Eisai Co Ltd - Company Profile

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Eisai Regulatory Milestones

Track drug and patent expiries along with geographies impacted.

A sample of Eisai 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 30+ results.
Deserunt mollit sunt Lorem Lorem Lorem Pfizer Inc Lorem WXYZ Lorem Pending Lorem
E-7766 - - Eisai Co Ltd United States US10246480 Feb-2038 - Phase I
E-7766 - - Eisai Co Ltd EU EP3582853 Feb-2038 - Phase I
E-7130 - - Eisai Co Ltd Japan JP6366873 Apr-2038 - Phase I

A sample of Eisai Co Ltd Review Designation data

Drug Name Generic Name Company Name Indication Geography Designation Type Designation Status Designation Date
Showing 3 of 30+ results.
Deserunt mollit sunt Lorem laborum do id aliqua dolore Lorem Pfizer Inc Lorem Lorem Lorem Lorem 05 Jul 2022
H-3B6527 - H3 Biomedicine Inc Hepatocellular Carcinoma EU Orphan Drug Designation Designated 23 Aug 2017
RVT-2001 - H3 Biomedicine Inc Acute Myelocytic Leukemia (AML, Acute Myeloblastic Leukemia) United States Orphan Drug Designation Designated 21 Jun 2017
tasurgratinib tasurgratinib [INN] Eisai Co Ltd Bile Duct Cancer (Cholangiocarcinoma) Japan Orphan Drug Designation Designated 22 Feb 2021
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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