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    Reata Pharmaceuticals Inc.

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    $RETA
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Reata Pharmaceuticals, Inc., a clinical stage biopharmaceutical company, develops novel therapeutics for patients with serious or life-threatening diseases by targeting molecular pathways that regulate cellular metabolism and inflammation. The company is developing Phase III clinical trial programs, including bardoxolone methyl (bardoxolone) for the treatment of patients with chronic kidney disease (CKD) caused by Alport syndrome, as well as for a form of pulmonary arterial hypertension associated with connective tissue disease; omaveloxolone that is Phase II clinical trial to treat Friedreich's ataxia; and conduct Phase II study for various form of CKD, such as IgA nephropathy, type 1 and type 2 diabetic CKD, hypertensive CKD, focal segmental glomerulosclerosis, and others. It is also developing RTA 901 for neurological diseases; and RTA 1701 for the potential treatment of a range of autoimmune, inflammatory, and fibrotic diseases. In addition, the company offers bardoxolone for the treatment of autosomal dominant polycystic kidney disease. Further, it has a strategic collaboration agreement with Kyowa Kirin Co., Ltd. to develop and commercialize bardoxolone for renal, cardiovascular, diabetes, and various other related metabolic indications in Japan, China, Hong Kong, Macao, South Korea, Taiwan, Thailand, Singapore, the Philippines, Malaysia, Indonesia, Brunei, Vietnam, Laos, Myanmar, and Cambodia; and AbbVie Inc. to jointly research, develop, and commercialize all second- and later-generation Nrf2 activators for all indications other than renal, cardiovascular, and metabolic indications. The company was formerly known as Reata Discovery, Inc. and changed its name to Reata Pharmaceuticals, Inc. in May 2005. Reata Pharmaceuticals, Inc. was incorporated in 2002 and is headquartered in Plano, Texas.

    IPO Year: 2016

    Exchange: NASDAQ

    Website: reatapharma.com

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    Recent Analyst Ratings for Reata Pharmaceuticals Inc.

    DatePrice TargetRatingAnalyst
    7/6/2023$140.00Outperform
    TD Cowen
    6/12/2023$80.00 → $115.00Market Perform → Outperform
    SVB Securities
    10/19/2022$75.00Buy
    Guggenheim
    3/24/2022$91.00Buy
    Goldman
    3/1/2022$39.00 → $34.00Neutral
    Goldman Sachs
    12/9/2021$39.00Buy → Neutral
    Goldman Sachs
    12/9/2021$110.00 → $37.00Outperform → Neutral
    Robert W. Baird
    12/9/2021$112.00 → $68.00Overweight
    Cantor Fitzgerald
    12/9/2021$180.00 → $43.00Overweight
    Barclays
    12/9/2021$282.00 → $35.00Outperform → Market Perform
    SVB Leerink
    See more ratings

    Reata Pharmaceuticals Inc. FDA approvals

    Live FDA approvals issued by the Food and Drug Administration and FDA breaking news

    See more
    • FDA Approval for SKYCLARYS issued to REATA PHARMACEUTICALS INC

      Submission status for REATA PHARMACEUTICALS INC's drug SKYCLARYS (ORIG-1) with active ingredient OMAVELOXOLONE has changed to 'Approval' on 02/28/2023. Application Category: NDA, Application Number: 216718, Application Classification: Type 1 - New Molecular Entity

      2/28/23 5:14:09 PM ET
      $RETA
      Biotechnology: Pharmaceutical Preparations
      Health Care