A Study of Olaratumab and Doxorubicin in Participants With Advanced Soft Tissue Sarcoma

Completed · Phase 1

Conditions studied: Sarcoma, Soft Tissue

In brief

The purpose of this study is to assess how the body handles olaratumab when it is given with another drug called doxorubicin. The safety and tolerability of these drugs will be studied. Each participant will complete two 21-day cycles in a fixed order. Participants who complete Cycle 2 may continue to receive olaratumab + doxorubicin for an additional six 21-day cycles and then may receive olaratumab alone until discontinuation criteria are met. Screening is required within 21 days prior to first dose. Part B was added in October, 2015 to assess how the body handles a higher dose of olaratumab when given with doxorubicin. Participants may only enroll in one part.

Key facts

Study ID

NCT02326025

Run by

Eli Lilly and Company

People needed

49

Starts

2015-01-22

Expected to finish

2018-11-02

Last updated by the study team

2019-11-21

Who can join

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

You may qualify if…

• Have histological or cytological evidence of a diagnosis of soft tissue sarcoma (STS) that is advanced and/or metastatic
• Have the presence of measurable and/or nonmeasurable disease
• Have given written informed consent prior to any study-specific procedures
• Have a performance status of less than or equal to 2 on the Eastern Cooperative Oncology Group (ECOG) scale
• Have discontinued previous treatments for cancer and recovered from the acute effects of therapy
• Are reliable and willing to make themselves available for the duration of the study and are willing to follow study procedures

You may not qualify if…

• Have received treatment within 28 days of the initial dose of study drug with an investigational product or non-approved use of a drug or device for noncancer indications
• Have received prior treatment with doxorubicin, daunorubicin, idarubicin, and/or other anthracyclines and anthracenediones
• Have active central nervous system (CNS) metastasis. Participants with treated CNS metastases are eligible for this study if they are not currently receiving corticosteroids
• Have unstable hepatic disease with a grade equal to or greater than Child-Pugh B
• Have an active fungal, bacterial, and/or known viral infection including human immunodeficiency virus (HIV) or viral (A, B, or C) hepatitis
• Have a history of another primary cancer, with the exception of a) curatively resected nonmelanoma skin cancer; b) curatively treated cervical carcinoma in situ; or c) other primary solid tumor treated with curative intent, no known active disease present, and no treatment administered during the last 3 years prior to study entry
• Have a history of chronic heart failure or left ventricular dysfunction
• Have a resting heart rate of less than (<)50 beats per minute (bpm) or greater than (>)100 bpm
• Have a history of radiation therapy involving the mediastinal/pericardial area. Previous radiation therapy is allowed but must not have included whole pelvis radiation

Where it is running

• UCLA Medical Center — Los Angeles, California, United States
• University of Colorado Cancer Center — Aurora, Colorado, United States
• Northwestern University — Chicago, Illinois, United States
• IU Simon Cancer Center — Indianapolis, Indiana, United States
• Washington University Medical Center — St Louis, Missouri, United States
• Seattle Cancer Care Alliance — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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