News

The Trump administration’s proposed cuts at the National Institutes of Health and Food and Drug Administration could lower ...
The president's proposed budget cuts to the NIH would eventually result in fewer drugs on the market, the U.S. Congressional ...
Researchers are building on the success of CAR T therapy in blood cancers to explore its use in clear cell renal cell ...
Aldeyra Therapeutics (NASDAQ:ALDX) announced on Thursday that the U.S. Food and Drug Administration (FDA) accepted for review ...
An FDA advisory panel will meet July 18 to consider a supplemental new drug application for the antipsychotic brexpiprazole, ...
The FDA accepted Aldeyra's resubmitted NDA for reproxalap after previous rejections due to efficacy concerns, despite no ...
The new drug application is supported by 48-week data from the Phase III MK-8591A-051 and MK-8591A-052 trials, which showed ...
Supporters believe that FDA approval will make the drug more accessible. Right now, traditional psilocybin therapy offered at healing centers in the state is not covered by insurance.
FDA grants priority review to TAR-200, which demonstrated an 82% complete response in high-risk bladder cancer unresponsive ...
A new report looks at hiring trends © 2025 American City Business Journals. All rights reserved. Use of and/or registration ...
CDSCO revises guidance document on export NOC for unapproved, approved new drugs: Gireesh Babu, New Delhi Friday, July 18, ...
The Food and Drug Administration (FDA) has accepted the New Drug Application for doravirine/islatravir (DOR/ISL) for adults with virologically-suppressed HIV-1 infection.