A Study of Olaratumab in Soft Tissue Sarcoma
Public ClinicalTrials.gov record NCT01185964. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Phase 1b/2, With Phase 2 Randomized, Study Evaluating the Efficacy of Doxorubicin With or Without a Human Anti-PDGFRα Monoclonal Antibody (IMC-3G3) in the Treatment of Advanced Soft Tissue Sarcoma
Study identification
- NCT ID
- NCT01185964
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 1, Phase 2
- Lead sponsor
- Eli Lilly and Company
- Industry
- Enrollment
- 148 participants
Conditions and interventions
Conditions
Interventions
- Olaratumab Biological
- doxorubicin Drug
Biological · Drug
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Sep 30, 2010
- Primary completion
- Jul 31, 2014
- Completion
- Mar 31, 2016
- Last update posted
- Apr 13, 2017
2010 – 2016
United States locations
- U.S. sites
- 17
- U.S. states
- 16
- U.S. cities
- 17
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| ImClone Investigational Site | Tucson | Arizona | 85724 | — |
| ImClone Investigational Site | Los Angeles | California | 90024 | — |
| ImClone Investigational Site | Aurora | Colorado | 80045 | — |
| ImClone Investigational Site | Gainesville | Florida | 32608 | — |
| ImClone Investigational Site | Orlando | Florida | 32806 | — |
| ImClone Investigational Site | Atlanta | Georgia | 30308 | — |
| ImClone Investigational Site | Chicago | Illinois | 60611 | — |
| ImClone Investigational Site | Rochester | Minnesota | 55902 | — |
| ImClone Investigational Site | St Louis | Missouri | 63110 | — |
| ImClone Investigational Site | New York | New York | 10065 | — |
| ImClone Investigational Site | Charlotte | North Carolina | 28203 | — |
| ImClone Investigational Site | Cleveland | Ohio | 44106 | — |
| ImClone Investigational Site | Charleston | South Carolina | 29425 | — |
| ImClone Investigational Site | Memphis | Tennessee | 38119 | — |
| ImClone Investigational Site | San Antonio | Texas | 78229 | — |
| ImClone Investigational Site | Seattle | Washington | 98109 | — |
| ImClone Investigational Site | Madison | Wisconsin | 53792 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT01185964, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Apr 13, 2017 · Synced Jul 23, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01185964 live on ClinicalTrials.gov.