
Dermatology Times April 2025 Recap
Key Takeaways
- Dupilumab is now approved for chronic spontaneous urticaria, marking a significant advancement in targeted therapy.
- AbbVie seeks FDA approval for TrenibotE, a novel botulinum toxin for glabellar lines.
Dermatology Times is looking back on the top stories in dermatology from the month of April.
Clearances, Approvals, Updates, and Recommendations
Dupilumab becomes the first targeted therapy approved for chronic spontaneous urticaria in more than a decade.
AbbVie seeks FDA approval for TrenibotE, a first-in-class botulinum toxin offering fast onset and short duration for glabellar lines.
The FDA approved pz-cel, a groundbreaking gene therapy for recessive dystrophic epidermolysis bullosa, transforming treatment options for patients.
Big Studies and Big Data
Tremfya is the first IL-23 inhibitor to significantly improve both symptoms and structural damage in active psoriatic arthritis.
A cross-sectional survey revealed that many patients with HS are dissatisfied with treatment options, with gaps in knowledge about FDA-approved therapies.
A new subgroup analysis revealed higher rates of clear or almost clear skin at week 16 vs placebo with a favorable safety profile.
The presentation, led by Amy Paller, MS, MD, highlighted the upcoming phase 3 SELVA study for microcystic lymphatic malformations.
Interim FDA-funded study results show HyBryte delivers rapid, sustained response and strong safety in early-stage CTCL patients.
New prospective data from the DECIDE study reinforce the role of the 31-GEP test in clinical decision-making.
A survey by LEO Pharma indicates widespread misunderstandings about chronic hand eczema, revealing significant emotional and occupational challenges for patients.
Market, Pharma, and Specialty News
Get a glimpse of the cutting-edge atopic dermatitis research, breakthroughs, and insights to be presented at the 7th RAD Annual Meeting, June 6-7, 2025.
Alphyn Biologics has dosed the first patient in a global phase 2b trial of zabalafin hydrogel for mild to moderate atopic dermatitis.
Evommune has initiated a global phase 2b trial of EVO756, a first-in-class MRGPRX2 antagonist, for moderate to severe CSU.
The funds will target programs for chronic pruritus, atopic dermatitis, and other inflammatory skin conditions.
Palvella has secured its 5th US patent for Qtorin rapamycin, extending intellectual property coverage to 2038 and advancing treatment for microcystic lymphatic malformations.
Pelthos and Channel Therapeutics will merge to form a new publicly traded entity focused on commercializing the first at-home treatment for molluscum.
VYNE Therapeutics paused its VYN202 trial for psoriasis due to an FDA-issued clinical hold.
Strides for Skin Health Equity
Nearly all patients saw improvements in small, medium, and large depressions on the cheeks and temples with just a singular treatment session.
Sherket Peterson, PhD, spoke to Dermatology Times about Allergan’s recent research and plan to launch a universal skin quality index.
Haut.AI’s new tool promotes inclusive and realistic conversations on the power of skincare products, according to the CEO.
JAK inhibitors show promise in treating alopecia areata among Black patients, highlighting the need for inclusive clinical research and equitable access to therapies.
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