UK's MHRA the first regulator to approve Pfizer's Cibinqo

14 September 2021
pfizer_colour_new_large

The UK Medicines and Healthcare products Regulatory Agency (MHRA) has granted marketing authorization in Great Britain for Cibinqo (abrocitinib), an oral, once-daily, Janus kinase 1 (JAK1) inhibitor.

Developed by US pharma giant Pfizer (NYSE: PFE), Cibinqo is approved for the treatment of moderate to severe atopic dermatitis (AD) in adults and adolescents aged 12 years and over, who are candidates for systemic therapy. Abrocitinib is licensed in recommended doses of 100mg and 200mg.

This is the first marketing authorization in the world for this treatment, Pfizer noted.

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK

Today's issue

Company Spotlight





More Features in Biotechnology