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Atlanta Journal-Constitution1mon
Cancer drug shortage prompts Georgia lawmakers to raise issue with FDA
The FDA subsequently allowed imports of the cancer drug from China, from Qilu Pharmaceutical, whose version of the drug is unapproved in the U.S. Georgia’s elected officials are asking the FDA ...
WCJB on MSN
1d
Drug companies urge FDA to block Florida prescription imports
The state has been waiting nearly three years for the FDA to approve a Canadian Prescription Drug Import program ...
Scientific American
10d
Why There’s a Serious Cancer Drug Shortage, and How to Fix It
A cancer diagnosis is already devastating. It’s even more gut-wrenching when your doctor tells you that a drug shortage has ...
PMLiVE13d
FDA boosts collaboration with manufacturers to overcome ongoing cancer drug shortages
The US Food and Drug Administration (FDA) has increased its collaboration with cancer drug manufacturers in a bid to overcome the country’s ongoing drug shortage problem and reduce impacts on patients ...
STAT3d
FDA panel votes against GLP-1 therapy from former diabetes unicorn Intarcia
An advisory panel to the Food and Drug Administration unanimously voted against a diabetes implant from Intarcia Therapeutics — a former biotech unicorn that faltered after the FDA rejected said ...
Yahoo Finance13d
Iovance (IOVA) Up Despite FDA's Delayed Decision on Melanoma Drug
Iovance Biotherapeutics IOVA announced that the FDA has postponed the previously expected decision date, regarding the company’s biologics license application (BLA) for lifileucel, from Nov 25 ...
Everyday Health8d
FDA Approves Momelotinib (Ojjaara) for Myelofibrosis Patients With Anemia
The U.S. Food and Drug Administration (FDA) has approved the first drug in a family of medicines known as JAK inhibitors that can treat myelofibrosis patients with anemia. Momelotinib (Ojjaara) is ...
Mena FN17d
Biosyngen Received Fda Approval For Phase I/Ii Clinical Trials For Brl03, Targeting Lung Cancer, Gastric Cancer And Other Advanced Solid Tumors
(MENAFN- PR Newswire) SINGAPORE, Sept. 11, 2023 /PRNewswire/ -- On September 9th, 2023, Biosyngen Pte Ltd (hereafter as "Biosyngen") announced that the U.S. FDA has cleared the Investigational New ...
The Boston Globe6d
FDA advisory panel rejects drug-device combination to treat Type 2 diabetes
A panel of medical advisers on Thursday unanimously dashed a Cambridge biotech’s hopes that US regulators would reconsider a twice-rejected implantable device designed for adults with ...
Atlanta Journal-Constitution28d
Capitol Recap: Georgia lawmakers want answers about shortage of cancer drugs
A bipartisan share of Georgia’s congressional delegation is pressing the Food and Drug Administration for information about what it’s doing to ease a shortage of cancer drugs. The shortage ...
1d
Drug companies urging FDA to block Florida prescription imports
The Food and Drug Administration is expected to soon decide if Florida can import cheaper prescription drugs from Canadian ...

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