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Completed Phase 1 Interventional

Phase 1 Study to Evaluate MEDI4736 in Subjects With Myelodysplastic Syndrome

ClinicalTrials.gov ID: NCT02117219

Public ClinicalTrials.gov record NCT02117219. 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 2, 2026, 3:23 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 1 Study to Evaluate the Safety and Tolerability of MEDI4736 as Monotherapy or in Combination With Tremelimumab With or Without Azacitidine in Subjects With Myelodysplastic Syndrome After Treatment With Hypomethylating Agents

Brief summary

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

This is a multicenter, open-label, Phase 1 study to assess the safety and antitumor activity of MEDI4736 as Monotherapy or in Combination with Tremelimumab with or without Azacitidine in Subjects with myelodysplastic syndrome after treatment with hypomethylating agents

Study identification

NCT ID
NCT02117219
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
MedImmune LLC
Industry
Enrollment
67 participants

Conditions and interventions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
18 Years to 99 Years
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
May 19, 2014
Primary completion
Apr 29, 2019
Completion
Apr 29, 2019
Last update posted
May 9, 2019

2014 – 2019

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
Research Site Scottsdale Arizona 85259
Research Site Los Angeles California 90095
Research Site New Haven Connecticut 06520-8063
Research Site Tampa Florida 33612
Research Site Atlanta Georgia 30322
Research Site Chicago Illinois 60637
Research Site Baltimore Maryland 21201
Research Site Boston Massachusetts 02215
Research Site Detroit Michigan 48201
Research Site Rochester Minnesota 55905
Research Site New York New York 10029
Research Site New York New York 10065
Research Site Greenville South Carolina 29601
Research Site Houston Texas 77030
Research Site San Antonio Texas 78229
Research 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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02117219, 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 May 9, 2019 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02117219 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →