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Food and Drug Administration (FDA) to detain GLP-1 APIs manufactured at foreign facilities not approved by the agency

Akston Biosciences is sponsoring a Cornell University clinical study of a once-weekly GLP-1 therapy for overweight and obese cats, while San Francisco-based OKAVA Pharmaceuticals has begun testing a long-acting implant designed to deliver the medicine continuously for up to six months

The Future of GLP-1 Therapy: Individualized Care The GLP-1 revolution marks a new chapter in personalized medicine

The BRAAFF checklist: A new dermoscopic algorithm for diagnosing acral melanoma

Advertisement This protocol is an extension of the widely accepted PEN-FAST (penicillin allergy reported by patient, five years or less since reaction, anaphylaxis or angioedema, severe cutaneous adverse reaction, and treatment required for reaction) clinical decision tool that has been used to identify patients with reported penicillin allergy who are appropriate for DOC rather than immediate hypersensitivity skin testing, which recent data suggest has poor positive predictive value in low-risk patients