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Completed Phase 1 Interventional

Study of CC-122 to Evaluate the Safety, Tolerability, and Effectiveness for Patients With Advanced Solid Tumors, Non-Hodgkin's Lymphoma, or Multiple Myeloma

ClinicalTrials.gov ID: NCT01421524

Public ClinicalTrials.gov record NCT01421524. 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 Jul 22, 2026, 11:52 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 1a/1b, Multi-center, Open-label, Dose Finding Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of the Pleiotropic Pathway Modifier CC-122 Administered Orally to Subjects With Advanced Solid Tumors, Non-Hodgkin's Lymphoma, or Multiple Myeloma.

Study identification

NCT ID
NCT01421524
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Celgene
Industry
Enrollment
271 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
Sep 11, 2011
Primary completion
Nov 20, 2023
Completion
Nov 20, 2023
Last update posted
Dec 11, 2023

2011 – 2023

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
City of Hope Cancer Center Duarte California 91010-300
UCLA Neuro-Oncology Program Los Angeles California 90095
UCSF Helen Diller Medical Center at Parnassus Heights San Francisco California 94143-1270
University Of Michigan Comprehensive Cancer Center Ann Arbor Michigan 48109
Henry Ford Medical Center - New Center One Detroit Michigan 48202-268
Comprehensive Cancer Centers Of Nevada Las Vegas Nevada 89169
Rutgers Cancer Institute of New Jersey University New Brunswick New Jersey 08901
Mount Sinai Hospital New York New York 10029
Local Institution - 020 New York New York 10065
Levine Cancer Institute Charlotte North Carolina 28204
MUSC Rheumatology and Immunology Dept. Charleston South Carolina 29425
Greenville Hospital System Greenville South Carolina 29605
Sarah Cannon Research Institute Drug Development Unit Nashville Tennessee 37203
Texas Oncology, PA - Dallas 75246 Dallas Texas 75246
South Texas Accelerated Research Therapeutics (START) San Antonio Texas 78229
Swedish Medical Center Cancer Institute Research Seattle Washington 98104
Yakima Valley Memorial Hospital/ North Star Lodge Yakima Washington 98902

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 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01421524, 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 Dec 11, 2023 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01421524 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →