Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Approved For Marketing No phase listed Expanded access

Pomalidomide (POM) in Combination With Low Dose Dexamethasone (LD-Dex) in Patients With Relapsed or Refractory Multiple Myeloma

ClinicalTrials.gov ID: NCT01632826

Public ClinicalTrials.gov record NCT01632826. 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 Oct 22, 2026, 10:45 PM 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 Multicenter, Single-Arm, Open-Label Treatment Use Protocol for Pomalidomide (POM) in Combination With Low Dose Dexamethasone (LD-Dex) in Patients With Relapsed or Refractory Multiple Myeloma

Brief summary

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

To provide pomalidomide access to relapsed/refractory multiple myeloma subjects with a likelihood of benefit from the pomalidomide treatment while the medication is not commercially available

Study identification

NCT ID
NCT01632826
Recruitment status
Approved For Marketing
Study type
Expanded access
Phase
Not listed
Lead sponsor
Celgene
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Not listed

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

Study timeline

Start date
Not listed
Primary completion
Not listed
Completion
Not listed
Last update posted
Nov 12, 2019

United States locations

U.S. sites
25
U.S. states
20
U.S. cities
24
Facility City State ZIP Site status
Celgene Study Site Duarte California 91010 —
Celgene Study Site Greenbrae California 94904 —
Celgene Study Site Los Angeles California 90048 —
Celgene Study Site Denver Colorado 80218 —
Celgene Study Site West Palm Beach Florida 33401 —
Celgene Study Site Marietta Georgia 30060 —
Celgene Study Site Peoria Illinois 61615 —
Celgene Study Site Indianapolis Indiana 46202 —
Celgene Study Site Iowa City Iowa 52242 —
Celgene Study Site Baltimore Maryland 21215 —
Celgene Study Site Hyannis Massachusetts 02601 —
Celgene Study Site St Louis Missouri 63110 —
Celgene Study Site Omaha Nebraska 68198 —
Celgene Study Site Hackensack New Jersey 07601 —
Celgene Study Site New York New York 10016 —
Celgene Study Site New York New York 10029 —
Celgene Study Site Philadelphia Pennsylvania 19107 —
Celgene Study Site Sellersville Pennsylvania 18960 —
Celgene Study Site Greenville South Carolina 29615 —
Celgene Study Site Sioux Falls South Dakota 57105 —
Celgene Study Site Dallas Texas 75390 —
Celgene Study Site Houston Texas 77030 —
Celgene Study Site Salt Lake City Utah 84106 —
Celgene Study Site Morgantown West Virginia 26506 —
Celgene Study Site Milwaukee Wisconsin 53226 —

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01632826, 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 Nov 12, 2019 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01632826 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →