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BioWorld - Friday, April 17, 2026
Home » Topics » Disease categories and therapies » Dermatologic

Dermatologic
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Dermasensor device

Dermasensor granted FDA clearance for skin cancer ID

Jan. 17, 2024
By Annette Boyle
Dermasensor Inc. received U.S. FDA clearance for its non-invasive skin cancer evaluation device that provides quantitative identification of all skin cancer types at the point of care and within seconds. The point-and-click device is designed to facilitate detection of skin cancers by primary care physicians (PCPs) and speed the time to diagnosis and treatment.
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Layoff, shutdown illustration

Lirentelimab out on failed phase II data; Allakos restructures

Jan. 16, 2024
By Karen Carey
Allakos Inc. terminated all development of its lead drug, anti-Siglec-8 antibody lirentelimab (AK-002), and is cutting its workforce in half, following phase II failures for atopic dermatitis and chronic spontaneous urticaria. The San Carlos, Calif.-based company will now focus on phase I trials for anti-Siglec-6 antibody AK-006 as part of a restructuring that stretches the runway into mid-2026. Shares (NASDAQ:ALLK) sank by 60.2%, down $1.80, to close at $1.19 on Jan. 16.
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Skin, tissue layer illustration
Dermatologic

OQL-025 cleared to enter clinic for EGFR inhibitor-induced rash

Jan. 5, 2024
Onquality Pharmaceuticals LLC has obtained IND clearance from the FDA for OQL-025 to treat epidermal growth factor receptor (EGFR) inhibitor-induced acneiform rash, a common toxicity affecting patients treated with EGFR inhibitor therapy for various cancers.
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3D illustration of a chain of amino acid or biomolecules called protein
Immune

Kymera Therapeutics unveils first-in-class oral degrader immunology programs

Jan. 5, 2024
Kymera Therapeutics Inc. has unveiled two new first-in-class oral degrader programs for immune-mediated diseases: KT-621, a STAT6 degrader, and KT-294, a TYK2 degrader.
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Dermatologic

Activon discovers new ROS production inhibitors

Jan. 4, 2024
Activon Co. Ltd. has described compounds acting as reactive oxygen species (ROS) production inhibitors reported to be useful for the treatment of aging, atopic dermatitis, cardiovascular disorders, cancer, hepatitis, hepatobiliary diseases, neurodegeneration and rheumatoid arthritis.
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3D illustration of the cross-section of skin layers with atopic dermatitis
Dermatologic

Tissue-specific actions of JAK1 call for nuanced therapeutic approach

Jan. 2, 2024
By Subhasree Nag
JAK1 signaling promotes skin inflammation and is a major therapeutic target for atopic dermatitis-related itching. But in a study appearing in the Jan. 4, 2024, print issue of Cell after earlier publication online, researchers at the Icahn School of Medicine at Mount Sinai, led by dermatologist Brian Kim, found that intrinsic JAK1 signaling in sensory neurons had an immunoprotective effect in the lung. The findings suggest a more precise and personalized approach is required to potentially expand JAK inhibitor use to a wider range of allergy and inflammatory disorders.
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Lab glassware and scientist
Gastrointestinal

Equillium to advance EQ-302 in place of EQ-102 for gastrointestinal and skin diseases

Dec. 22, 2023
Equillium Inc. has announced that it intends to advance EQ-302, a preclinical orally delivered multi-cytokine inhibitor of IL-15 and IL-21, in place of further clinical development of EQ-102.
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Neurology/Psychiatric

Sudo raises series B to advance TYK2 inhibitors for MS, psoriasis

Dec. 21, 2023
Sudo Biosciences Inc. has closed a $116 million series B financing, with the funding raised to be used to advance two investigational TYK2 candidates into the clinic in 2024.
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No forwarding Address: Argenx’s efgartigimod fails to deliver in pemphigus phase III

Dec. 20, 2023
By Randy Osborne
Argenx SE CEO Tim Van Hauwermeiren said that, with subcutaneous efgartigimod (efgartigimod alfa and hyaluronidase-qvfc) in pemphigus, the company is “facing a situation where, even with a strong scientific hypothesis and well-executed trial, we encountered the unknown-unknown,” and the phase III experiment failed. “We are committed to doubling down” on the execution of the firm’s business plan, he added.
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Chiesi’s Filsuvez finally clears FDA hurdle, approved for rare skin diseases

Dec. 19, 2023
By Jennifer Boggs
The data package for Filsuvez (birch triterpenes), a topical gel aimed at treating partial thickness wounds, satisfied U.S. reviewers the second time around. Chiesi Group said the FDA approved the treatment Dec. 19 for use in patients 6 months and older with rare blistering skin diseases junctional epidermolysis bullosa and dystrophic epidermolysis bullosa.
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