Peptide News Digest

#MHRA

5 stories

MHRA — the UK Medicines and Healthcare products Regulatory Agency — is the European-side counterpart most actively covered on this site. The agency has been visible on research-peptide enforcement, NHS coverage decisions for branded GLP-1s, and the broader UK aesthetic-medicine market.

Recent threads: MHRA warning letters and product seizures targeting peptide vendors selling BPC-157, TB-500, and other research peptides; updates on UK telehealth GLP-1 prescribing; and the agency's coordination with Trading Standards on online sale of unapproved peptides.

Stories here cover MHRA actions, NHS coverage, and UK enforcement. See #uk for the broader UK thread and #uk-regulation for related rule-making.

Regulatory · View digest

UK MHRA Approves Wegovy Pill (Oral Semaglutide 25 mg) for Chronic Weight Management

Novo Nordisk announced on June 11 that the UK Medicines and Healthcare products Regulatory Agency had approved the Wegovy pill (oral semaglutide tablets 25 mg) for adults with obesity (BMI ≥30) or overweight (BMI ≥27) with at least one weight-related comorbidity, making the UK the third national authority to license the molecule after the FDA and the UAE's EDE. The approval rests on the Phase 3 OASIS 4 trial, which showed about 13.6% weight loss with the 25 mg tablet versus 2% on placebo. Private-prescription availability is expected within weeks; NHS coverage requires a separate NICE cost-effectiveness appraisal.