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BioWorld - Wednesday, December 24, 2025
Home » Topics » Disease categories and therapies » Dermatologic

Dermatologic
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FDA approves Klisyri for actinic keratosis on the face or scalp

Dec. 15, 2020

First patient dosed in phase II BLUEPRINT study of BLU-5937

Dec. 15, 2020

Hoth receives Australian clearance for phase Ib trial of BioLexa for atopic dermatitis

Dec. 11, 2020

AbbVie reports phase IIIb head-to-head data on upadacitinib in atopic dermatitis

Dec. 11, 2020

Pharvaris discovers B2 bradykinin receptor antagonists

Dec. 11, 2020

Positive topline data presented from phase Ib study of EDP-1815 in atopic dermatitis

Dec. 10, 2020
Dong-ki Lee, CEO, Olix

Olix nabs $38M for core pipeline and RNA synthesis GMP facility

Dec. 8, 2020
By Gina Lee
HONG KONG – Olix Pharmaceuticals Inc. has raised ₩41.5 billion (US$37.90 million) to support the company’s U.S. expansion and advance its pipeline globally.
Read More
Dong-ki Lee, CEO, Olix

Olix nabs $38M for core pipeline and RNA synthesis GMP facility

Dec. 4, 2020
By Gina Lee
HONG KONG – Olix Pharmaceuticals Inc. has raised ₩41.5 billion (US$37.90 million) to support the company’s U.S. expansion and advance its pipeline globally.
Read More
Orladeyo product packaging

Biocryst’s Orladeyo cleared for HAE, priced high; is oral appeal enough?

Dec. 4, 2020
By Randy Osborne
As expected, the FDA cleared Biocryst Pharmaceuticals Inc.’s oral, once-daily Orladeyo (berotralstat, formerly known as BCX-7353) for the prevention of hereditary angioedema (HAE) attacks. Last month, Biocryst, as part of its earnings report, said approvals of the compound, a kallikrein inhibitor evaluated by U.S. regulators without an advisory committee meeting, could come in Japan this month and in the EU by the first half of next year.
Read More

Arcutis presents data from long-term safety study of ARQ-151 in plaque psoriasis

Dec. 3, 2020
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