CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 49 enrolled
Drug / intervention
Olaratumab +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02326025
NCT02326025Phase 1Completed

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

Eli Lilly and Company·interventional·Posted Dec 25, 2014·Updated Nov 21, 2019

In Brief

A Phase 1 clinical trial evaluating Olaratumab and Doxorubicin for Sarcoma, Soft Tissue. Completed, enrolled 49 participants across 6 sites.

Detailed Summary

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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 1CompletedFinished
201520162017201820192020202120222023202420252026
First PostedDec 25, 2014
Enrollment StartJan 22, 2015
Primary CompletionMay 20, 2015
Study CompletionNov 2, 2018
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 11.5 years ago

Interventions

Olaratumabdrug

Administered IV

Doxorubicindrug

Administered IV