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Study of Two Dose Levels of RTA 402 in Patients With Advanced Malignant Melanoma

2014-08-27 03:35:59 | BioPortfolio

Summary

The primary purpose of the study is to determine the proportion of patients without progression at 6-months in patients with unresectable Stage III or Stage IV melanoma who are taking RTA 402.

Description

This is a phase II, open label, randomized study in patients with unresectable Stage III or Stage IV malignant melanoma. Patients will be randomly assigned to two different doses of RTA 402 administered orally once daily for 28 consecutive days, for up to 18 months.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Masking: Open Label, Primary Purpose: Treatment

Conditions

Malignant Melanoma

Intervention

RTA 402

Status

Withdrawn

Source

Reata Pharmaceuticals, Inc.

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:35:59-0400

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Medical and Biotech [MESH] Definitions

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