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BioWorld - Saturday, February 21, 2026
Home » Topics » Disease categories and therapies » Dermatologic

Dermatologic
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Pemphigus bids continue to bubble after Sanofi’s phase III fail

Sep. 20, 2021
By Randy Osborne
Sanofi SA’s high-profile phase III blow-up Sept. 9 with the oral BTK inhibitor rilzabrutinib in pemphigus brought fresh attention to the group of rare diseases – which cause blisters on the skin and mucous membranes throughout the body – and to players pushing for a new treatment.
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Jiangsu Chia Tai Tianqing Pharmaceutical Group patents antibodies binding IL-4RA

Sep. 20, 2021

JUN identified as a crucial regulator of pathological skin scarring via CD36

Sep. 15, 2021

Genfleet Therapeutics discovers RIP-1 inhibitors

Sep. 9, 2021
Man scratching arm

Forte's atopic dermatitis bet sours on phase II failure, toppling shares

Sep. 3, 2021
By Michael Fitzhugh
Shares of Forte Biosciences Inc. (NASDAQ:FBRX) touched a 52-week low, diving 82.3% to close at $5.06 on Sept. 3 after its sole candidate, FB-401, failed to make a statistically significant difference in improving the severity of atopic dermatitis. The result, contrasting starkly with a smaller positive trial, led CEO Paul Wagner to announce the company would quit development of the FDA fast-tracked asset, licensed from the U.S. National Institute of Allergy and Infectious Diseases.
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LEO Pharma's novel IL-17A/IL-17AR interaction modulator for the oral treatment of psoriasis

Sep. 3, 2021

New melanocortin receptor modulators presented by Palatin Technologies

Sep. 2, 2021

Phase II study of SHR-0302 in alopecia areata meets primary efficacy endpoint

Aug. 26, 2021

Data presented for Almirall's JAK inhibitor LAS-200019

Aug. 26, 2021
FDA Approved stamp

FDA approves Cara’s Korsuva for itching in hemodialysis patients

Aug. 24, 2021
By Richard Staines
The FDA has approved Korsuva (difelikefalin) from Cara Therapeutics Inc. for pruritis in patients undergoing hemodialysis, following a fast review. Korsuva is the first therapy approved by the FDA in the indication and is the first ever approval for the Stamford, Conn.-based company.
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