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Sym004 in Patients With Advanced Solid Tumors

2014-07-23 21:09:19 | BioPortfolio

Summary

This trial is designed as a multi-centre, open label, dose-escalation, phase I trial and consists of two parts. Part A investigates the safety and PK of escalating doses of Sym004 in patients with recurrent advanced solid tumors. Part B validates the safety and PK of Sym004 at the MTD in a homogenous patient population with advanced mCRC and wild-type KRAS. Part B will be initiated when a safe dose has been established in Part A.

Study Design

Allocation: Non-Randomized, Control: Uncontrolled, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

Advanced Solid Tumors

Intervention

Sym004

Location

South Texas Accelerated Research Therapeutics (START)
San Antonio
Texas
United States
78229

Status

Recruiting

Source

Symphogen A/S

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-07-23T21:09:19-0400

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