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

Status:	Completed
Conditions:	Cancer
Therapuetic Areas:	Oncology
Healthy:	No
Age Range:	18 - Any
Updated:	11/4/2018
Start Date:	January 22, 2015
End Date:	October 17, 2018

An Open-Label Study to Evaluate the Pharmacokinetics of Doxorubicin Following the Concomitant Intravenous Administration of Olaratumab (IMC-3G3) to Patients With Advanced Soft Tissue Sarcoma

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.

Inclusion Criteria:

- 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

Exclusion Criteria:

- 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

We found this trial at

sites

UCLA Medical Center

757 Westwood Plaza
Los Angeles, California 90024

(310) 825-9111