Developer docs
API playgroundTry for free, no card

Search company profiles

Reata Pharmaceuticals

Full company profile

uuid00049rr

Namestring
Reata Pharmaceuticals
Legal namestring
Reata Pharmaceuticals, Inc.
Websiteurl
reatapharma.com
Company typeenum
Public
Founded yearint
2002
Descriptiontext

Reata Pharmaceuticals is a biopharmaceutical company founded in 2002 and headquartered in Irving, Texas, that developed novel therapeutics for serious diseases with significant unmet medical needs. Its core asset, SKYCLARYS (omaveloxolone), is an oral small molecule that received FDA approval in February 2023 as the first and only treatment for Friedreich's ataxia, a rare progressive neurodegenerative disease affecting coordination, muscle function, and cardiac health. The product was enabled by Reata's proprietary Nrf2 agonist platform, which produced a therapy addressing an indication with no previously approved disease-modifying options in the United States. SKYCLARYS was approved for patients aged 16 and older and distributed through specialty pharmacies serving the rare neurological disease patient population.

The company was publicly traded on NASDAQ under the ticker RETA and operated with 251–500 employees. Beyond SKYCLARYS, Reata had historically pursued bardoxolone methyl for multiple indications, but discontinued its chronic kidney disease (CKD) programs in Q1 2023 following trial results, narrowing strategic focus to the neurology franchise. The company secured a $275 million debt facility in Q1 2023 to extend its cash runway through 2026, providing optionality ahead of its next strategic move.

In July 2023, Biogen Inc. announced a definitive agreement to acquire Reata for $172.50 per share in cash, representing an enterprise value of approximately $7.3 billion. The transaction, which closed in Q3 2023, was motivated by Biogen's intent to expand its rare neurological disease portfolio and was followed by Reata being absorbed into Biogen's operations as a wholly-owned subsidiary.

Short descriptiontext

Reata Pharmaceuticals is a biopharmaceutical company that developed SKYCLARYS, the first FDA-approved treatment for Friedreich's ataxia, using its proprietary Nrf2 agonist platform. Acquired by Biogen in 2023 for approximately $7.3 billion following its February 2023 product launch.

Operating statusenum
Acquired
Ownership categoryenum
Headcount rangeband
251–500
akta.pro rankint
HeadquartersIrving, United States
HQ citystring
Irving
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Keyword5 values
rare disease therapeutics, neurological disease treatments, friedreich ataxia drug, small molecule pharmaceuticals, specialty biopharmaceuticals
Industry4 codes
1Rare Pediatric & Congenital Disorder Therapies
CodeHLAIAIANPrimaryYes
2Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryNo
3Rare Renal & Nephrology Disorder Therapies
CodeHLAIAIAIPrimaryNo
4Nephrology & Urology Pharmaceuticals
CodeHLAIAAAMPrimaryNo
NAICS code2 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Pharmaceutical and Medicine Manufacturing3254
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Rare Disease Therapeutics
Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Supply Chain
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1SKYCLARYS
Description

FDA-approved treatment for Friedreich's ataxia, the first and only treatment for this rare neurological disease in the United States.

biospace.com
Core offering1 text field

Reata Pharmaceuticals developed and commercialized SKYCLARYS (omaveloxolone), the first and only FDA-approved oral treatment for Friedreich's ataxia in patients aged 16 and older in the United States. The company also developed bardoxolone methyl for chronic kidney disease indications, though CKD programs were discontinued in 2023. Reata operated as a specialty biopharmaceutical company focused on novel small molecule therapeutics for serious diseases with significant unmet medical need.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • FDA approval obtained February 2023 for SKYCLARYS
Product overview1 text field

Reata Pharmaceuticals operated as a biopharmaceutical company focused on developing novel therapeutics for severe diseases with significant unmet medical needs. The company's primary product portfolio centered on SKYCLARYS, an FDA-approved oral treatment for Friedreich's ataxia. The company also developed bardoxolone methyl (bardoxolone) for various indications, though CKD programs were discontinued following trial results. Reata Pharmaceuticals was acquired by Biogen in 2023.

