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Clinical Trials List

Protocol Number78934804UCO2001
NCT Number(ClinicalTrials.gov Identfier)NCT05242484
Active

2022-11-30 - 2028-12-31

Phase II

Not yet recruiting5

Recruiting1

ICD-10K51.90

Ulcerative colitis, unspecified, without complications

ICD-10K51.911

Ulcerative colitis, unspecified with rectal bleeding

ICD-10K51.912

Ulcerative colitis, unspecified with intestinal obstruction

ICD-10K51.913

Ulcerative colitis, unspecified with fistula

ICD-10K51.914

Ulcerative colitis, unspecified with abscess

ICD-10K51.918

Ulcerative colitis, unspecified with other complication

ICD-10K51.919

Ulcerative colitis, unspecified with unspecified complications

ICD-9556.9

Ulcerative colitis, unspecified

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

  • Trial Applicant

    PAREXEL INTERNATIONAL CO., LTD.

  • Sponsor

  • Trial scale

    Multi-Regional Multi-Center

  • Update

    2026/02/01

Investigators and Locations

Principal Investigator SHU-CHEN WEI Division of General Internal Medicine

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Not yet recruiting

Principal Investigator 顏旭亨 Division of General Internal Medicine

Co-Principal Investigator

  • 吳東龍 Division of General Internal Medicine
  • 張譽耀 Division of General Internal Medicine
  • 楊承達 Division of General Internal Medicine

The Actual Total Number of Participants Enrolled

0 Not yet recruiting

Principal Investigator Jen-Wei Chou Digestive System Department

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Not yet recruiting

Principal Investigator CHUNG-HSIN CHANG Division of General Internal Medicine

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Not yet recruiting

Principal Investigator Cheng-Tang Chiu Digestive System Department

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator Chiao-Hsiung Chuang Division of General Internal Medicine

Co-Principal Investigator

  • 康瑞文 Division of General Internal Medicine
  • 陳柏潤 Division of General Internal Medicine

The Actual Total Number of Participants Enrolled

0 Not yet recruiting

Condition/Disease

Colitis, Ulcerative

Objectives

Main Purpose: JNJ-78934804 was evaluated at week 48 compared with various monotherapies (guselkumab alone and golimumab alone) Secondary Purpose: ‧ Evaluate the efficacy of JNJ-78934804 compared with various monotherapies on various outcome measures ‧ Evaluate the efficacy of JNJ-78934804 compared with placebo at week 24 ‧ Evaluate the safety of JNJ-78934804 compared with various monotherapies and placebo ‧ Evaluate the pharmacokinetics (PK) and immunogenicity of JNJ-78934804 compared to various monotherapies

Test Drug

GuselkumabGolimumabJNJ-78934804

Active Ingredient

Guselkumab
Golimumab
Guselkumab and Golimumab co-formulation

Dosage Form

Prefilled syringe with UltraSafe Plus
Prefilled syringe with UltraSafe
Prefilled syringe with UltraSafe Plus

Dosage

100 mg/mL
100 mg/mL
100mg Guselkumab and 100mg Golimumab/2mL

Endpoints

The percentage of participants in clinical remission at Week 48 will be reported. Clinical remission was based on the modified Mayo subscore.

Inclution Criteria

Inclusion Criteria:

Confirmed diagnosis of ulcerative colitis (UC) for at least 3 months prior to baseline
Moderately to severely active UC as assessed by the modified Mayo score
Demonstrated inadequate response, loss of response, or intolerance to at least one biologic or novel oral with biologic-like activity
If female and of childbearing potential, must meet the contraception and reproduction requirements

Exclusion Criteria

Exclusion Criteria:

Has severe extensive colitis as defined in the protocol
Extent of inflammatory disease limited to the rectum
Participants with current diagnosis of indeterminate colitis, microscopic colitis, ischemic colitis, or Crohn's disease (CD)
Has a history of, or ongoing, chronic or recurrent infectious disease, including but not limited to, sinopulmonary infections, bronchiectasis, recurrent renal/urinary tract infections (example, pyelonephritis, cystitis), an open, draining, or infected skin wound, or an ulcer
Currently has a malignancy or a history of malignancy within 5 years before screening (with the exception of nonmelanoma skin cancer or cervical carcinoma in situ that has been treated with no evidence of recurrence within 12 months of first dose of study intervention)

The Estimated Number of Participants

  • Taiwan

    6 participants

  • Global

    550 participants