Company scheduled to meet with the FDA in mid-April 2026 to review the results of the Phase 3 EFZO-FIT study and determine the path forward for efzofitimod in pulmonary sarcoidosis. Phase 2 EFZO-CONNE ...
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Lead found in everyday vegetables: Bengaluru study raises serious food safety concerns
A recent investigation in Bengaluru has raised fresh concerns about food safety. Tests found dangerous levels of lead in ...
During a live event, Joshua Richter, MD, explored proactive adverse event management when using selinexor in multiple myeloma. At a live Case-Based Roundtable event during the 2025 American Society of ...
Accelerated review was enabled by the Commissioner’s National Priority Voucher Pilot Program, targeting high unmet need and compressing FDA action to 1–2 months with enhanced reviewer communication.
In the Phase 2/3 COMPANION-002 study of tovecimig (DLL4 x VEGF-A bispecific antibody) in patients with biliary tract cancer, the prespecified ...
The FDA has put a partial clinical hold on PepGen’s phase 2 mus | The FDA has put a partial clinical hold on PepGen’s phase 2 muscle wasting trial after reviewing preclinical data, continuing the stop ...
Here's a list of luxury MPVs that can offer a celebrity like feel to the owner, the list includes models from brands like Toyota, Mercedes-Benz, and others.
PepGen said on Wednesday that the U.S. Food and Drug Administration has placed a partial clinical ​hold on its mid‑stage trial of a rare ‌muscle disease drug, sending its shares plunging over 25% in ...
Sleeping for 7 hours and 18 minutes every night may be the sweet spot for warding off the risk of insulin resistance-the precursor to type 2 diabetes-suggests a large observational study published in ...
AB Science says a newly identified blood biomarker may help assess masitinib activity in its ongoing Phase 3 ALS clinical ...
According to GAC, the technology's high energy density and safety address the limitations of conventional liquid batteries, improving electric vehicles' range and safety. Liquid batteries are the most ...
Novo Nordisk today announced that the US Food and Drug Administration (FDA) has approved three new indications for once-weekly Sogroya (R) (somapacitan-beco) injection 5 mg, 10 mg, or 15 mg, a ...
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