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Recruiting Phase 3 Interventional

Phase 3 Trial of eRapa in Patients With Familial Adenomatous Polyposis

ClinicalTrials.gov ID: NCT06950385

Public ClinicalTrials.gov record NCT06950385. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 7:53 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Multi-Site, Prospective, Randomized, Double-Blind, Placebo-Controlled Trial of eRapa to Improve Clinical Outcomes in Patients With Familial Adenomatous Polyposis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The main goal of this clinical trial is to learn if the drug eRapa works to slow down the progression of disease in patients diagnosed with Familial Adenomatous Polyposis (FAP). Researchers will compare eRapa to Placebo. The questions to be answered by this trial are: * Does taking eRapa help to slow down the progression of the disease in patients with FAP? * Is eRapa a safe treatment for patients diagnosed with FAP? * What is the effect of eRapa on the number of polyps found in GI tract of patients diagnosed with FAP? * How does treatment with eRapa affect a patient's quality of life? Participants will: * Take eRapa or placebo once per day every other week until disease progresses (gets worse), stops taking part in the trial or dies. * Visit the clinic once every 3 months for check ups and tests. * Have an endoscopy at the start of the trial and then every 6 months to check on whether the disease is getting better or worse.

Study identification

NCT ID
NCT06950385
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Rapamycin Holdings Inc.
Industry
Enrollment
168 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 17, 2025
Primary completion
Jun 30, 2030
Completion
Dec 31, 2030
Last update posted
Jun 1, 2026

2025 – 2031

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
City of Hope Arcadia California 91007 Recruiting
Yale Cancer Center New Haven Connecticut 06520 Recruiting
Georgetown University Washington D.C. District of Columbia 20057 Recruiting
Digestive & Liver Center of Florida Orlando Florida 32825 Recruiting
Cleveland Clinic Florida Weston Florida 33331 Recruiting
University of Chicago Chicago Illinois 60615 Recruiting
University of Kansas Medical Center Kansas City Kansas 66160 Recruiting
Johns Hopkins University Baltimore Maryland 21205 Recruiting
Dana Farber Cancer Institute Boston Massachusetts 02115 Recruiting
University of Michigan Ann Arbor Michigan 48109 Recruiting
Department of Surgery, Section of Colon Rectal and Surgery St Louis Missouri 63110 Recruiting
Cleveland Clinic Cleveland Ohio 44195 Recruiting
Ohio State University Columbus Ohio 43210 Recruiting
Geisinger Medical Center Danville Pennsylvania 17822 Recruiting
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213 Recruiting
The University of Texas MD Anderson Cancer Center Houston Texas 77030 Recruiting
Benaroya Research Institute at Virginia Mason Seattle Washington 98101 Recruiting
University of Washington - Fred Hutchinson Seattle Washington 98195 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06950385, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 1, 2026 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06950385 live on ClinicalTrials.gov.

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