Chiesi Farmaceutici SpA - Company Profile

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Chiesi Farmaceutici SpA: Premium Databases

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Chiesi Farmaceutici SpA Regulatory Milestones

Track drug and patent expiries along with geographies impacted.

A sample of Chiesi Farmaceutici SpA 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 18+ results.
Deserunt mollit sunt Lorem Lorem Lorem Pfizer Inc Lorem WXYZ Lorem Pending Lorem
budsurf - - Chiesi Farmaceutici SpA United States US8048043 Jan-2030 - -
budsurf - - Chiesi Farmaceutici SpA EU EP2164504 May-2028 - -
CHF-6467 - - Chiesi Farmaceutici SpA United States US20210079053 - Pending -

A sample of Chiesi Farmaceutici SpA Review Designation data

Drug Name Generic Name Company Name Indication Geography Designation Type Designation Status Designation Date
Showing 3 of 18+ results.
Deserunt mollit sunt Lorem laborum do id aliqua dolore Lorem Pfizer Inc Lorem Lorem Lorem Lorem 25 May 2022
Gene Therapy to Activate LAMB-3 for Junctional Epidermolysis Bullosa - Chiesi Farmaceutici SpA Epidermolysis Bullosa EU Orphan Drug Designation Designated 19 Mar 2015
HOLOGENE-17 - Chiesi Farmaceutici SpA Epidermolysis Bullosa EU Orphan Drug Designation Designated 19 Mar 2015
Small Molecule for Cystic Fibrosis - Chiesi Farmaceutici SpA Cystic Fibrosis EU Orphan Drug Designation Designated 22 Feb 2018
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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