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Even as the US Food and Drug Administration (FDA) has unveiled a strategic expansion of its oversight mechanisms for foreign ...
The US regulator has cleared use of Kerendia (finerenone) for the treatment of heart failure patients who have a left ...
Bravecto Quantum is the first FDA-approved drug that treats and prevents flea and tick infestations on dogs for a duration of ...
Takeda is on track to submit its much-hyped narcolepsy drug to regulators this fiscal year after the orexin receptor 2 (OX2R)-selective agonist ...
Collection of ethnicity data in clinical research has been poor historically, but is essential to ensure that interventions are effective and safe across diverse populations. These data are needed to ...
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Vietnam Investment Review on MSNImugene Reports Strong Results for Azer cel in DLBCL TrialImugene Limited (ASX: IMU), a clinical-stage immuno-oncology company, is pleased to announce exciting new data from its Phase 1b clinical trial evaluating azer-cel (azercabtagene zapreleucel) in ...
FDA Commissioner Marty Makary's vision for the agency risks the best of an agency that mostly has functioned well for the ...
Managed Healthcare Executive gives C-suite executives in health plans and provider organizations news and strategies for value-driven solutions.
Atrioventricular interval modulation is being studied for patients with uncontrolled hypertension. Could the new technology ...
British drugmaker GSK said on Monday it had submitted an application to the U.S. Food and Drug Administration to extend the ...
The company expects to make the updated Spikevax available to U.S. patients in time for the 2025-26 respiratory virus season.
People with a nut allergy or severe sensitivity to hazelnuts run the risk of serious or life-threatening allergic reactions,” ...
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