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Fate Therapeutics Inc: Premium Databases

Fate Therapeutics Regulatory Milestones

Track drug and patent expiries along with geographies impacted.

A sample of Fate Therapeutics 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
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Deserunt mollit sunt Lorem Lorem Lorem Pfizer Inc Lorem XXXX Lorem Pending Lorem
FT-576 - - Fate Therapeutics Inc United States US10927346 Dec-2038 - Phase I
FT-596 - - Fate Therapeutics Inc Japan JP5793795 Dec-2029 - -
FT-596 - - Fate Therapeutics Inc United States US8044201 Dec-2029 - Phase I

A sample of Fate Therapeutics Inc Review Designation data

Drug Name Generic Name Company Name Indication Geography Designation Type Designation Status Designation Date
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Deserunt mollit sunt Lorem laborum do id aliqua dolore Lorem Pfizer Inc Lorem Lorem Lorem Lorem 13 Dec 2021
ProTmune - Fate Therapeutics Inc Hematopoietic Stem Cell Transplantation EU Orphan Drug Designation Designated 18 Nov 2016
ProTmune - Fate Therapeutics Inc Graft Versus Host Disease (GVHD) EU Orphan Drug Designation Designated 31 Oct 2016
ProTmune - Fate Therapeutics Inc Graft Versus Host Disease (GVHD) United States Orphan Drug Designation Designated 19 Sep 2016
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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