Tulisokibart

Drug

Drug Profile

Tulisokibart (MK-7240) is an investigational humanized anti-TL1A monoclonal antibody in development for immune-mediated inflammatory diseases. Merck reports ongoing Phase 3 programs in ulcerative colitis and Crohn's disease, with additional Phase 2b trials in hidradenitis suppurativa, radiographic axial spondyloarthritis, and rheumatoid arthritis. It has no marketing approval.

Drug Class
Investigational humanized anti-TL1A monoclonal antibody
Approval Status
Investigational (in Phase 3/2b clinical trials; no regulatory approval)
Mechanism of Action
Binds both soluble and membrane-bound human TL1A and may inhibit inflammatory pathways and intestinal fibrosis.
Indications
  • \Ulcerative colitis (investigational)\
  • \Crohn's disease (investigational)\
  • \Systemic sclerosis-associated interstitial lung disease (investigational)\
  • \Hidradenitis suppurativa (investigational)\
  • \Radiographic axial spondyloarthritis (investigational)\
  • \Rheumatoid arthritis (investigational)\

Related News

Related Clinical Trials

NCT ID Title Status Phase
NCT07486960

Study to Evaluate Tulisokibart in Adults With Psoriatic Arthritis (MK-7240-015)

RECRUITING PHASE2
NCT07176390

A Clinical Study of Tulisokibart (MK-7240) to Treat Rheumatoid Arthritis (RA) (MK-7240-014)

RECRUITING PHASE2
NCT07133633

A Clinical Study of Tulisokibart (MK-7240) to Treat Radiographic Axial Spondyloarthritis (MK-7240-013)

RECRUITING PHASE2
NCT06956235

Study to Evaluate Tulisokibart for Hidradenitis Suppurativa (MK-7240-012)

ACTIVE_NOT_RECRUITING PHASE2
NCT06829225

Single Dose Study of Tulisokibart (MK-7240) in Healthy Chinese Participants (MK-7240-002)

COMPLETED PHASE1
NCT06651281

Extension Study of Long-term Safety and Efficacy of Tulisokibart in Participants With Crohn's Disease or Ulcerative Colitis (MK-7240-011)

RECRUITING PHASE3
NCT06575595

Pharmacokinetic (PK) Characterization of Subcutaneous Tulisokibart (MK-7240-010)

COMPLETED PHASE1
NCT05270668

Phase 2 Safety and Efficacy Study of Tulisokibart (MK-7240/PRA023) in Subjects With Systemic Sclerosis Associated With Interstitial Lung Disease (SSc-ILD) (MK-7240-007)

ACTIVE_NOT_RECRUITING PHASE2
NCT05013905

A Phase 2a Safety and Efficacy Open-Label Study of Tulisokibart (MK-7240/PRA023) in Participants With Moderately to Severely Active Crohn's Disease (MK-7240-006)

COMPLETED PHASE2
NCT04996797

A Phase 2 Safety and Efficacy Study of Tulisokibart (MK-7240/PRA023) in Subjects With Moderately to Severely Active Ulcerative Colitis (MK-7240-005)

COMPLETED PHASE2