A Study of Olaratumab (LY3012207) Plus Pembrolizumab in Participants With Advanced or Metastatic Soft Tissue Sarcoma

Completed · Phase 1

Conditions studied: Soft Tissue Sarcoma

In brief

The purpose of this study is to evaluate the safety of olaratumab plus pembrolizumab in participants with previously treated advanced or metastatic soft tissue sarcoma.

Key facts

Study ID

NCT03126591

Run by

Eli Lilly and Company

People needed

41

Starts

2017-07-03

Expected to finish

2023-02-21

Last updated by the study team

2024-10-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologically confirmed diagnosis of advanced unresectable or metastatic STS, not amenable to curative treatment and after available standard therapies have failed to provide clinical benefit. Note: Participants with a diagnosis of Grade 1 liposarcoma (atypical lipomatous neoplasms) are eligible if there is histological or radiographic evidence of evolution to more aggressive disease.
• Presence of measurable or nonmeasurable but evaluable disease as defined by the Response Evaluation Criteria in Solid Tumors (RECIST 1.1).
• Performance status 0-1 on the Eastern Cooperative Oncology Group (ECOG) scale.
• Must be able to provide tumor tissue obtained within 6 months of study enrollment. If such tissue is not available, a newly obtained core or excisional biopsy of a tumor lesion must be performed.
• Have an anticipated life expectancy of ≥3 months.

You may not qualify if…

• Have received any previous systemic therapy (including investigational agents) targeting PD-1/programmed cell death ligand 1 (PDL-1) or PD-1/PDL-2 signaling pathways (including previous participation in Merck MK-3475 trials). Prior treatment with olaratumab is allowed. Prior therapy with other immune checkpoint inhibitors, including but not limited to, anti-CD137 antibody or anti-cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) antibody, is not permitted.
• Have known active central nervous system (CNS) metastasis and/or carcinomatous meningitis. Participants with treated CNS metastases are eligible for this study if they have not received corticosteroids and/or anticonvulsants within 7 days of study treatment, and their disease is asymptomatic and radiographically stable for at least 60 days.
• Have active autoimmune disease or other syndrome that requires systemic steroids or autoimmune agents in the past 2 years.
• History of interstitial lung disease or non-infectious pneumonia.
• Have received a live-virus vaccine within 30 days prior to planned treatment start.
• Have histologically or cytologically confirmed Kaposi's sarcoma or gastrointestinal stromal tumor (GIST).
• Have inflammatory bowel disease for which the participant has used immunosuppressive agents within the last 2 years.

Where it is running

• Dana Farber Cancer Institute — Boston, Massachusetts, United States
• Memorial Sloan Kettering Cancer Center — New York, New York, United States
• University of Pittsburgh Medical Center — Pittsburgh, Pennsylvania, United States
• Universitaire Ziekenhuizen Leuven - Campus Gasthuisberg — Leuven, Belgium
• Herlev and Gentofte Hospital — Herlev, Denmark
• Gustave Roussy — Villejuif, France

Full record on ClinicalTrials.gov

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