future is now… If we shy away from it, patients may experience harm.”

3. How Metabolic Science, Regenerative Medicine, and Biohacking are Transforming Aesthetics

At the DERM 2025 NP PA CME Conference in Las Vegas, Nevada, Suneel Chilukuri, MD, a board-certified dermatologist at Refresh Dermatology in Houston, Texas, spotlighted the convergence of metabolic science, regenerative medicine, and aesthetic dermatology. He emphasized the importance of interdisciplinary collaboration in the field, celebrating the meeting’s inclusive format that brings together physicians, nurse practitioners, physician assistants, and aestheticians. He praised the conference environment as one that fosters openness, accessibility to thought leaders, and the exchange of both clinical and aesthetic insights.

4. Mallia Aesthetics Completes Regulatory Milestones for Novel sCD83-Based Hair Growth Technology

Mallia Aesthetics GmbH, a German biopharmaceutical and cosmetics company, completed several developmental and regulatory steps toward the validation of MAL-838, the foundation of its upcoming hormone-free 8T3 product line targeting hair growth. These steps further establish the novel products’ readiness for the market later this year.

5. FDA Targets Whipped Sunscreens in Warning Letters

The FDA has issued warning letters to Supergoop and Vacation Inc. for marketing sunscreen mousse products without agency approval. While sunscreens are regulated as OTC drugs, only certain dosage forms—such as lotions, creams, gels, sprays, and sticks—are permitted under the current OTC monograph. Foam and mousse formats require specific FDA authorization, which has not been granted.

Supergoop’s “PLAY SPF 50 Body Mousse” and Vacation’s “Classic Whip” sunscreen line were cited as misbranded, with the FDA noting that Vacation’s whipped cream–style packaging also posed a risk of confusion with food products, particularly for children. Both companies must respond within 15 days or face potential enforcement actions, including seizure or injunction.

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