Angiogenically Effective Unit Dose Of FGF And Method Of Administering
Abstract
The present invention provides a unit dose comprising 0.2 μg/kg to 36 μg/kg of a recombinant FGF or an angiogenically active fragment or mutein thereof. Also provided is a pharmaceutical composition comprising an angiogenically effective dose of an FGF or an angiogenically active fragment or mutein thereof, and a pharmaceutically acceptable carrier. Also provided is a method for treating a human patient for coronary artery disease, comprising administering into at least one coronary vessel of said patient a safe and angiogenically effective dose of a recombinant FGF of any of SEQ ID NOS: 1-3, 5, 8-10, or 12-14, or an angiogenically active fragment or mutein thereof.
Claims
exact text as granted — not AI-modified1 . A method for treating a human patient for coronary artery disease, comprising administering into one or more coronary vessels in a human patient in need of treatment for coronary artery disease a therapeutically effective amount of an angiogenically active fragment or angiogenically active mutein of a recombinant fibroblast growth factor (FGF) having the sequence set forth in SEQ ID NO:3, SEQ ID NO:5, SEQ ID NO:8, SEQ ID NO:9, or SEQ ID NO:13.
2 . The method of claim 1 , wherein said therapeutically effective amount administered to said patient is a unit dose of about 0.008 mg to about 6.1 mg of said angiogenically active fragment or angiogenically active mutein of said recombinant FGF.
3 . The method of claim 2 , wherein said therapeutically effective amount administered to said patient is a unit dose of 0.3 mg to 3.5 mg of said angiogenically active fragment or angiogenically active mutein of said recombinant FGF.
4 . The method of claim 1 , comprising administering into one or more coronary vessels of said patient about 0.2 μg/kg to about 36 μg/kg of said angiogenically active fragment or angiogenically active mutein of said recombinant FGF.
5 . The method of claim 4 , comprising administering into one or more coronary vessels of said patient about 0.2 μg/kg to about 2 μg/kg of said angiogenically active fragment or angiogenically active mutein of said recombinant FGF.
6 . The method of claim 4 , comprising administering into one or more coronary vessels of said patient about 2 μg/kg to about 20 μg/kg of said angiogenically active fragment or angiogenically active mutein of said recombinant FGF.
7 . The method of claim 4 , comprising administering into one or more coronary vessels of said patient about 20 μg/kg to about 36 μg/kg of said angiogenically active fragment or angiogenically active mutein of said recombinant FGF.
8 . A method for treating a human patient for coronary artery disease, comprising administering into one or more coronary vessels in a human patient in need of treatment for coronary artery disease a therapeutically effective amount of a recombinant fibroblast growth factor (FGF) having the sequence set forth in SEQ ID NO: 10, 12, or 14 or an angiogenically active fragment or an angiogenically active mutein thereof.
9 . The method of claim 8 , wherein said therapeutically effective amount administered to said patient is a unit dose of about 0.008 mg to about 6.1 mg of said recombinant FGF or said angiogenically active fragment or said angiogenically active mutein thereof.
10 . The method of claim 9 , wherein said therapeutically effective amount administered to said patient is a unit dose of 0.3 mg to 3.5 mg of said recombinant FGF or said angiogenically active fragment or said angiogenically active mutein thereof.
11 . The method of claim 8 , comprising administering into one or more coronary vessels of said patient about 0.2 μg/kg to about 36 μg/kg of said recombinant FGF or said angiogenically active fragment or said angiogenically active mutein thereof.
12 . The method of claim 11 , comprising administering into one or more coronary vessels of said patient about 0.2 μg/kg to about 2 μg/kg of said recombinant FGF or said angiogenically active fragment or said angiogenically active mutein thereof.
13 . The method of claim 11 , comprising administering into one or more coronary vessels of said patient about 2 μg/kg to about 20 μg/kg of said recombinant FGF or said angiogenically active fragment or said angiogenically active mutein thereof.
14 . The method of claim 11 , comprising administering into one or more coronary vessels of said patient about 20 μg/kg to about 36 μg/kg of said recombinant FGF or said angiogenically active fragment or said angiogenically active mutein thereof.
15 . A method for inducing angiogenesis in the heart of a patient, comprising administering into one or more coronary vessels of a human patient in need of coronary angiogenesis a therapeutically effective amount of a recombinant fibroblast growth factor (FGF) having the sequence set forth in SEQ ID NO:3, 5, 10, 12, or 14 or an angiogenically active fragment or an angiogenically active mutein thereof, or a therapeutically effective amount of an angiogenically active fragment or an angiogenically active mutein of a recombinant fibroblast growth factor (FGF) having the sequence set forth in SEQ ID NO:8, SEQ ID NO:9, or SEQ ID NO:13.
16 . The method of claim 15 , wherein said therapeutically effective amount administered to said patient is a unit dose of about 0.008 mg to about 6.1 mg of said recombinant FGF or said angiogenically active fragment or said angiogenically active mutein thereof.
17 . The method of claim 15 , wherein said unit dose is administered into two coronary vessels of said patient.
18 . The method of claim 15 , further comprising the step of administering to said patient an effective amount of a glycosaminoglycan within 30 minutes of administering said recombinant FGF or said angiogenically active fragment or said angiogenically active mutein thereof.
19 - 21 . (canceled)Join the waitlist — get patent alerts
Track US2018221446A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.