Bristol's High Profile TYK2 Inhibitor Disappoints In Ulcerative Colitis

Deucravacitinib is an oral drug in development for a wide range of autoimmune conditions, including psoriasis and psoriatic arthritis.

Time out hands
Bristol's TYK2 inhibitor failed a Phase II study in ulcerative colitis • Source: Alamy

Bristol Myers Squibb Company has ambitious development plans for its first-in-class selective tyrosine kinase 2 (TYK2) inhibitor deucravacitinib in a wide range of autoimmune diseases, but one proof-of-concept study has come up short. The company announced on 7 October that a Phase II trial testing deucravacitinib in ulcerative colitis failed to meet the primary efficacy endpoint of clinical remission at Week 12, and missed the secondary efficacy endpoints, including clinical response, endoscopic response and histological improvement at Week 12.

The news raises some concern about the broad potential of deucravacitinib in a wide range of diseases, particularly in inflammatory bowel diseases, where BMS has been looking to develop the drug for ulcerative colitis and Crohn's disease. The company is hoping to build out a gastrointestinal disease franchise, starting with Zeposia (ozanimod), which was recently approved for ulcerative colitis

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 Immunological

Merck & Co. CMO Barr On Breaking Into Immunology And Ophthalmology

 

Chief medical officer Eliav Barr discussed Merck’s investment in new therapeutic areas and business development in an interview with Scrip.

J&J’s Imaavy Approval Is The Starting Line For Pipeline-In-A-Product Strategy

 

The company’s FcRn inhibitor nipocalimab was approved by the US FDA for generalized myasthenia gravis (gMG), where it will join a competitive market.

In Brief: AbbVie’s Rinvoq Secures US Approval For Giant Cell Arteritis

 

JAK inhibitor gains ninth indication in US after a strong performance in the first quarter.

EU Approves Tremfya In Third Indication, Ulcerative Colitis

 

J&J secures EU approval for its IL-23 inhibitor Tremfya for ulcerative colitis, its third indication in the region, amid strong competition in the sector. EU approval is also awaited for Crohn’s disease.

More from Therapy Areas

Lilly And Alchemab Tap Into Resilient Individuals To Develop ALS Drug

 

The pharma company is helping to validate the biotech’s model by developing a novel amyotrophic lateral sclerosis candidate, based on its novel approach that ‘turns drug discovery on its head’.

BioNTech Aims To Diversify BNT323 Manufacturing As Filing Nears

 

The company plans to expand manufacturing of the HER2-targeting ADC beyond China and plans to file for US FDA approval in 2025.

Accelerated Approval May Be Out Of Reach For PTC’s Huntington’s Drug

 
• By 

PTC said its updated Phase II data for PTC 518 met the primary endpoint of Huntingtin’s protein reduction, but analysts said there isn’t clear correlation with clinical benefit.