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Completed Phase 1 Interventional

A Study of Atezolizumab Administered Alone or in Combination With Azacitidine in Participants With Myelodysplastic Syndromes

ClinicalTrials.gov ID: NCT02508870

Public ClinicalTrials.gov record NCT02508870. 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 24, 2026, 5:49 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 Ib Study of the Safety and Pharmacology of Atezolizumab (Anti-PD-L1 Antibody) Administered Alone or in Combination With Azacitidine in Patients With Myelodysplastic Syndromes

Study identification

NCT ID
NCT02508870
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
46 participants

Conditions and interventions

Interventions

  • Atezolizumab Drug
  • Azacitidine Drug

Drug

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 29, 2015
Primary completion
Jun 9, 2019
Completion
Jun 9, 2019
Last update posted
Aug 18, 2019

2015 – 2019

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
City of Hope Duarte California 91010
Stanford University Palo Alto California 94305
University of California, San Francisco, Helen Diller Family Comprehensive Cancer Center San Francisco California 94158
University of Colorado Hospital - Anschutz Cancer Pavilion Aurora Colorado 80045
University of Kansas Medical Center Westwood Kansas 66205
Dana Farber Cancer Institute Boston Massachusetts 02215
University of Nebraska Medical Center; UNMC Oncology/Hematology Omaha Nebraska 68198-7680
Roswell Park Cancer Institute; Grace Cancer Drug Center Buffalo New York 14263
Montefiore Einstein Cancer Center The Bronx New York 10461
Cleveland Clinic Foundation Cleveland Ohio 44915
Medical University of South Carolina; Hollings Cancer Center Charleston South Carolina 29425
Sarah Cannon Research Institute Nashville Tennessee 37203
The University of Texas MD Anderson Cancer Center Houston Texas 77030-4009
University of Virginia Health System; Hematology/Oncology Division Charlottesville Virginia 22908
Fred Hutchinson Cancer Research Center Seattle Washington 98109

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02508870, 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 Aug 18, 2019 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02508870 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →