The primary hypothesis is that the co-formulation of guselkumab and golimumab (JNJ-78934804) is superior to both guselkumab and golimumab alone as measured by clinical remission at Week 48 for the treatment of participants with moderately to severely active UC who have had an inadequate initial response, loss of response, or intolerance to ≥1 ADT (defined as a biologic or a novel oral agent with biologic-like activity).
Thank you for your interest, but this study is recruiting by invitation only.
North Carolina (Statewide)
Animesh Jain
Medicine-Gastroenterology
Clinical or Medical
Interventional
Stomach, Digestion and Gut Health
22-3020