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Search / Trial NCT03649971

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.

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

0 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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