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Founded in 2002, Reata Pharmaceuticals,
Inc. is a biopharmaceutical company focused on translating
innovative science into breakthrough medicines for intractable
diseases. Reata is the leader in developing oral anti-inflammatory drugs targeting Nrf2, which
controls the body’s production of antioxidants and has been shown
to protect against a broad range of diseases associated with
inflammation and oxidative stress.
The company’s lead program, bardoxolone methyl, is an Antioxidant Inflammation Modulator (AIM) targeting Nrf2 that has been shown to
significantly increase estimated glomerular filtration rate and improve
several other markers of kidney function in patients with chronic kidney disease.
Bardoxolone methyl has been advanced to late-stage,
pivotal clinical trials in patients with chronic kidney disease
and type 2 diabetes mellitus. Chronic kidney disease is a common complication of diabetes and hypertension that affects over 26 million Americans. It is a progressive condition that ultimately leads to the need for dialysis or transplant and is also associated with a dramatic increase in the risk of cardiovascular disease, and represents an area of significant unmet medical need.
Behind this lead program, Reata is developing a portfolio of
other AIMs for additional diseases of inflammation and oxidative
stress. A large body of literature, including over 130 peer-reviewed
articles, has demonstrated the efficacy of Reata’s AIMs in the
treatment of autoimmune diseases (rheumatoid arthritis, multiple
sclerosis, IB); respiratory diseases (COPD, asthma, cystic
fibrosis); CNS diseases (Alzheimer’s, Parkinson’s); and
transplants (graft vs. host disease), as well as the renal,
cardiovascular, and metabolic diseases for which bardoxolone
methyl is being developed.
Several principles drive Reata’s
development approach:
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Selecting superior
translational research projects initiated at leading
research institutions that involve novel biology with the
potential to address intractable diseases. |
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Advancing
preclinical and clinical candidates by applying biological
insights and funding prudently to advance candidates as
quickly and effectively as possible. |
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Selecting optimal
clinical applications in which trials will be manageable in
size and duration, there are well-established endpoints for
pivotal studies, and there is a high regulatory imperative
to approve new therapeutics. |
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