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Enanta Pharmaceuticals Inc: Premium Databases

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Enanta Pharmaceuticals Regulatory Milestones

Track drug and patent expiries along with geographies impacted.

A sample of Enanta 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 3 results.
Deserunt mollit sunt Lorem Lorem Lorem Pfizer Inc Lorem WXYZ Lorem Pending Lorem
EDP-305 - - Enanta Pharmaceuticals Inc United States US10080743 Apr-2037 - Phase II
glecaprevir glecaprevir - Enanta Pharmaceuticals Inc Japan JP5857053 Sep-2031 - -
glecaprevir glecaprevir - Enanta Pharmaceuticals Inc United States US8648037 Jan-2032 - -

A sample of Enanta Pharmaceuticals Inc Review Designation data

Drug Name Generic Name Company Name Indication Geography Designation Type Designation Status Designation Date
Showing 3 of 3 results.
Deserunt mollit sunt Lorem laborum do id aliqua dolore Lorem Pfizer Inc Lorem Lorem Lorem Lorem 29 Mar 2022
EDP-514 - Enanta Pharmaceuticals Inc Hepatitis B United States Fast Track Designation Designated 08 Jul 2019
EDP-938 - Enanta Pharmaceuticals Inc Respiratory Syncytial Virus (RSV) Infections United States Fast Track Designation Designated 08 May 2018
EDP-305 - Enanta Pharmaceuticals Inc Non-Alcoholic Steatohepatitis (NASH) United States Fast Track Designation Designated 04 Jan 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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