Appeals court blocks FDA rule that allows women to obtain abortion drugs by mail

A federal appeals court temporarily reinstated a nationwide requirement that abortion pills be obtained in person, ...
Government Executive

FDA to pilot real-time clinical drug trials through cloud and AI

The first-of-its-kind pilot could lead to speedier regulatory approval of medical drugs and devices and potentially reduce ...
The Hill

FDA to weigh lifting restrictions on some MAHA-favored peptides

The Food and Drug Administration (FDA) is taking the first steps toward potentially easing access to certain peptide injections that are currently restricted due to safety concerns. The agency on ...
CNBC

FDA seeks added safety data from Lilly on newly approved weight-loss pill

The U.S. Food and Drug Administration has asked Eli Lilly for more data on liver injury linked to its newly approved obesity pill, according to a letter posted on the health regulator's website. The ...
Reuters

FDA seeks additional safety data from Lilly on newly approved weight-loss pill

April 14 (Reuters) - The U.S. Food and Drug Administration has asked Eli Lilly (LLY.N), opens new tab for more data on liver injury linked to its newly approved obesity pill, according to a letter ...
Pharm Exec

Eli Lilly Releases Updated Safety Data for Foundayo Following FDA’s Request

FDA required additional post-approval evaluation of myocardial infarction, stroke, and other cardiovascular events because approval-era data were insufficient to fully characterize risk with this new ...
STAT

FDA pushes drugmakers to report missing clinical trial results

Ed Silverman, a senior writer and Pharmalot columnist at STAT, has been covering the pharmaceutical industry for nearly three decades. He is also the author of the morning Pharmalittle newsletter and ...
Yahoo

US FDA to convene expert panel to decide on broader access to some peptides

Add Yahoo as a preferred source to see more of our stories on Google. FILE PHOTO: Signage is seen outside of the Food and Drug Administration (FDA) headquarters in White Oak, Maryland, U.S., August 29 ...
U.S. News & World Report

FDA To Review Whether To Allow More Access To Certain Peptides

FDA To Review Whether To Allow More Access To Certain Peptides By HealthDay Staff HealthDay ReporterFRIDAY, April 17, 2026 (HealthDay News) — The U.S. Food and Drug Administration (FDA) will soon ...
The Conversation

AI is reengineering drug discovery by speeding up testing and scanning petabytes of data for connections between diseases

In December, The Conversation hosted a webinar on AI’s revolutionary role in drug discovery and development. Science and technology editor Eric Smalley interviewed Jeffrey Skolnick, eminent scholar in ...
Houston Chronicle

Texas is going solo on its push for psychedelic drug treatments after private sector deal collapses

The Texas Legislature's decision last year to invest $50 million in taxpayer money on a clinical trial for the powerful hallucinogen ibogaine came amid a rising tide of enthusiasm around psychedelics.
U.S. News & World Report

New Weight Loss Pill Gets Approval But FDA Seeks More Safety Data

New Weight Loss Pill Gets Approval But FDA Seeks More Safety Data By HealthDay Staff HealthDay ReporterWEDNESDAY, April 15, 2026 (HealthDay News) — The U.S. Food and Drug Administration (FDA) has told ...