IP Library Granted Patent US 11,639,381
Granted Patent B2
US 11,639,381 · App. 16/793,208 · Granted May 2, 2023

Treatment of headache using anti-CGRP antibodies

Inventors: Roger K. Cady (Bothell, WA); Jeffrey T. L. Smith (Dublin, IE); Joseph Hirman (Bothell, WA); Barbara Schaeffler (Bothell, WA); Lahar Mehta (Valby, DK)
Assignee: H. LUNDBECK A/S
C07K16/18A61K9/0019A61K31/4172A61K39/3955A61K45/06A61K47/26A61P25/06A61K38/00A61K2039/505A61K2039/545C07K2317/24
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Quick Facts
Patent No.
US 11,639,381
App. No.
16/793,208
Granted
May 2, 2023
Kind
B2
Abstract

Methods for immediate relief of migraine or headache are provided comprising the administration of an anti-CGRP antagonist antibody to a patient in need thereof.

Claims (15)

1. A method of immediate treatment and relief of migraine headache, comprising intravenously administering to a patient in need thereof an effective amount of an anti-Calcitonin Gene Related Peptide (CGRP) antibody while the patient is experiencing a headache associated with an attack of migraine, wherein said anti-CGRP antibody is a full-length IgG antibody which comprises: the light chain complementarity determining region (CDR) 1, 2, and 3 polypeptide sequences of SEQ ID NO: 224, SEQ ID NO: 226, and SEQ ID NO: 228, respectively; and heavy chain CDR 1, 2, and 3 polypeptide sequences of SEQ ID NO: 204, SEQ ID NO: 206, and SEQ ID NO: 208, respectively; wherein the intravenous administration begins within 1-6 hours of the onset of said migraine headache.

2. The method of claim 1 , wherein the intravenously administered amount of said anti-CGRP antibody is between about 100 mg and about 300 mg.

3. The method of claim 1 , wherein the intravenously administered amount of said anti-CGRP antibody is about 100 mg.

4. The method of claim 1 , wherein the intravenously administered amount of said anti-CGRP antibody is about 300 mg.

5. The method of claim 1 , wherein said anti-CGRP antibody comprises the variable light chain polypeptide of SEQ ID NO: 222 and the variable heavy chain polypeptide of SEQ ID NO: 202.

6. The method of claim 1 , wherein said anti-CGRP antibody comprises the light chain polypeptide of SEQ ID NO: 221 and the heavy chain polypeptide of SEQ ID NO: 201.

7. The method of claim 3 , wherein said anti-CGRP antibody comprises the light chain polypeptide of SEQ ID NO: 221 and the heavy chain polypeptide of SEQ ID NO: 201.

8. A method for treatment of migraine in a patient in the need of rapid relief of migraine, comprising intravenously administering to a patient in need thereof 100 or 300 mg of an anti-Calcitonin Gene Related Peptide (CGRP) antibody while the patient is exhibiting headache and at least one migraine symptom during a migraine attack, wherein said anti-CGRP antibody is a full-length IgG antibody which comprises: the light chain complementarity determining region (CDR) 1, 2, and 3 polypeptide sequences of SEQ ID NO: 224, SEQ ID NO: 226, and SEQ ID NO: 228, respectively; and heavy chain CDR 1, 2, and 3 polypeptide sequences of SEQ ID NO: 204, SEQ ID NO: 206, and SEQ ID NO: 208, respectively; wherein the intravenous administration begins between 1-6 hours after the onset of said migraine attack.

9. The method of claim 8 , wherein the intravenously administered amount of said anti-CGRP antibody is 100 mg.

10. The method of claim 8 , wherein the intravenously administered amount of said anti-CGRP antibody is 300 mg.

11. The method of claim 8 , wherein the at least one migraine symptom comprises a most bothersome symptom selected from nausea, photophobia, and phonophobia, and wherein the most bothersome symptom is alleviated within 12 hours, within 6 hours, within 5 hours, within 4 hours, within 3 hours, within 2 hours, within 1 hour, or within 30 minutes after the administering.

12. The method of claim 8 , wherein said anti-CGRP antibody comprises the variable light chain polypeptide of SEQ ID NO: 222 and the variable heavy chain polypeptide of SEQ ID NO: 202.

13. The method of claim 8 , wherein said anti-CGRP antibody comprises the light chain polypeptide of SEQ ID NO: 221 and the heavy chain polypeptide of SEQ ID NO: 201.

14. The method of claim 9 , wherein said anti-CGRP antibody comprises the light chain polypeptide of SEQ ID NO: 221 and the heavy chain polypeptide of SEQ ID NO: 201.

15. The method of claim 10 , wherein said anti-CGRP antibody comprises the light chain polypeptide of SEQ ID NO: 221 and the heavy chain polypeptide of SEQ ID NO: 201.

Continuity (5)
Continuation In Part PCTUS2020012781 · Jan 8, 2020
Provisional Application 62789828 · Jan 8, 2019
Provisional Application 62872989 · Jul 11, 2019
Provisional Application 62842162 · May 2, 2019
Related Publication 20200299368A1 · Sep 24, 2020
Cited By (6)
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