Track drug and patent expiries along with geographies impacted.
|Drug Name||Generic Name||Brand Name||Company Name||Expiry Geography||Constraining Patent Number||Constraining Patent Expiry||Drug Expiry (Estimated)||Highest Development Stage|
|Deserunt mollit sunt Lorem||Lorem||Lorem||Pfizer Inc||Lorem||XXXX||Lorem||Pending||Lorem|
|Opzelura||ruxolitinib phosphate||Opzelura||Incyte Corp||Japan||JP5849312||May-2031||-||-|
|Opzelura||ruxolitinib phosphate||Opzelura||Incyte Corp||EU||EP2574168||May-2031||-||Pre-Registration|
|INCA-00186||-||-||Incyte Corp||United States||US20210230293||-||Pending||-|
|Drug Name||Generic Name||Company Name||Indication||Geography||Designation Type||Designation Status||Designation Date|
|Deserunt mollit sunt Lorem laborum do id aliqua dolore||Lorem||Pfizer Inc||Lorem||Lorem||Lorem||Lorem||20 Jun 2022|
|Opzelura||ruxolitinib phosphate||Incyte Corp||Atopic Dermatitis (Atopic Eczema)||United States||Priority Review||Designated/Approved||19 Feb 2021|
|INCB-00928||-||Incyte Corp||Fibrodysplasia Ossificans Progressiva (Myositis Ossificans Progressiva)||United States||Orphan Drug Designation||Designated||21 Jul 2020|
|INCB-00928||-||Incyte Corp||Fibrodysplasia Ossificans Progressiva (Myositis Ossificans Progressiva)||United States||Fast Track Designation||Designated||-|
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.
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).
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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