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Completed Phase 2 Interventional Results available

Study to Evaluate the Efficacy and Safety of CUDC-907 in Patients With RR DLBCL, Including Patients With MYC Alterations

ClinicalTrials.gov ID: NCT02674750

Public ClinicalTrials.gov record NCT02674750. 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 7, 2026, 7:50 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

Open-Label, Phase 2 Study to Evaluate the Efficacy and Safety of CUDC-907 in Patients With Relapsed/Refractory Diffuse Large B-Cell Lymphoma, Including Patients With MYC Alterations

Brief summary

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

This is a Phase 2, open-label, multicenter trial designed to evaluate the efficacy and safety of CUDC-907 in subjects 18 years and older with Relapsed/Refractory (RR) MYC-altered Diffuse Large B-Cell Lymphoma (DLBCL).

Study identification

NCT ID
NCT02674750
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Curis, Inc.
Industry
Enrollment
70 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
Jun 30, 2016
Primary completion
May 27, 2019
Completion
May 27, 2019
Last update posted
Apr 26, 2022

2016 – 2019

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
University of California San Francisco-Fresno Fresno California 93701
University of Southern California, Norris Comprehensive Cancer Center Los Angeles California 90033
Moffitt Cancer Center Tampa Florida 33612
Winship Cancer Institute of Emory University Atlanta Georgia 30322
University of Chicago Chicago Illinois 60647
Norton Cancer Institute Louisville Kentucky 40207
Karmanos Cancer Institute Detroit Michigan 48201
Mayo Clinic Rochester Minnesota 55905
University of Rochester Rochester New York 55905
University of Oklahoma Health Sciences Center (OUHSC) Oklahoma City Oklahoma 73104
Cancer Care Associates Tulsa Oklahoma 74104
Penn State Hershey Cancer Institute-Clinical Trials Office Hershey Pennsylvania 17033
Hospital of the University of Pennsylvania Philadelphia Pennsylvania 19104
Fox Chase Cancer Center Philadelphia Pennsylvania 19111
University of Tennessee Cancer Center Knoxville Tennessee 37920
Tennessee Oncology Sarah Cannon Nashville Tennessee 37203
Charles A. Sammons Cancer Center Dallas Texas 75246
Houston Methodist Hospital Houston Texas 77030
The University of Texas M.D. Anderson Cancer Center Houston Texas 77030
Swedish Cancer Institute Seattle Washington 98104

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02674750, 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 Apr 26, 2022 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02674750 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →