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
概览
- 阶段
- 2 期
- 干预措施
- JNJ-78934804
- 疾病 / 适应症
- Crohn's Disease
- 发起方
- Janssen Research & Development, LLC
- 入组人数
- 703
- 试验地点
- 801
- 主要终点
- Percentage of Participants with Clinical Remission at Week 48
- 状态
- 进行中（未招募）
- 最后更新
- 19天前
概览
简要总结
The purpose of this study is to evaluate the efficacy of JNJ-78934804 at Week 48 compared to guselkumab and golimumab.
研究者
入排标准
入选标准
- •Diagnosis of Crohn's disease (CD) for at least 3 months prior to baseline
- •Confirmed diagnosis of moderate to severe CD as assessed by Crohn'
排除标准
- 未提供
研究组 & 干预措施
Group 5: JNJ-78934804 (Mid-dose)
Participants will receive JNJ-78934804 dose regimen 2 SC. All participants who meet inadequate response criteria will be escalated to an active treatment. Participants who are eligible and willing to continue the study intervention that they are receiving at Week 44 may enter the long-term extension.
干预措施: JNJ-78934804
Group 6: JNJ-78934804 (Low-dose)
Participants will receive JNJ-78934804 dose regimen 3 SC. All participants who meet inadequate response criteria will be escalated to an active treatment. Participants who are eligible and willing to continue the study intervention that they are receiving at Week 44 may enter the long-term extension.
干预措施: JNJ-78934804
Group 1: Placebo
Participants will receive placebo subcutaneously (SC). All participants who meet inadequate response criteria will be escalated to an active treatment. Participants who are eligible and willing to continue the study intervention that they are receiving at Week 44 may enter the long-term extension.
干预措施: Placebo
Group 4: JNJ-78934804 (High-dose)
Participants will receive JNJ-78934804 dose regimen 1 SC. All participants who meet inadequate response criteria will be escalated to an active treatment. Participants who are eligible and willing to continue the study intervention that they are receiving at Week 44 may enter the long-term extension.
干预措施: JNJ-78934804
Group 2: Guselkumab
Participants will receive guselkumab dose regimen 1 SC. All participants who meet inadequate response criteria will be escalated to an active treatment. Participants who are eligible and willing to continue the study intervention that they are receiving at Week 44 may enter the long-term extension.
干预措施: Guselkumab
Group 3: Golimumab
Participants will receive golimumab dose regimen 1 SC. All participants who meet inadequate response criteria will be escalated to an active treatment. Participants who are eligible and willing to continue the study intervention that they are receiving at Week 44 may enter the long-term extension.
干预措施: Golimumab
结局指标
主要结局
Percentage of Participants with Clinical Remission at Week 48
时间窗: Week 48
Percentage of participants with clinical remission at Week 48 will be reported. Clinical remission is based on the Crohn's Disease Activity Index (CDAI).
Percentage of Participants with Endoscopic Response at Week 48
时间窗: Week 48
Percentage of participants with endoscopic response at Week 48 will be reported. Endoscopic response is based on change from baseline in the simple endoscopic score for Crohn's disease (SES-CD), as assessed by central endoscopy reading.
次要结局
- Percentage of Participants with Endoscopic Remission at Week 48(Week 48)
- Percentage of Participants with Patient-reported Outcomes (PRO)-2 Remission at Week 48(Week 48)
- Percentage of Participants with Corticosteroid-Free Clinical Remission at Week 48(Week 48)
- Secondary Comparison: Percentage of Participants with Clinical Remission at Week 48(Week 48)
- Secondary Comparison: Percentage of Participants with Endoscopic Response at Week 48(Week 48)
- Percentage of Participants with Adverse Events (AEs)(Up to Week 48)
- Percentage of Participants with Serious Adverse Events (SAEs)(Up to Week 48)
- Clinical Laboratory Parameters Over Time(Up to Week 48)
- Vital Sign Parameters Over Time(Up to Week 48)
- Suicidal Ideation Assessment Using Columbia Suicide Severity Rating Scale (C-SSRS) Score(Up to Week 48)
- Serum Concentrations of Guselkumab Over Time(Up to Week 48)
- Serum Concentrations of Golimumab Over Time(Up to Week 48)
- Percentage of Participants with Antibodies to Guselkumab(Up to Week 48)
- Titers of Antibodies to Guselkumab(Up to Week 48)
- Percentage of Participants with Antibodies to Golimumab(Up to Week 48)
- Titers of Antibodies to Golimumab(Up to Week 48)
- Percentage of Participants with Neutralizing Antibodies to Guselkumab.(Up to Week 48)
- Percentage of Participants with Neutralizing Antibodies to Golimumab(Up to Week 48)