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Completed Phase 1 Interventional Results available

MSB0011359C (M7824) in Metastatic or Locally Advanced Solid Tumors

ClinicalTrials.gov ID: NCT02517398

Public ClinicalTrials.gov record NCT02517398. 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 10, 2026, 12:47 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 Phase I, Open-label, Multiple-ascending Dose Trial to Investigate the Safety, Tolerability, PK, Biological and Clinical Activity of MSB0011359C in Subjects With Metastatic or Locally Advanced Solid Tumors and Expansion to Selected Indications

Brief summary

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

The main purpose of this Phase I study was to test MSB0011359C (M7824) at different dose levels to see if it is safe and well tolerated when given once every 2 weeks. Phase I means the study drug has not previously been given to humans or has only been given to a limited number of people, although it has been extensively studied in animals. Based on this information, it is hoped to find out which dose could be best for the treatment of patients. There are two parts of this research study: a dose-escalation part and an expansion part. Dose escalation means that the first people taking part in the study will receive low doses of the study drug, and as more people take part, the additional participants will receive a higher dose. This is done to find the safest dose for the study drug. Expansion means that after the dose-escalation part of the study has looked at the safety and effectiveness of different doses, many more people will be invited to take part in the study and will receive the study drug at the safest dose. Additional purposes of the study are to find out whether the study drug has anti-cancer effects and how the study drug is processed by the body.

Study identification

NCT ID
NCT02517398
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
600 participants

Conditions and interventions

Conditions

Interventions

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
Aug 30, 2015
Primary completion
May 22, 2022
Completion
May 22, 2022
Last update posted
May 2, 2024

2015 – 2022

United States locations

U.S. sites
36
U.S. states
21
U.S. cities
35
Facility City State ZIP Site status
Arizona Clinical Research Center Tucson Arizona 85715
Pacific Oncology Associates Escondido California 92025
University of California Davis Health System Sacramento California 95817
California Pacific Medical Center San Francisco California 94118
Innovative Clinical Research Institute Whittier California 90603
Rocky Mountain Cancer Centers, LLP Denver Colorado 80218
Eastern Connecticut Hematology/Oncology Assoc. Norwich Connecticut 06360
Sylvester Cancer Center Miami Florida 33136
Hematology - Oncology Associates of Treasure Coast Port Saint Lucie Florida 34952
University Cancer & Blood Center, LLC Athens Georgia 30607
Southeastern Regional Medical Center Newnan Georgia 30265
Metairie Oncologists, LLC Metairie Louisiana 70006
National Cancer Institute Bethesda Maryland 20892
Dana Farber Cancer Institute Boston Massachusetts 02215
Henry Ford Health System Detroit Michigan 48202
Michigan State University Lansing Michigan 48910
Washington University St Louis Missouri 63110
Comprehensive Cancer Centers of Nevada Las Vegas Nevada 89169
University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599
UC Health Clinical Trials Office Cincinnati Ohio 45206
Case Comprehensive Cancer Center Cleveland Ohio 44106
Penn State University Milton S. Hershey Medical Center Hershey Pennsylvania 17033
Rhode Island Hospital Providence Rhode Island 02903
Medical University of South Carolina Charleston South Carolina 29425
Greenville Hospital System University Medical Center (ITOR) Greenville South Carolina 29605
Tennessee Cancer Specialists Knoxville Tennessee 37909
Texas Oncology, P.A. - Austin Austin Texas 78705
Mary Crowley Cancer Research Centers Dallas Texas 75230
Texas Oncology, P.A. - Fort Worth Fort Worth Texas 76104
Oncology Consultants, P.A. Houston Texas 77030
University of Texas M. D. Anderson Cancer Center - Investigational Cancer Therapeutics Houston Texas 77030
South Texas Accelerated Research Therapeutics, LLC San Antonio Texas 78229
Texas Oncology, P.A. - Tyler Tyler Texas 75702
Virginia Cancer Specialists, PC Fairfax Virginia 22031
Virginia Oncology Associates - Hampton Norfolk Virginia 23502
Compass Oncology Vancouver Washington 98684

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 82 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02517398, 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 2, 2024 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02517398 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →