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CRLX101 alone or with bevacizumab or mFOLFOX6 in advanced solid tumors

NCT02648711Phase 1Terminated

Sponsor
Lumos Pharma, Inc.
Start
Oct 2015
Primary completion
Oct 2017
Modality
Polymer-based Nanoparticles
Countries
1
01

Overview

Phase 1, open-label trial of CRLX101 in solid tumor (3 arms), sponsored by Lumos Pharma, Inc. Primary endpoint: Maximum Tolerated Dose and/or Recommended Phase 2 Dose at 15 months. Started Oct 2015; status: terminated.

02

Drugs

CRLX101
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Conditions

solid tumor

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