Familial Adenomatous Polyposis

Disease

Disease Profile

Familial adenomatous polyposis (FAP) is an inherited colorectal cancer predisposition syndrome characterized by development of numerous adenomatous polyps in the large intestine. It is caused most commonly by pathogenic APC variants and, if untreated, carries a very high risk of colorectal cancer. Disease typically begins in adolescence or early adulthood.

Category
Inherited colorectal cancer predisposition syndrome
Prevalence
Estimated frequency is about 1 in 10,000 to 1 in 15,000

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Related Clinical Trials

NCT ID Title Status Phase
NCT07199127

Duodenal Polyposis Classification in FAP

RECRUITING
NCT06641310

Trial of Exercise Therapy in Familial Adenomatous Polyp (FAP)

RECRUITING NA
NCT06614738

Microbial and Environmental Factors Associated with Polyps Development in Familial Adenomatous Polyposis (MicrobEnvironment in FAP)

RECRUITING
NCT06578637

Investigation of β-hydroxybutyrate Supplementation as Chemoprevention in Familial Adenomatous Polyposis

RECRUITING NA
NCT06557733

An Investigational Drug (TPST-1495) in Patients With Familial Adenomatous Polyposis

RECRUITING PHASE2
NCT06545526

Chemopreventive Effect of Combination of Celecoxib and Metformin in Patients With Familial Adenomatous Polyposis

RECRUITING PHASE3
NCT06538402

Ten Versus Fifteen Centimeter Pouch in IPAA Surgery

RECRUITING NA
NCT06435533

Cold Atmospheric Plasma for the Endoscopic Treatment of Duodenal Polyps in Patients With Familial Adenomatous Polyposis

RECRUITING NA
NCT06308445

Safety Study for the Use of Rapamycin in Children With Familial Adenomatous Polyposis

NOT_YET_RECRUITING PHASE2
NCT06163365

Inherited Cancer Early Diagnosis (ICED) Study

RECRUITING