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August 29, 2015 1:27 PM ET


Company Overview of Reata Pharmaceuticals, Inc.

Company Overview

Reata Pharmaceuticals, Inc., a clinical-stage biopharmaceutical company, develops drugs for difficult-to-treat diseases. The company develops drugs that target proteins involved in the cellular biology of oxidative stress, inflammation, and mitochondrial function to address the unmet medical needs of patients with serious or life threatening diseases. Its product pipeline comprises drugs under development for treating immuno-oncology and ophthalmology problems, cancers, Friedreich’s ataxia and mitochondrial myopathies, and cardiovascular problems. Reata Pharmaceuticals, Inc. was formerly known as Reata Discovery, Inc. and changed its name to Reata Pharmaceuticals, Inc. in May 2005. The compa...

2801 Gateway Drive

Suite 150

Irving, TX 75063

United States

Founded in 2002





Key Executives for Reata Pharmaceuticals, Inc.

Chairman, Founding Chief Executive Officer and President
Age: 61
Founding Scientist and Scientific Advisor
Founding Scientist and Scientific Advisor
Founding Scientist and Scientific Advisor
Founding Scientist and Scientific Advisor
Compensation as of Fiscal Year 2015.

Reata Pharmaceuticals, Inc. Key Developments

Reata Pharmaceuticals, Inc Receives FDA Clearance for its RTA 744 to Begin Clinical Development

Reata Pharmaceuticals announced that its lead development candidate, RTA 744, has received FDA clearance to begin clinical testing in patients with advanced brain cancers.

Reata Enrolls First Patient in the MOXIe Study

Reata announced enrollment of the first patient in a Phase 2 dose-ranging study examining the safety, tolerability, and efficacy of RTA 408 Oral Capsules versus placebo for the treatment of patients with Friedreich's ataxia. MOXIe (A two-part, randomized, placebo-controlled Phase 2/3 Study of the Safety, Efficacy, and Pharmacodynamics of RTA 408 in the Treatment of Friedreich's Ataxia) is a multi-center study in approximately 52 patients and is designed to support a potential NDA submission. Part 1 of the study is a randomized, placebo-controlled, double-blind, dose-escalation study to evaluate the safety of RTA 408 at 2.5 mg, 5 mg, and 10 mg in patients with Friedreich's ataxia. Part 2 of the study is a randomized, placebo-controlled, double-blind, parallel-group study to evaluate the safety, efficacy, and pharmacodynamics of up to 2 dose levels of RTA 408. The study is designed to evaluate a variety of clinical, and biochemical endpoints, including exercise capacity and quality of life measures.

Reata Pharmaceuticals, Inc. Presents at The Trout Group 's Annual 1x1 Management Access Event, Jan-12-2015

Reata Pharmaceuticals, Inc. Presents at The Trout Group 's Annual 1x1 Management Access Event, Jan-12-2015 . Venue: The Handlery Hotel, 351 Geary Street, Union Square, San Francisco, California, United States.

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