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BioWorld - Wednesday, February 25, 2026
Home » Topics » Disease categories and therapies » Dermatologic

Dermatologic
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NTLA-2002 shows promising preclinical results in a partial hepatectomy-induced HAE model

March 3, 2022

Targeting MRGPRX2-mediated mast cell activation as a therapeutic strategy for atopic dermatitis

March 1, 2022

Repertoire Immune Medicines and UMass Chan collaborate to understand immune causes of vitiligo

Feb. 18, 2022

Financing at Third Harmonic Bio to support development of oral KIT inhibitor THB-001

Feb. 16, 2022

TYK2 click-through? Other players watch, wait for BMS PDUFA date

Feb. 14, 2022
By Randy Osborne

As investors await the Sept. 10 PDUFA date for deucravacitinib from Bristol Myers Squibb Co. (BMS) in psoriasis, handicappers continue to weigh the odds of other tyrosine kinase 2 (TYK2) inhibitors, and ponder what a regulatory victory – or defeat – might mean for the space.


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New plasma kallikrein inhibitors identified at Merck Sharp & Dohme

Feb. 4, 2022

Therapy for ultra-rare XLHED edges closer as pivotal trial begins

Feb. 2, 2022
By Richard Staines
The ultra-rare skin disease X-linked hypohidrotic ectodermal dysplasia (XLHED) can be a heavy burden for children, affecting structures in the skin including sweat glands, respiratory glands, and hair as well as teeth. Though lacking a specific treatment to date, a pivotal clinical trial planned by the Geneva-based nonprofit Esperare Foundation and Pierre Fabre SA could now help bring one about.
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Almirall signs agreements with Ablexis and AliviaMab to support work in dermatology

Feb. 1, 2022

Almirall and IRB Barcelona collaborate on molecular glue degraders for skin diseases

Jan. 19, 2022

Abbvie, Pfizer JAK inhibitors win refractory atopic dermatitis approvals at FDA

Jan. 18, 2022
By Michael Fitzhugh
Two Janus kinase (JAK) inhibitors, Abbvie Inc.'s Rinvoq (upadacitinib) and Pfizer Inc.'s Cibinqo (abrocitinib), have won U.S. FDA approvals for the treatment of people with moderate to severe atopic dermatitis. Reviews of both products for the indication were delayed due to FDA concerns about class risks. Accordingly, each is labeled with a boxed warning regarding risks of serious infection, mortality, malignancy, major adverse cardiovascular events and thrombosis.
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