Beremagene geperpavec topical, marketed under the brand name Vyjuvek, is an FDA-approved medication for treating wounds caused by dystrophic epidermolysis bullosa (DEB).

Roche disclosed today that the European Commission has given the green light to Vabysmo® (faricimab) .

Perfluorohexyloctane ophthalmic, marketed under the brand name Miebo, is an FDA-approved medication for treating dry eye disease.

Galderma has successfully completed the European decentralized procedure, leading to a favorable decision for RelfydessTM.

Fezolinetant, sold under the brand name Veozah, was approved by the FDA on May 12, 2023.

Compugen has announced that the U.S. Food and Drug Administration has approved the investigational new drug application to begin a Phase 1 trial for COM503.

The FDA approved Arexvy on May 3, 2023. It is the first respiratory syncytial virus (RSV) vaccine approved for older adults.

Alpha Cognition has reported that the U.S. Food and Drug Administration has given the green light to ZUNVEYL® (benzgalantamine).

The FDA approved VOWST on April 26, 2023, for the prevention of recurrence of Clostridioides difficile infection (CDI) in adults following antibacterial treatment for recurrent CDI.

NewAmsterdam Pharma Announces Positive Topline Data from Pivotal Phase 3 BROOKLYN Clinical Trial Evaluating Obicetrapib in Patients with Heterozygous Familial Hypercholesterolemia.

Yes, Tofersen, marketed under the brand name Qalsody, received FDA approval on April 25, 2023.

CStone Announces European Commission Approval of Sugemalimab (Cejemly®) as First-Line Treatment for Non-Small Cell Lung Cancer.