Genmab AS - Company Profile

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Genmab AS Regulatory Milestones

Track drug and patent expiries along with geographies impacted.

A sample of Genmab AS 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 9 results.
Deserunt mollit sunt Lorem Lorem Lorem Pfizer Inc Lorem WXYZ Lorem Pending Lorem
epcoritamab epcoritamab - Genmab AS Japan JP6853176 Jan-2036 - Pre-Registration
epcoritamab epcoritamab - Genmab AS United States US10544220 Oct-2035 - Pre-Registration
GEN-1029 - - Genmab AS Japan JP6457386 Jul-2033 - -

A sample of Genmab AS Review Designation data

Drug Name Generic Name Company Name Indication Geography Designation Type Designation Status Designation Date
Showing 3 of 9 results.
Deserunt mollit sunt Lorem laborum do id aliqua dolore Lorem Pfizer Inc Lorem Lorem Lorem Lorem 21 Nov 2022
epcoritamab epcoritamab AbbVie Inc Follicular Lymphoma EU Orphan Drug Designation Designated 21 Jun 2022
epcoritamab epcoritamab Genmab AS Follicular Lymphoma United States Orphan Drug Designation Designated 01 Mar 2022
epcoritamab epcoritamab AbbVie Inc Diffuse Large B-Cell Lymphoma EU Orphan Drug Designation Designated 24 Feb 2022
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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