Octapharma AG - Company Profile
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Octapharma AG Regulatory Milestones
Track drug and patent expiries along with geographies impacted.
A sample of Octapharma AG 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 |
|---|---|---|---|---|---|---|---|---|
| Deserunt mollit sunt Lorem | Lorem | Lorem | Pfizer Inc | Lorem | WXYZ | Lorem | Pending | Lorem |
| SubQ-8 | antihemophilic factor (recombinant) | - | Octapharma AG | United States | US10251940 | Sep-2035 | - | - |
| SubQ-8 | antihemophilic factor (recombinant) | - | Octapharma AG | EU | EP3152230 | Jun-2035 | - | - |
| Cutaquig | immune globulin (human) | Cutaquig | Octapharma AG | United States | - | - | Pending | Marketed |
A sample of Octapharma AG Review Designation data
| 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 | 19 Apr 2017 |
| (coagulation factor VII (human) + coagulation factor IX (human) + coagulation factor X + protein C + protein S (human) + prothrombin) | (coagulation factor VII (human) + coagulation factor IX (human) + coagulation factor X + protein C + protein S (human) + prothrombin) | Octapharma AG | Bleeding And Clotting Disorders | United States | Orphan Drug Designation | Designated | 01 Feb 2008 |
| coagulation factor VIII (human) | coagulation factor VIII (human) | Octapharma AG | Hemophilia A (Factor VIII Deficiency) | United States | Orphan Drug Designation | Designated/Withdrawn | 12 Mar 2012 |
| (antihemophilic factor (human) + von willebrand factor complex (human)) | (antihemophilic factor (human) + von willebrand factor complex (human)) | Octapharma USA Inc | Von Willebrand Disease (vWD) | United States | Orphan Drug Designation | Designated/Approved | 18 Apr 2007 |
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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