Daiichi Sankyo Co Ltd - Company Profile

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Daiichi Sankyo Co Ltd: Premium Databases

Daiichi Sankyo Regulatory Milestones

Track drug and patent expiries along with geographies impacted.

A sample of Daiichi Sankyo 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 40+ results.
Deserunt mollit sunt Lorem Lorem Lorem Pfizer Inc Lorem WXYZ Lorem Pending Lorem
DS-8190a - - Daiichi Sankyo Co Ltd EU EP2862861 Jun-2033 - -
DS-2325a - - Daiichi Sankyo Co Ltd Japan JP6888175 Nov-2039 - -
DS-2325a - - Daiichi Sankyo Co Ltd United States US11292828 Nov-2039 - Phase I

A sample of Daiichi Sankyo Co Ltd Review Designation data

Drug Name Generic Name Company Name Indication Geography Designation Type Designation Status Designation Date
Showing 3 of 40+ results.
Deserunt mollit sunt Lorem laborum do id aliqua dolore Lorem Pfizer Inc Lorem Lorem Lorem Lorem 24 Feb 2022
DS-1211 - Daiichi Sankyo Co Ltd Pseudoxanthoma Elasticum (PXE or Gronblad Strandberg Syndrome) EU Orphan Drug Designation Designated -
GEM-ONJ - American Regent Inc Osteonecrosis United States Orphan Drug Designation Designated 01 Feb 2007
phenylephrine hydrochloride phenylephrine hydrochloride American Regent Inc Tetralogy Of Fallot United States Orphan Drug Designation Designated 31 Jan 2012
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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