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NCT03767257CompletedPhase 2

A Study of Colesevelam for Lenalidomide-Associated Diarrhea

A Phase 2 Study of Colesevelam for Lenalidomide-Associated Diarrhea

Source: ClinicalTrials.gov · Last updated 21 Oct 2025

Brief summary (registry, in English)

The purpose of this study is to test the safety of colesevelam and find out what effects, if any, colesevelam has on lenalidomide associated diarrhea in participants with multiple myeloma on lenalidomide maintenance.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
25 (actual)
First submitted
5 Dec 2018
Start date
3 Dec 2018
Primary completion date
27 Nov 2024
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT03767257

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 25
  • From 3 Dec 2018 to the primary completion date, 27 Nov 2024
  • 7 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients currently already receiving a bile acid sequestrant or have previously used bile acid sequestrant drugs for diarrhea and had no benefit
  • Patients with diarrhea secondary to infection. Stool studies for GI pathogens should be collected prior to starting colesevelam but do not need to be resulted prior to starting Day 1 dose of colesevelam, unless infection is suspected by the treating investigator, in which case (Clostridium difficile PCR when clinically indicated, GI pathogen panel, stool ova and parasites, Giardia and Cryptosporum stool antigen tests will need to be resulted at investigator discretion.)

Other illness

  • Patients with history of bowel obstruction
  • Patients wit history of hypertriglyceridemia-induced panreatitis
  • Patients with known hypersensitivity to colesevelam or any component to the formulation

Lab values

  • Patients with serum triglyceride levels \>300 mg/dL

Who the study is looking for

  • Memorial Sloan Kettering Cancer Center (MSK) confirmed diagnosis of multiple myeloma
  • Treatment with single agent lenalidomide maintenance
  • Patient must be \>/= 18 years of age at the time of informed consent
  • Experiencing grade 1 or more diarrhea according to the CTCAE 5.0 criteria for at least 4 out of 7 days preceding screening and study inclusion
  • Scheduled to receive lenalidomide maintenance cyles at MSK
  • Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests and other study procedures

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (7)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Memorial Sloan Kettering Basking Ridge (All Protocol Activities)
Coordinator of this site? Confirm its status
Basking RidgeUnited StatesUnknown status
Memorial Sloan Kettering Cancer Center Suffolk - Commack (All Protocol Activities)
Coordinator of this site? Confirm its status
CommackUnited StatesUnknown status
Memorial Sloan Kettering Westchester (All Protocol Activities)
Coordinator of this site? Confirm its status
HarrisonUnited StatesUnknown status
Memorial Sloan Kettering Monmouth (All Protocol Activities)
Coordinator of this site? Confirm its status
MiddletownUnited StatesUnknown status
Memorial Sloan Kettering Bergen
Coordinator of this site? Confirm its status
MontvaleUnited StatesUnknown status
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Memorial Sloan Kettering Nassau
Coordinator of this site? Confirm its status
UniondaleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.