Changing the landscape in
Life-Threatening Diseases

At Reata Pharmaceuticals, our mission is to develop innovative therapies that change patients’ lives for the better.

Our Pipeline

Reata’s development programs have created a robust pipeline of drug candidates for the treatment of serious, life-threatening diseases. Find out more here.

Pipeline
Phase 1
Phase 2
Pivotal
Regulatory Review
Commerciala
Neurology
Friedreich's Ataxia | Omaveloxolone Friedreich's Ataxia
Omaveloxolone
DPNPb | RTA 901 DPNPb
RTA 901
Chronic Kidney Disease
CKDc Caused by ADPKDd | Bardoxolonee CKDc Caused by ADPKDd
Bardoxolonee
CKD Caused by Alport Syndrome | Bardoxolone CKD Caused by Alport Syndrome
Bardoxolone
Type 1 and Type 2 Diabetes and Advanced CKD | Bardoxolonef Type 1 and Type 2 Diabetes
and Advanced CKD
Bardoxolonef

aOmaveloxolone is approved by the US FDA. bDiabetic peripheral neuropathic pain (DPNP). cChronic Kidney Disease (CKD). dAutosomal Dominant Polycystic Kidney Disease (ADPKD). eBardoxolone methyl (bardoxolone). On February 25, 2022, we received a Complete Response Letter from the Food and Drug Administration (FDA). We will continue to work with the FDA to confirm our next steps on our Alport syndrome program. fAYAME study conducted in Japan by our strategic collaborator in CKD, Kyowa Kirin.

Omaveloxolone is an investigational drug not approved by any other regulatory authority. Bardoxolone methyl, and RTA 901 are investigational drugs. Safety and efficacy have not been established by any agency.

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Dawn of a New Era