Skip to main content

golimumab

Generic: golimumab·Brand: Simponi

golimumab: 4 clinical trials tracked.

golimumab evidence translation

What we can confirm

4 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about golimumab, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 1 study sponsors

Related indications

Clinical Trials (4)

A Phase 2b Randomized, Double-blind, Active-and Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of Induction and Maintenance Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Ulcerative Colitis

NCT05242484·Phase 2·GHRS
Active, not recruiting

Primary endpoint: Percentage of Participants with Clinical Remission at Week 48

InterventionalRandomizeddouble577 enrolledStarted 2022-09Completion 2029-0350 sites · United StatesJanssen Research & Development, LLC

A Phase 2b Randomized, Double-blind, Active-and Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of Induction and Maintenance Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Crohn's Disease

NCT05242471·Phase 2·GHRS
Active, not recruiting

Primary endpoint: Percentage of Participants with Clinical Remission at Week 48

InterventionalRandomizeddouble703 enrolledStarted 2022-07Completion 2029-1150 sites · United StatesJanssen Research & Development, LLC

A Phase 2a, Multicenter, Randomized, Double-blind Study Evaluating the Efficacy and Safety of Subcutaneously Administered Guselkumab and Golimumab Combination Therapy in Participants With Active Psoriatic Arthritis

NCT05071664·Phase 2·GHRS
Completed

Primary endpoint: Percentage of Participants Who Achieved Minimal Disease Activity (MDA) at Week 24

InterventionalRandomizeddouble91 enrolledStarted 2021-10Completion 2024-0850 sites · Denmark, France, Hungary, Italy…Janssen Research & Development, LLC

A Phase 3 Randomized, Open-Label Study to Assess the Efficacy, Safety, and Pharmacokinetics of Golimumab Treatment, a Human Anti-TNFα Monoclonal Antibody, Administered Subcutaneously in Pediatric Participants With Moderately to Severely Active Ulcerative Colitis

NCT03596645·Phase 3·GHRS
Active, not recruiting

Primary endpoint: Percentage of Participants With Clinical Remission at Week 6 as Assessed by the Mayo Score

InterventionalRandomizedopen84 targetStarted 2018-10Completion 2027-0250 sites · Belgium, Brazil, France, Israel…Janssen Research & Development, LLC