AbbVie’s Skyrizi Checks One Last Box With Phase III Success In Ulcerative Colitis

UC Is Final Planned Indication For IL-23 Inhibitor

Already approved in Crohn’s disease, Skyrizi now has positive Phase III results in ulcerative colitis with more data expected this year in UC as the field grows more crowded with anti-IL-23 options.

Check marks on four wooden blocks
Ulcerative colitis is the fourth and final indication for Skyrizi • Source: Shutterstock

AbbVie Inc.’s IL-23 inhibitor Skyrizi (risankizumab) delivered its first set of positive Phase III results in ulcerative colitis (UC) on 23 March from INSPIRE, a 12-week induction study, and the company plans to report data from Phase III COMMAND clinical trial, a 52-week maintenance study, during the first half of 2023. Positive results from both trials will position the product for regulatory filings later this year and a launch in UC – an increasingly crowded market, particularly for IL-23 inhibitors – in 2024.

Skyrizi already is approved in the US, EU and several other markets for Crohn’s disease, giving the product a foothold...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Clinical Trials

More from R&D

Investors Back Nuclidium’s Next-Gen Copper-Based Radiopharmaceuticals

 

The Swiss company believes its platform can make radiopharmaceuticals easier to produce and more accessible to patients.

Lupin’s Cimzia Biosimilar Candidate Reflects Strategy To Separate Wheat From Chaff

 
• By 

Lupin's choice of a Cimzia biosimilar candidate and partnering with Zentiva reflect a strategy to sort the wheat from the chaff. Of 118 biologics to lose patent protection between 2025 and 2034 as per IQVIA, it’s going for a biosimilar with a single competitor though there could be other spoilers

Taiho’s Oral, Mutation-Agnostic DMD Candidate Misses Phase III Endpoint

 
• By 

The oral, twice-daily candidate was expected to control decline in motor function in DMD patients regardless of their gene mutations.