Product and service1 record
1SKYCLARYS (omaveloxolone)
CategoryRare disease therapeutics / specialty neurology
Description

SKYCLARYS is an FDA-approved oral small molecule drug for the treatment of Friedreich's ataxia in patients 16 years of age and older. It is the first and only approved therapy specifically for this rare neuromuscular disorder in the United States, addressing a previously unmet medical need.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Recent move5 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight3 records

Each record includes

Type, Description

Peers10 records
TypeEmerging player
Description

Early-stage biotech developing genomic medicines for serious nucleotide-repeat diseases including Friedreich's ataxia. Emerging competitive threat in Reata's primary indication.

TypeBroad incumbent
Description

Established rare disease unit within AstraZeneca with multiple orphan-drug franchises in neurology, hematology, and metabolic disease. Provides broader commercialization scale comparable to Biogen's acquisition rationale for Reata.

TypeDirect peer
Description

Clinical-stage biopharmaceutical company developing treatments specifically for Friedreich's ataxia. Directly competes with SKYCLARYS in the same indication and patient population.

TypeDirect peer
Description

Develops vatiquinone and other candidates for Friedreich's ataxia and other rare neurological/mitochondrial disorders. Directly comparable to Reata in the Friedreich's ataxia competitive landscape.

TypeDirect peer
Description

Specialty biopharma focused exclusively on rare diseases with multiple orphan-drug approvals. Closely aligned with Reata's business model of developing and commercializing treatments for ultra-rare conditions.

TypeDirect peer
Description

Commercial-stage rare disease biotech with multiple approved products across metabolic, neurological, and other orphan indications. Comparable model of single-platform rare disease development and commercialization.

TypeDirect peer
Description

Specialty biopharma focused on rare neuromuscular and neurological genetic diseases with multiple approved RNA-based therapies. Closely aligned with Reata's rare neurodegenerative focus.

TypeDirect peer
Description

Develops RNA-targeted therapeutics for serious and rare neurological, neuromuscular, and metabolic diseases. Comparable specialty pharma approach in rare neurological disorders.

TypeBroad incumbent
Description

Large-cap biopharma with deep rare-disease franchise (cystic fibrosis, sickle cell) and growing rare neurology pipeline. Broader incumbent operating across multiple rare disease verticals.

TypeEmerging player
Description

Specialty biopharma focused on CNS disorders with approved rare-epilepsy therapy. Similar model of small molecule neurology development in underserved indications.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks4 records

Each record includes

Headline, Details, Source

Key highlights3 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment1 record

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature1 record

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds16 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors10 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Reata Pharmaceuticals

Rare Disease Therapeuticsreatapharma.com

Reata Pharmaceuticals is a biopharmaceutical company that developed SKYCLARYS, the first FDA-approved treatment for Friedreich's ataxia, using its proprietary Nrf2 agonist platform. Acquired by Biogen in 2023 for approximately $7.3 billion following its February 2023 product launch.

What Reata Pharmaceuticals does

Reata Pharmaceuticals is a biopharmaceutical company founded in 2002 and headquartered in Irving, Texas, that developed novel therapeutics for serious diseases with significant unmet medical needs. Its core asset, SKYCLARYS (omaveloxolone), is an oral small molecule that received FDA approval in February 2023 as the first and only treatment for Friedreich's ataxia, a rare progressive neurodegenerative disease affecting coordination, muscle function, and cardiac health. The product was enabled by Reata's proprietary Nrf2 agonist platform, which produced a therapy addressing an indication with no previously approved disease-modifying options in the United States. SKYCLARYS was approved for patients aged 16 and older and distributed through specialty pharmacies serving the rare neurological disease patient population.

The company was publicly traded on NASDAQ under the ticker RETA and operated with 251–500 employees. Beyond SKYCLARYS, Reata had historically pursued bardoxolone methyl for multiple indications, but discontinued its chronic kidney disease (CKD) programs in Q1 2023 following trial results, narrowing strategic focus to the neurology franchise. The company secured a $275 million debt facility in Q1 2023 to extend its cash runway through 2026, providing optionality ahead of its next strategic move.

In July 2023, Biogen Inc. announced a definitive agreement to acquire Reata for $172.50 per share in cash, representing an enterprise value of approximately $7.3 billion. The transaction, which closed in Q3 2023, was motivated by Biogen's intent to expand its rare neurological disease portfolio and was followed by Reata being absorbed into Biogen's operations as a wholly-owned subsidiary.

