H. Lundbeck AS - Company Profile

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H. Lundbeck AS: Premium Databases

H. Lundbeck AS Regulatory Milestones

Track drug and patent expiries along with geographies impacted.

A sample of H. Lundbeck 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 14+ results.
Deserunt mollit sunt Lorem Lorem Lorem Pfizer Inc Lorem WXYZ Lorem Pending Lorem
ABD-1970 - - H. Lundbeck AS United States US9771341 Mar-2036 - -
LuAF-87908 - - H. Lundbeck AS Japan JP6878395 Jul-2036 - -
LuAF-87908 - - H. Lundbeck AS United States US10196439 Jul-2036 - -

A sample of H. Lundbeck AS Review Designation data

Drug Name Generic Name Company Name Indication Geography Designation Type Designation Status Designation Date
Showing 3 of 14+ results.
Deserunt mollit sunt Lorem laborum do id aliqua dolore Lorem Pfizer Inc Lorem Lorem Lorem Lorem 20 May 2021
LuAF-82422 - H. Lundbeck AS Multiple System Atrophy (MSA or Shy-Drager Syndrome or Multi-System Degeneration) EU Orphan Drug Designation Designated 20 May 2021
eptinezumab eptinezumab-jjmr H. Lundbeck AS Migraine United States Standard Review Designated/Approved 22 Apr 2019
vigabatrin vigabatrin Sanofi KK Infantile Spasm (West Syndrome) Japan Orphan Drug Designation Designated/Approved 17 Sep 2014
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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