Search Orphan Drug Designations and Approvals
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| Generic Name: | antihemophilic factor (recombinant), Fc fusion protein | ||||||||||||||||
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| Trade Name: | Eloctate | ||||||||||||||||
| Date Designated: | 11/23/2010 | ||||||||||||||||
| Orphan Designation: | Treatment of hemophilia A | ||||||||||||||||
| Orphan Designation Status: | Designated/Approved | ||||||||||||||||
| Sponsor: |
Bioverativ Therapeutics, Inc. 225 2nd Avenue Waltham, Massachusetts 02451 United States The sponsor address listed is the last reported by the sponsor to OOPD. |
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Marketing approved: |
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| 1 | Generic Name: | antihemophilic factor (recombinant), Fc fusion protein |
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| Trade Name: | Eloctate | |
| Marketing Approval Date: | 06/06/2014 | |
| Approved Labeled Indication: | Indicated in adults and children with Hemophilia A (congenital Factor VIII deficiency) for on-demand treatment and control of bleeding episodes, perioperative management of bleeding, and routine prophylaxis to reduce the frequency of bleeding episodes. | |
| Exclusivity End Date: | 06/06/2021 | |
| Exclusivity Protected Indication* : | Treatment of adults and children with Hemophilia A (congenital Factor VIII deficiency) for control and prevention of bleeding episodes, perioperative management, and routine prophylaxis to prevent or reduce the frequency of bleeding episodes. | |
*Data for the Date Designation Withdrawn or Revoked field are shown for designations withdrawn or revoked after 08/12/2013.
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