Severe cases of the bleeding disorder can be life-threatening. The U.S. Food and Drug Administration (FDA) has granted approval for Roctavian, gene therapy for adults with severe hemophilia…
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FTC and FDA Warn Companies Selling Copycat Delta-8 THC
The joint effort by federal agencies seeks to protect consumers from the potentially harmful ingredient. The Federal Trade Commissioner (FTC) and the Food and Drug Administration (FDA) have…
Read MoreFDA Fully Approves Alzheimer’s Drug Leqembi
This traditional approval follows previously fast-tracked authorization. The Food and Drug Administration (FDA) has approved Leqembi for the treatment of Alzheimer’s disease. The FDA included a safety warning…
Read MoreEnergy Department Awards Grants for School Facilities
Funding program supports energy upgrades for institutions in impoverished communities. The Department of Energy (DOE) recently announced the first round of selections for their Renew America’s Schools grant…
Read MoreCDC Recommends RSV Vaccine for Seniors
HHS secretary commends the approval. The Centers for Disease Control and Prevention (CDC) recently announced the recommendation for the Respiratory Syncytial Virus (RSV) vaccine for seniors 60 and…
Read MoreFDA Approves First Cell Therapy for Type 1 Diabetes
The treatment was developed to address patients struggling to maintain target blood glucose levels. The U.S. Food and Drug Administration recently granted approval to CellTrans, Inc. for Lantidra.…
Read MoreVA Report Shows Opioid Treatment Program Failing Veterans
Office of Inspector General report exposes general oversights in the VA healthcare system. The Office of Inspector General within the Department of Veterans Affairs has reported that healthcare…
Read MoreWhite House Acknowledges President’s Sleep Apnea
Journalist questions marks on the president’s face from the use of a C-PAP machine. White House officials said Wednesday that President Joe Biden has begun using a continuous…
Read MoreFDA Approves Gene Therapy for Muscular Dystrophy in Children
Treatment is intended for kids with a confirmed mutation of the DMD gene. The U.S. Food and Drug Administration (FDA) recently approved Elevidys, the first gene therapy for…
Read MoreU.S. Military Adds Blue Lotus to Banned Substance List
FDA does not regulate the psychotropic drug, available via e-cigarettes or vaping. The Department of Defense has added blue lotus, a drug from the Egyptian flower Nymphaea caerulea,…
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