New Investigation Finds FDA's Food Side Is 'Broken' Among experts on food safety, the consensus is that the FDA's food division isn't functional. Reason · Apr 16, 2022
Noah Feldman: Will federal courts let states ban the abortion pill? Even before the Supreme Court reverses Roe v. Wade, as most court watchers expect it to do this June, the legal battle about the aftermath of the decision is getting underway. By far the most consequential aspect of the fight is likely to be about state attempts to regulate medical… Tribune News Service · Apr 16, 2022
COVID-19: First breathing test for detecting Coronavirus is authorized by FDA The Food and Drug Administration (FDA) authorized the first test, InspectIR COVID-19 Breathalyzer, to detect COVID-19 through the breath for emergency use. Full story on Dynamite News: Dynamite News · Apr 16, 2022
The FDA just approved a very quick, very accurate COVID breathalyzer test Good riddance, brain-poking swabs. Mic · Apr 15, 2022
New state laws restrict abortion pills Doctors abilities to consult patients on abortions is being further restricted by new legislation Salon · Apr 15, 2022
When mice vape, flavor matters Curiously, different JUUL flavors seemed to have different (negative) effects on mice in a novel e-cigarette study Salon · Apr 15, 2022
First COVID breath test authorized by FDA It’s a breath of fresh air. Tribune News Service · Apr 15, 2022
FDA authorizes 1st breath test for COVID-19 infection The Food and Drug Administration has issued an emergency use authorization for what it says is the first device that can detect COVID-19 in breath samples The Independent UK · Apr 14, 2022
FDA approves Covid breathalyzer that can detect cases in three minutes Device can only be operated by trained professionals The Independent UK · Apr 14, 2022
Covaxin’s Phase 2/3 clinical trials put on hold in the US HYDERABAD: The US Food and Drug Administration has put on hold the phase 2/3 clinical trials of Bharat Biotech’s Covid-19 vaccine Covaxin in the US. The Times of India · Apr 14, 2022
Baby formula shortage: What is causing supply issue and which stores are rationing products? Out-of-stock per centages reached higher than 40 per cent in seven states in first week of April The Independent UK · Apr 14, 2022
Covaxin trials in U.S. put on hold WHO had announced suspension of the vaccine supplies through UN procurement agencies The Hindu · Apr 14, 2022
Magenta Therapeutics Trims R&D, Cuts Workforce Magenta Therapeutics Inc (NASDAQ:MGTA) is cutting 14% of staff and axing a planned dosing optimization trial for a stem cell mobilization med, focused on extending its cash runway into Q2 2024. The cost-saving measures focus on shaving administrative expenses and new research investments, including the Company's planned dosing and administration optimization trial… Benzinga · Apr 14, 2022
Adagio Pauses FDA Emergency Use Request For Its COVID-19 Therapy Adagio Therapeutics Inc (NASDAQ:ADGI) provided an update on the anticipated timing for its Emergency Use Authorization (EUA) request for adintrevimab (ADG20) for the prevention and treatment of COVID-19. Adintrevimab has demonstrated broadly neutralizing activity in vitro against variants of concern, including Alpha, Beta, Delta, Delta Plus, Gamma, and Omicron BA.1. But, the candidate has markedly… Benzinga · Apr 14, 2022
The Independent UK · Apr 14, 2022 E-cigs using synthetic nicotine come under FDA oversight The Food and Drug Administration says it will begin cracking down on e-cigarettes that have used synthetic nicotine to skirt oversight
Benzinga · Apr 14, 2022 Why Lexaria Shares Are Rising Today Lexaria Bioscience Corp (NASDAQ:LEXX) said that all data analyses from its simulated pulmonary hypertension clinical study HYPER-H21-3 are complete, assessing a single 300mg dose of DehydraTECH-processed cannabidiol (DehydraTECH-CBD). The study findings indicated a tendency (p=0.1) during 15 minutes of simulated low levels of oxygen (hypoxia) for reduced pulmonary artery systolic pressure (PASP)…
Benzinga · Apr 14, 2022 The Daily Biotech Pulse: Pfizer-BioNTech COVID-19 Booster Data In Kids, Regeneron's COVID-19 Therapy Decision Pushed, Protagonist's Rusfertide Breakthrough Tag Update And More Here's a roundup of top developments in the biotech space over the last 24 hours:
Benzinga · Apr 14, 2022 FDA Extends Review Period For Regeneron's COVID-19 Antibody Therapy The FDA has extended its review of Regeneron Pharmaceuticals Inc's (NASDAQ:REGN) marketing application of REGEN-COV (casirivimab and imdevimab) for non-hospitalized COVID-19 patients and as prophylaxis in certain individuals. The extension is due to ongoing discussions with the FDA on pre-exposure prophylactic use. Regeneron has submitted additional data from its completed prophylaxis trial that the…
The Conversation · Apr 14, 2022 The FDA approved a new drug to treat Alzheimer's, but Medicare won't always pay for it – a doctor explains what researchers know about Biogen's Aduhelm Medicare finalized its decision to restrict its coverage of Aduhelm, Biogen’s new Alzheimer’s disease drug, on April 8, 2022.
Benzinga · Apr 14, 2022 FDA Intends To Revoke Protagonist Therapeutics' Rusfertide Breakthrough Tag In Rare Form Of Blood Cancer Protagonist Therapeutics Inc (NASDAQ: PTGX)
Tribune News Service · Apr 14, 2022 Outlook poses tough questions for next steps on COVID-19 vaccines Preparations for another potential round of COVID-19 vaccines are prompting more questions than answers as federal health officials contend with the threat of future variants amid waning public interest in additional shots.
Chicago Tribune · Apr 13, 2022 New type of cigarette that ‘helps you smoke less’ debuts in Chicago stores this week, amid some controversy Cigarettes that recently gained authorization from the Food and Drug Administration to be marketed as products that can help smokers cut back are hitting Chicago-area stores this week — the first place in the country where they will be sold.
Reason · Apr 13, 2022 The FDA's Rejection of a Major Vaping Brand Shows It Is Arbitrarily Applying a Nebulous Legal Standard The agency's obsession with adolescent vaping is driving decisions that undermine public health.
Benzinga · Apr 13, 2022 Read Why Pliant Therapeutics Shares Are Soaring Today Pliant Therapeutics Inc (NASDAQ: PLRX) says that with just two FDA-approved Idiopathic Pulmonary Fibrosis drugs, it believes that is a high unmet need.