A Study of Guselkumab in Participants With Familial Adenomatous Polyposis
Launched by JANSSEN RESEARCH & DEVELOPMENT, LLC · Aug 27, 2018
Trial Information
Current as of August 02, 2025
Completed
Keywords
ClinConnect Summary
Familial adenomatous polyposis (FAP) is the most common polyposis syndrome. It is autosomal dominant inherited disorder characterized by early onset of hundreds to thousands of adenomatous polyps throughout colon. If left untreated, this syndrome may develop colorectal cancer (CRC). Polyps from individuals with FAP display inflammatory features associated with activation of interleukin (IL) 23/IL 17/JAK/STAT3 pathway. This inflammation is thought to contribute to further mutagenesis, culminating in tumor development. Specifically, IL-23 is linked to tumor growth and progression in CRC. Guse...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Phenotypic familial adenomatous polyposis (FAP) with disease involvement of the colorectum by either genetic or clinical diagnosis: Adenomatous polyposis coli (APC) germline mutation with or without family history, or with greater than (\>)100 adenomas in large intestine and a family history of FAP, attenuated FAP is allowed. FAP phenotype post colectomy for polyposis with a family history of FAP may be allowed
- • Post-colectomy or subtotal colectomy
- • Polyps with a sum of diameters greater than or equal to (\>=)10 millimeter (mm) in the rectum or pouch on biopsy at screening
- • A woman of childbearing potential must agree not to get pregnant during the study and at least 12 weeks after the last dose of study administration
- • A woman must agree not to breast feed or donate eggs (ova, oocytes) during the study and for a period of 12 weeks after the last administration of study drug
- Exclusion Criteria:
- • Prior use of any biologic therapy targeting interleukin (IL)-12/23, IL-17, or IL-23 receptor
- • Use of non-steroidal anti-inflammatory drugs other than aspirin during the study. The use 100 milligram (mg) of aspirin a day or 700 mg of aspirin per week is allowed
- • Treatment with other FAP-directed drug therapy (including NSAID \[Nonsteroidal anti-inflammatory drug\] drugs), unless completes a 4-week washout period prior to randomization
- • High grade dysplasia or cancer on biopsy at screening in GI tract (including stomach, duodenum, and colon/rectum/pouch)
- • Duodenal, colorectal, or pouch polyp: \>2 centimeter (cm) unless excised at the screening evaluation; and 1 to 2 cm with evidence of high-grade dysplasia upon biopsy unless excised
About Janssen Research & Development, Llc
Janssen Research & Development, LLC, a subsidiary of Johnson & Johnson, is a leading pharmaceutical company dedicated to advancing innovative therapies in multiple therapeutic areas, including oncology, immunology, neuroscience, infectious diseases, and cardiovascular health. With a strong commitment to scientific excellence and patient-centered research, Janssen leverages cutting-edge technology and collaborative partnerships to drive the development of transformative treatments. The company is focused on addressing unmet medical needs through rigorous clinical trials and a robust pipeline, aiming to improve health outcomes and enhance the quality of life for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
New Haven, Connecticut, United States
Tampa, Florida, United States
Boston, Massachusetts, United States
Seattle, Washington, United States
Saint Louis, Missouri, United States
Philadelphia, Pennsylvania, United States
Jacksonville, Florida, United States
Boston, Massachusetts, United States
Duarte, California, United States
Miami, Florida, United States
Cleveland, Ohio, United States
Houston, Texas, United States
Ulm, , Germany
Leiden, , Netherlands
New Haven, Connecticut, United States
Phoenix, Arizona, United States
Rotterdam, , Netherlands
Stockholm, , Sweden
New Orleans, Louisiana, United States
Ulm, , Germany
Tel Aviv, , Israel
Amsterdam, , Netherlands
Columbus, Ohio, United States
Salt Lake City, Utah, United States
Bonn, , Germany
Warszawa, , Poland
Barcelona, , Spain
Poznan, , Poland
Marseille, , France
New York, New York, United States
Philadelphia, Pennsylvania, United States
Lyon, , France
Río Piedras, , Puerto Rico
Madrid, , Spain
Rio Piedras, , Puerto Rico
Warszawa, , Poland
New York, New York, United States
Barcelona, , Spain
Barcelona, , Spain
Poznan, , Poland
Patients applied
Trial Officials
Janssen Research & Development, LLC Clinical Trial
Study Director
Janssen Research & Development, LLC
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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