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Health Care Roundup: Market Talk
The Wall Street Journal· 13 hours agoAn FDA decision on whether to approve donanemab as a competitor to Leqembi from Eisai and Biogen had been expected in the first quarter, but the agency...
FDA rescinds ban on Juul e-cigarettes
Medical Xpress· 18 hours agoWhile the company's e-cigarettes are back under review, they have not been fully cleared for sale in this country, the FDA said in its announcement. Juul...
Eli Lilly Is Trading At A Record High Ahead Of A Key FDA Meeting — Is It A Buy?
Investor's Business Daily· 16 hours agoLilly is also planning to ask the FDA to approve tirzepatide in patients with obstructive sleep...
US FDA expands GSK’s RSV vaccine approval to adults aged 50 to 59
WSAU Wausau· 11 hours agoBy Sriparna Roy and Christy Santhosh (Reuters) -The U.S. Food and Drug Administration approved the...
Telomerase Inhibitor Approved for MDS-Related Anemia
MedPage Today· 1 day agoThe FDA approved imetelstat (Rytelo) for adults with low- to intermediate-1 risk myelodysplastic syndromes (MDS) with transfusion-dependent anemia who...
FDA advisors express skepticism as they debate MDMA therapy for PTSD
WUSF 89.7· 4 days agoTuesday, scientific advisors to the Food and Drug Administration are deciding whether to recommend...
Intuitive Surgical (ISRG) Gets FDA Nod for da Vinci's New Label
Zacks via Yahoo Finance· 18 hours agoThe da Vinci portfolio currently includes seven approved systems, which are the da Vinci standard...
Geron Shares Surge After U.S. FDA Approves Blood Disorder Drug
US News & World Report· 24 hours agoCalifornia-based Geron said it will discuss the new drug's pricing and availability in a conference call with investors later in the day. Rytelo is approved for the treatment ...
Geron shares surge after U.S. FDA approves blood disorder drug
WSAU Wausau· 24 hours ago(Reuters) - Shares of Geron rose almost 16% on Friday before market, a day after getting its first...
FDA Platform Technology Designation Program aims to speed development of drugs, biological products...
JD Supra· 4 days agoFDA developed the new platform technology designation program draft guidance to fulfill its requirement under Section 506K(b) of the Federal Food, Drug, and Cosmetic Act ( ...
