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Reata Pharmaceuticals Inc: Premium Databases

Reata Pharmaceuticals Regulatory Milestones

Track drug and patent expiries along with geographies impacted.

A sample of Reata Pharmaceuticals Regulatory Milestones data

Drug Name Generic Name Brand Name Company Name Expiry Geography Constraining Patent Number Constraining Patent Expiry Drug Expiry (Estimated) Highest Development Stage
Showing 3 of 4 results.
Deserunt mollit sunt Lorem Lorem Lorem Pfizer Inc Lorem WXYZ Lorem Pending Lorem
RTA-1701 - - Reata Pharmaceuticals Inc United States US20200131148 - Pending -
RTA-901 - - Reata Pharmaceuticals Inc Japan JP6121450 Feb-2033 - -
RTA-901 - - Reata Pharmaceuticals Inc United States US9422320 Feb-2033 - -

A sample of Reata Pharmaceuticals Inc Review Designation data

Drug Name Generic Name Company Name Indication Geography Designation Type Designation Status Designation Date
Showing 3 of 4 results.
Deserunt mollit sunt Lorem laborum do id aliqua dolore Lorem Pfizer Inc Lorem Lorem Lorem Lorem 26 May 2022
omaveloxolone omaveloxolone [INN] Reata Pharmaceuticals Inc Friedreich Ataxia United States Fast Track Designation Designated 18 Nov 2021
omaveloxolone omaveloxolone [INN] Reata Pharmaceuticals Inc Friedreich Ataxia EU Orphan Drug Designation Designated 27 Jun 2018
omaveloxolone omaveloxolone [INN] Reata Pharmaceuticals Inc Metastatic Melanoma United States Orphan Drug Designation Designated 05 Sep 2017
Regulatory Milestones

Feature

Regulatory Milestones provides an interactive, comprehensive, and analytical view of Drug and Constraining Patent Expiry and Exclusivity for Marketed and Pipeline (till preclinical development stage) pharmaceutical drugs in the United States (US), Europe (United Kingdom, Germany, France, Italy, and Spain) and Japan.

Benefit

Regulatory Milestones provides patent information for all novel Marketed and Pipeline pharmaceutical drugs available in the US, Europe (United Kingdom, Germany, France, Italy, and Spain) and Japan.

The Drug Expiry filters include Expiry Geography and Expiry Date as well as US-specific information.

The Drug Expiry date is based on the Constraining Patent Expiry, Patent Term Extension or Supplementary Protection Certificate (depending on the regulator), Exclusivity analysis and specific information on Review Designations granted by regulators.

US-specific information includes Exclusivity Type and Paragraph IV Certification filing under the Hatch Waxman Act (Paragraph IV).

Value

Regulatory Milestones is easily accessible and features a user-friendly platform. The tool includes attributes relating to Drug Expiry and Constraining Patents as well as attributes from Drugs and Companies .

Clients can utilize Regulatory Milestones to save time and effort through accumulated expiry information from various sources and registries in a standardized comparable format.

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