FDA to approve drug to treat autism symptoms Politico What is leucovorin? Researchers mixed on Trump, RFK Jr.’s potential answer to autism USA Today FDA Moves to Approve Little-Known Drug to Treat Autism Symptoms The Wall Street Journal FDA brings back GSK’s leucovorin drug that RFK Jr. touted as autism treatment statnews.com What is leucovorin? Inside the drug giving new hope to autism patients New …
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Merck wins FDA approval for subcutaneous Keytruda (MRK:NYSE) – Seeking Alpha
Merck wins FDA approval for subcutaneous Keytruda (MRK:NYSE) Seeking Alpha FDA OKs New Keytruda Shot for Cancer The New York Times EMA committee recommends approval for injectable version of Merck’s Keytruda Reuters Merck wins approval of subcutaneous Keytruda, in bid to extend life of world’s top-selling drug Endpoints News FDA Approves Subcutaneous Pembrolizumab for Solid Tumors OncLive Source link
Read More »FDA Approves Merck’s KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) Injection for Subcutaneous Use in Adults Across Most Solid Tumor Indications for KEYTRUDA® (pembrolizumab) – Merck.com
FDA Approves Merck’s KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) Injection for Subcutaneous Use in Adults Across Most Solid Tumor Indications for KEYTRUDA® (pembrolizumab) Merck.com FDA OKs New Keytruda Shot for Cancer The New York Times FDA Approves Subcutaneous Pembrolizumab for Solid Tumors OncLive US FDA approves Merck’s injectable version of blockbuster cancer therapy Keytruda Reuters Merck wins approval of subcutaneous Keytruda, in bid to …
Read More »FDA Grants Accelerated Approval to First Treatment for Barth Syndrome
For Immediate Release: September 19, 2025 Today, the U.S. Food and Drug Administration granted accelerated approval to Forzinity (elamipretide) injection as the first treatment for Barth syndrome, in patients weighing at least 30 kg. Barth syndrome is a rare, serious and life-threatening disease of the mitochondria (the energy-producing parts of cells). “The FDA remains committed to facilitating the development of …
Read More »US FDA approves Merck's injectable version of blockbuster cancer therapy Keytruda – Reuters
US FDA approves Merck’s injectable version of blockbuster cancer therapy Keytruda Reuters FDA OKs New Keytruda Shot for Cancer The New York Times FDA Approves Subcutaneous Pembrolizumab for Solid Tumors OncLive Merck wins approval of subcutaneous Keytruda, in bid to extend life of world’s top-selling drug Endpoints News Merck Wins US Approval of Easier-to-Use Version of Cancer Drug Keytruda Bloomberg.com Source link
Read More »FDA OKs New Keytruda Shot for Cancer – The New York Times
FDA OKs New Keytruda Shot for Cancer The New York Times FDA Approves Subcutaneous Pembrolizumab for Solid Tumors OncLive Merck wins approval of subcutaneous Keytruda, in bid to extend life of world’s top-selling drug Endpoints News Merck Wins US Approval of Easier-to-Use Version of Cancer Drug Keytruda Bloomberg.com US FDA approves Merck’s injectable version of blockbuster cancer therapy Keytruda Reuters Source link
Read More »What The FDA Says To Do If They’re In Your Kitchen
Kryuchka Yaroslav/Shutterstock One of the most dangerous materials to consume may have found its way into some Americans’ kitchens. The Food & Drug Administration (FDA) has just updated a list of pots and pans sold in the country that contain lead. The FDA has been cracking down on lead contaminants in food, …
Read More »FDA Warns About This Toxic Cookware — What to Know & Buy Instead
Check your kitchen cabinets: Some of your nonstick cookware may be potentially toxic, according to an update from the Food and Drug Administration (FDA). On Aug. 13 2025, the FDA first issued a warning about a list of imported nonstick cookware that may be leaching “significant levels” of lead. The organization recently updated the warning on Sept. 12, adding three …
Read More »Who can get a COVID-19 vaccine in Ohio? FDA restricts eligibility
CLEVELAND, Ohio — Last fall, all it took to get a COVID-19 vaccine was rolling up your sleeve. This year, pharmacies in Ohio and elsewhere will first ask if you’re 65 or older, or have underlying medical conditions putting you at risk for a severe case of the respiratory illness. That’s because the U.S. Food and Drug Administration has restricted …
Read More »FDA cracks down on prescription drug ads but lacks staff
WASHINGTON – In an unprecedented move, federal regulators published about 100 warning letters sent to pharmaceutical companies and health care providers, ordering them to stop or alter ads or other promotions the government considered misleading. The letters went to major drugmakers like Novartis and Eli Lilly, and to telehealth firms like Hims & Hers, shortly after the Trump administration announced the …
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