Mitapivat (Pyrukynd) was approved by the FDA on February 17, 2022.

Novo Holdings spearheads $100 million Series C investment in Asceneuron to propel innovative Alzheimer’s treatment forward.

The FDA approved Sutimlimab (Enjaymo) on February 4, 2022. This approval marked an important development for patients with CAD.

Biosyngen's BRG01 moves to Phase II trial, pioneering autologous EBV-specific CAR-T for recurrent/metastatic nasopharyngeal carcinoma solid tumors.

Faricimab ophthalmic was approved by the FDA on January 28, 2022. This approval covers its use in adults for treating neovascular age-related macular degeneration and diabetic macular edema.

Evommune, Inc. reported positive findings from its initial proof-of-concept study in humans with EVO756.

Tebentafusp received FDA approval on January 25, 2022. It is a prescription medication used to treat adults with uveal melanoma.

Jul 18th latest updates in the global new drug development field, including progress in new drug research and development, transaction information, and partnership developments.

Daridorexant was approved by the U.S. Food and Drug Administration (FDA) on January 7, 2022, for the treatment of insomnia in adults who have difficulty falling asleep or staying asleep.

CatalYm has reported the successful closure of their Series D financing, raising $150 million.

The FDA approved Recorlev on December 30, 2021, for the treatment of endogenous hypercortisolemia in patients with Cushing's syndrome when surgery is not an option or has not been curative.

NexThera Co., Ltd. revealed that it has filed a Phase 1/2a Investigational New Drug application with the U.S. Food and Drug Administration for NT-101.