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|
|(abacavir sulfate + dolutegravir sodium+ lamivudine) ODT||(abacavir sulfate + dolutegravir sodium + lamivudine)||Triumeq PD||GSK plc||Japan||JP4295353||Apr-2031||-||-|
|(abacavir sulfate + dolutegravir sodium+ lamivudine) ODT||(abacavir sulfate + dolutegravir sodium + lamivudine)||Triumeq PD||GSK plc||EU||EP1874117||Jan-2029||-||-|
|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||01 Dec 2018|
|dolutegravir sodium ODT||dolutegravir sodium||ViiV Healthcare Company||Human Immunodeficiency Virus (HIV) Infections (AIDS)||United States||Priority Review||Designated/Approved||-|
|cabotegravir sodium||cabotegravir sodium||ViiV Healthcare Company||Human Immunodeficiency Virus (HIV) Infections (AIDS)||United States||Fast Track Designation||Designated/Approved||-|
|cabotegravir sodium||cabotegravir sodium||ViiV Healthcare Company||Human Immunodeficiency Virus (HIV) Infections (AIDS)||United States||Priority Review||Designated/Approved||-|
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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