CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 49 enrolled
Drug / intervention
MEDI-575drug
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/NCT00816400
NCT00816400Phase 1Completed

A Phase 1, Multicenter, Open-label, Single-arm, Dose-escalation Study to Evaluate the Safety, Tolerability, and Antitumor Activity of MEDI-575, a Fully Human Monoclonal Antibody Directed Against Platelet-derived Growth Factor Receptor Alpha (PDGFRα), in Subjects With Advanced Solid Tumors Refractory to Standard Therapy or for Which No Standard Therapy Exists

MedImmune LLC·interventional·Posted Jan 1, 2009·Updated Jun 26, 2018

In Brief

A Phase 1 clinical trial evaluating MEDI-575 for Cancer. Completed, enrolled 49 participants across 5 sites.

Detailed Summary

Evaluate the safety, tolerability and the tolerated maximum dose of MEDI-575 in adult subjects with advanced solid tumors refractory to standard therapy or for which no standard therapy exists.

Study Details

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

Timeline

Phase 1CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedJan 1, 2009
Enrollment StartMar 2, 2009
Primary CompletionJan 19, 2012
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 17.5 years ago

Interventions

MEDI-575drug

MEDI-575 as an IV infusion