Reata Pharmaceuticals firmographics

Firmographics
Name
Reata Pharmaceuticals
Legal name
Reata Pharmaceuticals, Inc.
Website
https://reatapharma.com
Company type
Public
Founded year
2002
Operating status
Acquired
Headcount range
251–500 employees
Short description
Reata Pharmaceuticals is a biopharmaceutical company that developed SKYCLARYS, the first FDA-approved treatment for Friedreich's ataxia, using its proprietary Nrf2 agonist platform. Acquired by Biogen in 2023 for approximately $7.3 billion following its February 2023 product launch.
Ownership category
akta.pro rank

Reata Pharmaceuticals industry classification

Industry
Product category
Rare Disease Therapeutics
NAICS
Pharmaceutical Preparation Manufacturing (325412), Pharmaceutical and Medicine Manufacturing (3254)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Rare Pediatric & Congenital Disorder Therapies (HLAIAIAN)
akta.pro secondary industries
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC), Rare Renal & Nephrology Disorder Therapies (HLAIAIAI), Nephrology & Urology Pharmaceuticals (HLAIAAAM)

Keywords

  • Rare disease therapeutics
  • Neurological disease treatments
  • Friedreich ataxia drug
  • Small molecule pharmaceuticals
  • Specialty biopharmaceuticals

Where Reata Pharmaceuticals is headquartered

Location

Headquarters

HQ city
Irving
HQ country
United States
HQ region
North America

Markets served

Reata Pharmaceuticals business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales, Supply Chain

Reata Pharmaceuticals product offering

Product offering

Core offering

Reata Pharmaceuticals developed and commercialized SKYCLARYS (omaveloxolone), the first and only FDA-approved oral treatment for Friedreich's ataxia in patients aged 16 and older in the United States. The company also developed bardoxolone methyl for chronic kidney disease indications, though CKD programs were discontinued in 2023. Reata operated as a specialty biopharmaceutical company focused on novel small molecule therapeutics for serious diseases with significant unmet medical need.

Product overview

Reata Pharmaceuticals operated as a biopharmaceutical company focused on developing novel therapeutics for severe diseases with significant unmet medical needs. The company's primary product portfolio centered on SKYCLARYS, an FDA-approved oral treatment for Friedreich's ataxia. The company also developed bardoxolone methyl (bardoxolone) for various indications, though CKD programs were discontinued following trial results. Reata Pharmaceuticals was acquired by Biogen in 2023.

Differentiator

Problem solved

Functional benefit

Brands

  • SKYCLARYS: FDA-approved treatment for Friedreich's ataxia, the first and only treatment for this rare neurological disease in the United States.

Products and services

  • SKYCLARYS (omaveloxolone) SKYCLARYS is an FDA-approved oral small molecule drug for the treatment of Friedreich's ataxia in patients 16 years of age and older. It is the first and only approved therapy specifically for this rare neuromuscular disorder in the United States, addressing a previously unmet medical need.

Quantifiable outcome

  • FDA approval obtained February 2023 for SKYCLARYS

Companies that use Reata Pharmaceuticals

Customer profile

Segments1 record

Ideal customer profiles1 record

Reata Pharmaceuticals technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature1 record

Reata Pharmaceuticals partnerships and signals

Strategic signal

Scale indicators4 records

Recent moves5 records

Expansion highlights3 records

Reata Pharmaceuticals competitors and assessment

Company assessment

Emerging players

  • Design Therapeutics: Early-stage biotech developing genomic medicines for serious nucleotide-repeat diseases including Friedreich's ataxia. Emerging competitive threat in Reata's primary indication.
  • SAGE Therapeutics: Specialty biopharma focused on CNS disorders with approved rare-epilepsy therapy. Similar model of small molecule neurology development in underserved indications.

Broad incumbents

  • Alexion / AstraZeneca Rare Disease: Established rare disease unit within AstraZeneca with multiple orphan-drug franchises in neurology, hematology, and metabolic disease. Provides broader commercialization scale comparable to Biogen's acquisition rationale for Reata.
  • Vertex Pharmaceuticals: Large-cap biopharma with deep rare-disease franchise (cystic fibrosis, sickle cell) and growing rare neurology pipeline. Broader incumbent operating across multiple rare disease verticals.

