News

Mind Medicine: Initiating Hold Rating Due To Regulatory Challenges
Regulatory delays could hinder Mind Medicine's patient access and market entry. Read why we are initiating coverage on MNMD ...
Denver713d
'It saved my life': Patient, psychiatrist believe ketamine therapy is integral in changing trauma responses
Ketamine is only approved by the FDA as an anesthetic, but there is growing interest in using ketamine products to treat ...
Medical Xpress15d
Treatment-resistant depression responds better to esketamine with SNRI than SSRI, study finds
Esketamine nasal spray, a rapid-acting anti-depressant, is known to be effective against TRD when administered alongside antidepressants like selective serotonin reuptake inhibitor (SSRI ...
Medscape19d
Esketamine Combo Bests SSRIs for Resistant Depression in Head-to-Head Trial
Esketamine combined with a serotonin-norepinephrine reuptake inhibitor (SNRI) for treatment-resistant depression (TRD) was linked to significantly lower rates of several adverse outcomes than ...
The Grand Junction Daily Sentinel19d
FDA Delays Final Approval of Novavax COVID Vaccine
FRIDAY, April 4, 2025 (HealthDay News) -- The U.S. Food and Drug Administration (FDA) has delayed the full approval of Novavax’s COVID-19 vaccine. The decision had been expected by April 1 ...
Reuters21d
US Supreme Court largely backs FDA's denial of flavored vape product applications
The justices threw out a lower court's decision that the FDA had failed to follow proper legal procedures under a federal law called the Administrative Procedure Act when it rejected the ...
Business Insider24d
FDA recalls over 4,000 bags of ground coffee mislabeled as decaffeinated across 15 states
The FDA recalled over 4,000 bags of ground coffee mislabeled as decaffeinated across 15 states. The recall applies to 12-ounce bags of Our Family's Traverse City Cherry Decaf Light Roast.
New York Post25d
Top vaccine official resigns from FDA, criticizes RFK Jr.
Dr. Peter Marks sent a letter to Acting FDA Commissioner Sara Brenner on Friday saying that he would resign and retire by April 5 as director of the Center for Biologics Evaluation and Research.
Los Angeles Times25d
Top FDA vaccine official resigns, criticizes Kennedy for promoting ‘misinformation and lies’
Dr. Peter Marks sent a letter to acting FDA Commissioner Sara Brenner on Friday saying that he would resign and retire by April 5 as director of the Center for Biologics Evaluation and Research.
People25d
FDA's Top Vaccine Scientist Resigns Due to Robert F. Kennedy Jr.'s 'Misinformation and Lies'
Greg Nash/The Hill/Bloomberg via Getty; Kevin Dietsch/Getty Dr. Peter Marks, one of the U.S. Food and Drug Administration’s (FDA) top vaccine officials, has resigned. In a resignation letter ...
MSNBC25d
The FDA’s top vaccine official resigns, pointing to Kennedy’s ‘misinformation and lies’
Dr. Peter Marks, who oversaw the FDA’s vaccine division as director of the Center for Biologics Evaluation and Research, submitted his resignation to acting FDA Commissioner Sara Brenner on Friday.
The Independent25d
Top FDA vaccine expert blasts RFK Jr. as he’s forced out
Dr Peter Marks, the director for the agency’s Center for Biologics Evaluation and Research, submitted his resignation letter to FDA Acting Commissioner Sara Brenner, citing Health and Human ...