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Integrilin-Generic (eptifibatide) is a USFDA approved platelet aggregation inhibitor, which is indicated for the treatment of patients with acute coronary syndrome.


Lead Product(s): Eptifibatide

Therapeutic Area: Cardiology/Vascular Diseases Product Name: Integrilin-Generic

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 29, 2024

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The company launched desmopressin acetate for injection in the United States as a therapeutic equivalent generic for DDAVP for treating is multi-indicated for patients with central diabetes insipidus, hemophilia A, and von willebrand’s disease (Type I).


Lead Product(s): Desmopressin Acetate

Therapeutic Area: Rare Diseases and Disorders Product Name: DDAVP-Generic

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 15, 2024

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Lasix-Generic (furosemide) is a USFDA approved loop diuretic, which is indicated for the treatment of adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome.


Lead Product(s): Furosemide

Therapeutic Area: Cardiology/Vascular Diseases Product Name: Lasix-Generic

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 20, 2024

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Emend-Generic(fosaprepitant) is a NK1 receptor antagonist, indicated in adults and pediatric patients aged 6 months & older along with other antiemetic agents, for the prevention of acute & delayed nausea & vomiting associated with initial & repeat courses of chemotherapy.


Lead Product(s): Fosaprepitant

Therapeutic Area: Gastroenterology Product Name: Emend-Generic

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 18, 2024

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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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Alkeran-Generic (melphalan hydrochloride) is a DNA alkylating agent of the bischloroethylamine type. It is approved for the treatment of patients with multiple myeloma for whom oral therapy is not appropriate.


Lead Product(s): Melphalan Hydrochloride

Therapeutic Area: Oncology Product Name: Alkeran-Generic

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 16, 2024

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