Celltrion, Inc. today announced the U.S. Food and Drug Administration (FDA) has approved a new presentation of OMLYCLO® (omalizumab-igec), the first and only biosimilar designated as interchangeable ...
Drug approvals this year have reflected the trend in clinical development of biologics shifting from intravenous to ...
Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced that the European Commission (EC) ...
Pharmaceutical Technology on MSN
Eisai seeks PMDA approval for subcutaneous Leqembi in Japan
If approved, patients could self-administer a weekly dose at home as an alternative to hospital intravenous dosing.
The US drug regulator has approved the Armlupeg (pegfilgrastim-unne) 6mg / 0.6 ml injection for subcutaneous use in a ...
This is the first and only subcutaneous immune checkpoint inhibitor in Europe that a health care provider can administer in ...
Eisai seeks Japanese PMDA approval for subcutaneous formulation of Leqembi to treat early Alzheimer’s disease: Tokyo Monday, December 1, 2025, 14:00 Hrs [IST] Eisai Co., Ltd. an ...
Eisai has submitted a new drug application to Japan’s Pharmaceuticals and Medical Devices Agency for a subcutaneous ...
The subcutaneous formulation of toripalimab demonstrated noninferior pharmacokinetics compared to the intravenous version in ...
If approved, ReadyFlow Autoinjector would deliver an IV-equivalent diuretic dose (subcutaneous furosemide injection 80 mg/ml) in under 10 ...
Lunsumio provides high rates of deep and long-lasting responses in third-line and later follicular lymphoma, a disease that ...
Does Weight Loss Medication Work? Key takeaways Weight loss medications work for many people. They can help those with ...
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