IP Library Granted Patent US 10,202,446
Granted Patent B2
US 10,202,446 · App. 15/040,103 · Granted Feb 12, 2019

Anti FGF23 antibody and a pharmaceutical composition comprising the same

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Quick Facts
Patent No.
US 10,202,446
App. No.
15/040,103
Granted
Feb 12, 2019
Kind
B2
Abstract

To provide an antibody against FGF23 and a pharmaceutical composition such as a preventive or therapeutic agent which can prevent or treat by suppressing an action of FGF23 by using the antibody. An antibody or its functional fragment against human FGF23 produced by hybridoma C10 (Accession No. FERM BP-10772).

Claims (8)

1. A method for treating a hypophosphatemic disease characterized by elevated FGF23 concentrations compared to that observed in healthy subjects, comprising administering an antibody or functional fragment thereof to a subject in need thereof, wherein the antibody or functional fragment thereof binds to FGF23 and comprises:

(a) a heavy chain comprising a CDR1 sequence of SEQ ID NO: 40, a CDR2 sequence of SEQ ID NO: 41, and a CDR3 sequence of SEQ ID NO: 42; and

(b) a light chain comprising a CDR1 sequence of SEQ ID NO: 43, a CDR2 sequence of SEQ ID NO: 44, and a CDR3 sequence of SEQ ID NO: 45.

2. The method of claim 1 , wherein the disease is selected from the group consisting of tumor-induced osteomalacia, ADHR, XLH, fibrous dysplasia, and McCune-Albright syndrome.

3. A method for increasing serum phosphorous concentration in a subject suffering from a hypophosphatemic disease characterized by elevated FGF23 concentrations compared to that observed in healthy subjects, comprising administering an antibody or functional fragment thereof to the subject, wherein the antibody or functional fragment thereof binds to FGF23 and comprises:

(a) a heavy chain comprising a CDR1 sequence of SEQ ID NO: 40, a CDR2 sequence of SEQ ID NO: 41, and a CDR3 sequence of SEQ ID NO: 42; and

(b) a light chain comprising a CDR1 sequence of SEQ ID NO: 43, a CDR2 sequence of SEQ ID NO: 44, and a CDR3 sequence of SEQ ID NO: 45.

4. The method of claim 3 , wherein the disease is selected from the group consisting of tumor-induced osteomalacia, ADHR, XLH, fibrous dysplasia, and McCune-Albright syndrome.

Assignments (1)
CHANGE OF NAME Recorded Sep 16, 2019
From: KYOWA HAKKO KIRIN CO., LTD.
To: KYOWA KIRIN CO., LTD.
Reel/Frame 050385/0075 →