Direct peers

  • Larimar Therapeutics: Clinical-stage biopharmaceutical company developing treatments specifically for Friedreich's ataxia. Directly competes with SKYCLARYS in the same indication and patient population.
  • PTC Therapeutics: Develops vatiquinone and other candidates for Friedreich's ataxia and other rare neurological/mitochondrial disorders. Directly comparable to Reata in the Friedreich's ataxia competitive landscape.
  • BioMarin Pharmaceutical: Specialty biopharma focused exclusively on rare diseases with multiple orphan-drug approvals. Closely aligned with Reata's business model of developing and commercializing treatments for ultra-rare conditions.
  • Ultragenyx Pharmaceutical: Commercial-stage rare disease biotech with multiple approved products across metabolic, neurological, and other orphan indications. Comparable model of single-platform rare disease development and commercialization.
  • Sarepta Therapeutics: Specialty biopharma focused on rare neuromuscular and neurological genetic diseases with multiple approved RNA-based therapies. Closely aligned with Reata's rare neurodegenerative focus.
  • Ionis Pharmaceuticals: Develops RNA-targeted therapeutics for serious and rare neurological, neuromuscular, and metabolic diseases. Comparable specialty pharma approach in rare neurological disorders.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat3 records

Key risks4 records

Key highlights3 records

Customer concentration

Reata Pharmaceuticals social profiles

Digital presence

Reata Pharmaceuticals financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Reata Pharmaceuticals leadership team

Management profile

Number of profiles

Reata Pharmaceuticals funding detail

Funding detail

Funding overview

Funding rounds16 records

Investors10 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Reata Pharmaceuticals M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Reata Pharmaceuticals

What does Reata Pharmaceuticals do?

Reata Pharmaceuticals developed and commercialized SKYCLARYS (omaveloxolone), the first and only FDA-approved oral treatment for Friedreich's ataxia in patients aged 16 and older in the United States. The company also developed bardoxolone methyl for chronic kidney disease indications, though CKD programs were discontinued in 2023. Reata operated as a specialty biopharmaceutical company focused on novel small molecule therapeutics for serious diseases with significant unmet medical need.

Is Reata Pharmaceuticals a public or private company?

Reata Pharmaceuticals is a public company. It is classified as corporate owned and is currently acquired.

When was Reata Pharmaceuticals founded?

Reata Pharmaceuticals was founded in 2002. It employs 251 to 500 people.

Where is Reata Pharmaceuticals based?

Reata Pharmaceuticals is headquartered in Irving, United States, in the North America region.

Who are Reata Pharmaceuticals's main competitors?

Emerging players on record are Design Therapeutics and SAGE Therapeutics. Broad incumbents are Alexion / AstraZeneca Rare Disease and Vertex Pharmaceuticals. Direct peers are Larimar Therapeutics, PTC Therapeutics, BioMarin Pharmaceutical, Ultragenyx Pharmaceutical, Sarepta Therapeutics and Ionis Pharmaceuticals.

Does Reata Pharmaceuticals have an API?

No public API is recorded for Reata Pharmaceuticals.

What industry is Reata Pharmaceuticals in?

