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Mesoblast Ltd: Premium Databases

Mesoblast Ltd Regulatory Milestones

Track drug and patent expiries along with geographies impacted.

A sample of Mesoblast Ltd 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
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Deserunt mollit sunt Lorem Lorem Lorem Pfizer Inc Lorem XXXX Lorem Pending Lorem
MPC-75IA - - Mesoblast Ltd United States US9050178 Apr-2021 - -
MPC-75IA - - Mesoblast Ltd EU EP1276486 Apr-2021 - -
MPC-25IC rexlemestrocel-L - Mesoblast Ltd Japan JP5721302 Mar-2024 - -

A sample of Mesoblast Ltd Review Designation data

Drug Name Generic Name Company Name Indication Geography Designation Type Designation Status Designation Date
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Deserunt mollit sunt Lorem laborum do id aliqua dolore Lorem Pfizer Inc Lorem Lorem Lorem Lorem 02 Dec 2020
MPC-CBE - Mesoblast Ltd Bone Marrow Transplant Rejection United States Orphan Drug Designation Designated 12 Sep 2008
rexlemestrocel-L rexlemestrocel-L Mesoblast Ltd Left Ventricular Dysfunction United States Orphan Drug Designation Designated 19 Jun 2019
rexlemestrocel-L rexlemestrocel-L Mesoblast Ltd Left Ventricular Dysfunction United States Regenerative Medicine Advanced Therapy Designation (RMAT) Designated 21 Dec 2017
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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