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  • SOLUTION;INTRAVENOUS - 250MG/50ML (5MG/ML)
  • SOLUTION;INTRAVENOUS - 500MG/100ML (5MG/ML)
  • INJECTABLE;INTRAVENOUS - 250MG/VIAL

Details:

Angiomax-Generic (bivalirudin) is a direct thrombin inhibitor, which is now launched in the US market. It is indicated for treatment of patients with heparin-induced thrombocytopenia and heparin-induced thrombocytopenia and thrombosis syndrome.


Lead Product(s): Bivalirudin

Therapeutic Area: Hematology Product Name: Angiomax-Generic

Highest Development Status: ApprovedProduct Type: Peptide

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 29, 2024

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Details:

Bivalirudin injection in a ready-to-use 250 mg/50 mL single-use vial. It is the only ready-to-use liquid format of bivalirudin on the market in the U.S.


Lead Product(s): Bivalirudin

Therapeutic Area: Hematology Product Name: Angiomax RTU

Highest Development Status: ApprovedProduct Type: Peptide

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 18, 2023

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Details:

The agreement aims to distribute Angiomax RTU (bivalirudin) injection, a direct thrombin inhibitor used to prevent blood clots in people with severe chest pain or other conditions who are undergoing a procedure called angioplasty, in the U.S.


Lead Product(s): Bivalirudin

Therapeutic Area: Hematology Product Name: Angiomax RTU

Highest Development Status: ApprovedProduct Type: Peptide

Partner/Sponsor/Collaborator: MAIA Biotechnology

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Agreement May 24, 2023

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