A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial of Doxorubicin plus Olaratumab versus Doxorubicin plus Placebo in Patients with Advanced or Metastatic Soft Tissue Sarcoma

Eli Lilly and Company0 个研究点目标入组 460 人开始时间: 2015年10月5日最近更新: 2021年7月12日

适应症

试验速览

暂无简介。

•18 years or older at study entry
•Histologically confirmed diagnosis of locally advanced unresectable or metastatic STS not amenable to curative treatment with surgery or radiotherapy. Grade 1 liposarcoma are eligible if there is histological or radiographic evidence of evolution to more aggressive disease. (excludes GIST & Kaposi). Note: Evidence of disease progression is required for patients that are not newly diagnosed.
•Measurable or nonmeasurable but evaluable disease by RECIST 1.1
•May have had any number of prior systemic therapies for advanced/metastatic disease, however may not have received any previous treatment with anthracyclines. All previous anticancer treatments must be completed = 3 weeks (21 days) prior to first dose of study drug.
•Consent to provide archived FFPE tumor tissue or be subject to a pre-treatment re-biopsy of primary or metastatic tumor tissue future central pathology review and translational research (if archived tissue is unavailable)
•LVEF ›= 50%
•Life expectancy, in opinion of the investigator, is at least 3 months
•Females of child-bearing potential must have a negative serum pregnancy test within 7 days prior to randomization.
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•F.1.2 Adults (18-64 years) yes
•F.1.2.1 Number of subjects for this age range 350
•F.1.3 Elderly (>=65 years) yes
•F.1.3.1 Number of subjects for this age range 110

•Diagnosed with GIST or Kaposi sarcoma
•Active CNS or brain metastasis at randomization
•The patient has received prior treatment with doxorubicin, epirubicin, idarubicin, and/or other anthracyclines or anthracenediones; the patient has received treatment with olaratumab or has participated in a prior olaratumab trial.
•Prior radiotherapy of the mediastinal/pericardial area or whole pelvis radiation
•Electively planned or required major surgery during the study
•Uncontrolled intercurrent illness including, but not limited to, an ongoing/active infection requiring parenteral antibiotics, symptomatic congestive heart failure (CHF), left ventricular dysfunction (LVEF<50%), severe myocardial insufficiency, cardiac arrhythmia, cardiomyopathy, or a psychiatric illness/social situation that would limit compliance with study requirements
•Unstable angina pectoris, angioplasty, cardiac stenting, or myocardial infarction
•QTc interval › 450 msec and › 470 msec for males and females, respectively, on screening ECG
•Pregnant or breastfeeding
•Known active fungal, bacterial, or viral infection including human immunodeficiency virus (HIV) or viral (A, B, or C) hepatitis (screening is not required)

发起方