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  • A Study of JNJ-64251330 in Participants With Familial Adenomatous Polyposis

A Study of JNJ-64251330 in Participants With Familial Adenomatous Polyposis

Principal Investigator

Daniel Sussman

Enrollment Status

Closed

Clinical Trial ID

Institutional Protocol # 20210943
National Clinical Trials Identifier NCT05014360

Clinical Trial Summary

The purpose of this study is to determine the effect of JNJ-64251330 in participants with
Familial Adenomatous Polyposis (FAP) on colorectal polyp burden (sum of the polyp diameters).


Phase

Phase 1


Funding Agency/Sponsor

Industrial


Disease

Colorectal Cancer


Enrollment Eligibility

Inclusion Criteria:
- Genetic diagnosis of classical familial adenomatous polyposis (FAP) (adenomatous
polyposis coli [APC] germline mutation or obligate carrier) with disease involvement
of the colorectum
- At least 6 polyps greater than or equal to (>=) 2 millimeters (mm) in diameter in the
rectum or colon
- A female participant of childbearing potential must have a negative highly sensitive
pregnancy test at screening and within 72 hours prior to the first dose of study drug
and must agree to further pregnancy tests during the study
- A male participant must agree not to donate sperm for the purpose of reproduction
during the study and for a minimum of 90 days after receiving the last dose of study
drug
- Must sign an informed consent form (ICF) indicating he or she understands the purpose
of the study and procedures required for the study and is willing to participate in
the study. Consent is to be obtained prior to the initiation of any study-related
tests or procedures that are not part of standard of care for the participant's
disease
Exclusion Criteria:
- Use of non-steroidal anti-inflammatory drugs (example, aspirin, ibuprofen) exceeding 5
days per month or exceeding the nonprescription dose, unless the participant completes
a 4-week washout period prior to the first dose of study drug
- Treatment with other FAP-directed drug therapy (including sulindac or celecoxib),
unless completes a 4-week washout period prior to the first dose of study drug
- History of human immunodeficiency virus (HIV)
- History of severe, progressive, or uncontrolled renal, genitourinary, hepatic,
hematologic, endocrine, cardiac, vascular, pulmonary, rheumatologic, neurologic,
psychiatric, or metabolic disturbances, or signs and symptoms thereof
- A history of, or ongoing, chronic or recurrent infectious disease including latent or
active tuberculosis (TB)


Contact Information

Phone Number +1 (305) 2436405
Get detailed information on ClinicalTrials.Gov

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