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A Phase I Dose Escalation Trial of PR104 Given Weekly in Subjects With Solid Tumors

Unspecified Adult Solid Tumor, Protocol Specific Clinical Trial

Official title:
A Phase I, Multi-center, Open-label, Dose Escalation Trial of the Safety and Pharmacokinetics of Intravenous PR104 Given Weekly in Subjects With Solid Tumors

Clinical Trial Summary

The purpose of this study is to determine the side effects and best weekly dose of PR104 in patients with advanced solid tumors.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

  • Unspecified Adult Solid Tumor, Protocol Specific
Clinical Trial Details
NCT number NCT01358227
Study type Interventional
Source Proacta, Incorporated
Contact
Status Completed
Phase Phase 1
Start date December 2006
Completion date January 2010
View Details
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