Reata Pharmaceuticals's product category is Rare Disease Therapeutics. Its primary akta.pro industry code is HLAIAIAN, Rare Pediatric & Congenital Disorder Therapies, with a secondary code of HLAIACAC, Neurology & CNS Specialty Pharmaceuticals. Its NAICS code is 325412 and its SIC code is 2834.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
BioPharm InternationalBillions of Reasons to be BuoyantGoldman Sachs forecasts that the pharmaceutical industry possesses approximately $700 billion in cash and leverage, driving expectations for continued mergers and acquisitions to offset impending blockbuster patent expirations. The article highlights strong market performance among specific firms such as Madrigal Pharmaceuticals, Pliant Therapeutics, and Reata Pharmaceuticals due to positive clinical trial results.pharmaphorumLeqembi sales grow again after subcutaneous approvalsBiogen's Q2 results show Leqembi sales rose 15% to $184 million, with $97 million from the US. The growth follows approvals of a subcutaneous version, which Biogen expects to push annual sales above $1 billion. The company also reported gains in other franchises, including Zurzuvae and Empaveli.The Motley FoolBest Healthcare Stocks to Buy in 2026Biogen and Novo Nordisk are compared as healthcare stocks, with Biogen awaiting FDA approval for a subcutaneous Leqembi formulation and Novo Nordisk seeing Wegovy sales rise after pill-form approval. Biogen's shares rose over 13.5% this year, while Novo Nordisk's fell nearly 8%, with Novo Nordisk favored as a better buy.openPR.comMarket Driver Insights: The Impact of Emerging Trends on the Rare Neurological Disease Treatment MarketThe rare neurological disease treatment market is projected to reach $16.05 billion by 2030, growing at a compound annual growth rate of 8.6%, driven by advancements in gene therapies, personalized medicine, increased neurodegenerative research investments, and expanded clinical trials for rare neurological disorders. In February 2024, Harmony Biosciences acquired Epygenix Therapeutics, a clinical-stage company specializing in rare epilepsy therapies, to accelerate development of treatments for Dravet syndrome and Lennox-Gastaut syndrome. Additionally, Reata Pharmaceuticals received FDA approval in February 2023 for Skyclarys, a drug designed to treat Friedreich's ataxia, addressing unmet medical needs in rare neurological conditions.openPR.comAutosomal Dominant Polycystic Kidney Disease Market 2033: Rising Drug Pipeline, Precision Medicine Growth & Lucrative Investment Opportunities in Rare Kidney Disease TherapeuticsDataM Intelligence released a market research report on the Autosomal Dominant Polycystic Kidney Disease (ADPKD) market, which was valued at US$ 1.93 billion in 2024 and is projected to reach US$ 2.83 billion by 2033, growing at a CAGR of 4.4%. Multiple pharmaceutical companies including Otsuka Pharmaceutical, Vertex Pharmaceuticals, Takeda Pharmaceutical, and Astellas Pharma are advancing clinical programs and research initiatives for ADPKD treatments in 2026.openPR.comFriedreich's Ataxia Market Size, Share, Trends, Competitive Landscape, Regional Analysis Forecasts By 2023 |Reata Pharmaceuticals, Inc., Retrotope Inc., MinoryxThe article discusses a market research report on Friedreich's Ataxia scheduled from 2026 to 2033, highlighting the market size, trends, and key players including Reata Pharmaceuticals, Inc., Retrotope Inc., and Minoryx. The report covers segmentation details, regional analysis, and strategic insights for industry stakeholders.GlobeNewswireBiogen Completes Acquisition of Reata PharmaceuticalsBiogen completed its acquisition of Reata Pharmaceuticals, adding SKYCLARYS (omaveloxolone), the first FDA-approved treatment for Friedreich's ataxia in the U.S. The commercial launch is underway, with over 1,000 patient start forms submitted. Biogen expects the deal to be slightly dilutive in 2023, neutral in 2024, and accretive from 2025.Barron'sIntel, Ford, Roku, Reata, Exxon, Enphase, and More Stock Market MoversThe Dow and S&P 500 each gained for a third consecutive week as traders processed earnings reports and economic data. The article lists Intel, Ford, Roku, Reata, Exxon, and Enphase among today's stock market movers.BenzingaDow Surges 250 Points; Exxon Mobil Earnings Miss Expectations - Business First Bancshares (NASDAQ:BFST),U.S. stocks rose mid-week with the Dow Jones gaining approximately 250 points, while Exxon Mobil reported second-quarter earnings that missed analyst expectations due to lower natural gas prices and refining margins. The article also notes significant stock movements for other companies, including a surge in Business First Bancshares shares following strong results and a spike in Reata Pharmaceuticals stock after an acquisition agreement with Biogen.BenzingaWhy Reata Pharmaceuticals (RETA) Stock Is Trading Higher Premarket Today - Biogen (NASDAQ:BIIB)Biogen Inc has agreed to acquire Reata Pharmaceuticals Inc for $172.50 per share in cash, representing an enterprise value of approximately $7.3 billion. Reata's FDA-approved drug Skyclarys is the first and only approved treatment for Friedreich's ataxia in the U.S., with a commercial launch underway and European regulatory review ongoing. The transaction is expected to be slightly dilutive to Biogen's Non-GAAP diluted EPS in 2023, roughly neutral in 2024, and significantly accretive beginning in 2025.