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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT05242471




Registration number
NCT05242471
Ethics application status
Date submitted
15/02/2022
Date registered
16/02/2022
Date last updated
22/05/2024

Titles & IDs
Public title
A Study of Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Crohn's Disease
Scientific title
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
Secondary ID [1] 0 0
2021-003314-39
Secondary ID [2] 0 0
CR109178
Universal Trial Number (UTN)
Trial acronym
DUET-CD
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Crohn's Disease 0 0
Condition category
Condition code
Oral and Gastrointestinal 0 0 0 0
Inflammatory bowel disease
Inflammatory and Immune System 0 0 0 0
Other inflammatory or immune system disorders
Oral and Gastrointestinal 0 0 0 0
Crohn's disease

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Other interventions - Guselkumab
Other interventions - Golimumab
Other interventions - JNJ-78934804
Treatment: Drugs - Placebo

Placebo Comparator: 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.

Experimental: 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.

Experimental: 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.

Experimental: 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.

Experimental: 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.

Experimental: 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.


Other interventions: Guselkumab
Guselkumab will be administered as subcutaneous injection.

Other interventions: Golimumab
Golimumab will be administered as subcutaneous injection.

Other interventions: JNJ-78934804
JNJ-78934804 will be administered subcutaneously as per defined regimen.

Treatment: Drugs: Placebo
Placebo will be administered as subcutaneous injection.
Intervention code [1] 0 0
Other interventions
Intervention code [2] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Percentage of Participants with Clinical Remission at Week 48
Timepoint [1] 0 0
Week 48
Primary outcome [2] 0 0
Percentage of Participants with Endoscopic Response at Week 48
Timepoint [2] 0 0
Week 48
Secondary outcome [1] 0 0
Percentage of Participants with Patient-reported Outcomes (PRO)-2 Remission at Week 48
Timepoint [1] 0 0
Week 48
Secondary outcome [2] 0 0
Percentage of Participants with Endoscopic Remission at Week 48
Timepoint [2] 0 0
Week 48
Secondary outcome [3] 0 0
Percentage of Participants with Clinical Remission at Week 24
Timepoint [3] 0 0
Week 24
Secondary outcome [4] 0 0
Percentage of Participants with Endoscopic Response at Week 24
Timepoint [4] 0 0
Week 24
Secondary outcome [5] 0 0
Percentage of Participants with Adverse Events (AEs)
Timepoint [5] 0 0
Up to Week 48
Secondary outcome [6] 0 0
Percentage of Participants with Serious Adverse Events (SAEs)
Timepoint [6] 0 0
Up to Week 48
Secondary outcome [7] 0 0
Serum Concentrations of Guselkumab Over Time
Timepoint [7] 0 0
Up to Week 48
Secondary outcome [8] 0 0
Serum Concentrations of Golimumab Over Time
Timepoint [8] 0 0
Up to Week 48
Secondary outcome [9] 0 0
Percentage of Participants with Antibodies to Guselkumab
Timepoint [9] 0 0
Up to Week 48
Secondary outcome [10] 0 0
Titers of Antibodies to Guselkumab
Timepoint [10] 0 0
Up to Week 48
Secondary outcome [11] 0 0
Percentage of Participants with Antibodies to Golimumab
Timepoint [11] 0 0
Up to Week 48
Secondary outcome [12] 0 0
Titers of Antibodies to Golimumab
Timepoint [12] 0 0
Up to Week 48
Secondary outcome [13] 0 0
Percentage of Participants with Neutralizing Antibodies to Guselkumab.
Timepoint [13] 0 0
Up to Week 48
Secondary outcome [14] 0 0
Percentage of Participants with Neutralizing Antibodies to Golimumab
Timepoint [14] 0 0
Up to Week 48

Eligibility
Key inclusion criteria
- 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's disease activity
index (CDAI), stool frequency (SF), abdominal pain (AP) score and simple endoscopic
score for Crohn's disease (SES-CD)

- Demonstrated inadequate response, loss of response, or intolerance to at least one
biologic approved for the treatment of Crohn's disease

- If female and of childbearing potential, must meet the contraception and reproduction
requirements
Minimum age
18 Years
Maximum age
65 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- Complications of CD that may be anticipated to require surgery

- Currently has or is suspected to have an abscess. Recent cutaneous and perianal
abscesses are not exclusionary if drained and adequately treated at least 3 weeks
before baseline, or 8 weeks before baseline for intra-abdominal abscesses, provided
that there is no anticipated need for any further surgery

- Has had any kind of bowel resection within 24 weeks, or any other intra-abdominal or
other major surgery within 12 weeks

- Has a draining (example, functioning) stoma or ostomy

- Currently has a malignancy or has a history of malignancy within 5 years before
screening (with the exception of a nonmelanoma skin cancer or cervical carcinoma in
situ that has been adequately treated with no evidence of recurrence for greater than
or equal do (>=) 12 months before the first dose of study intervention)

- 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

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 2
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
22/07/2022
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
27/03/2029
Actual
Sample size
Target
715
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
The Queen Elizabeth Hospital - Adelaide
Recruitment hospital [2] 0 0
Box Hill Hospital - Box Hill
Recruitment hospital [3] 0 0
Monash Health, Monash Medical Centre - Clayton
Recruitment hospital [4] 0 0
Western Health - Footscray
Recruitment hospital [5] 0 0
St Vincent's hospital - Melbourne
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Royal Prince Alfred Hospital - Newtown
Recruitment hospital [7] 0 0
Royal Adelaide Hospital - North Terrace
Recruitment hospital [8] 0 0
Royal Melbourne Hospital - Parkville
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5011 - Adelaide
Recruitment postcode(s) [2] 0 0
3128 - Box Hill
Recruitment postcode(s) [3] 0 0
3168 - Clayton
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3011 - Footscray
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3002 - Melbourne
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2042 - Newtown
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5000 - North Terrace
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3050 - Parkville
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Wolverhampton.

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Janssen Research & Development, LLC
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
The purpose of this study is to evaluate the efficacy of JNJ-78934804 at Week 48 compared to
guselkumab and golimumab.
Trial website
https://clinicaltrials.gov/ct2/show/NCT05242471
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Janssen Research & Development, LLC Clinical Trial
Address 0 0
Janssen Research & Development, LLC
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Study Contact
Address 0 0
Country 0 0
Phone 0 0
844-434-4210
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT05242471