IP Library › Granted Patent US 11,123,399
Granted Patent B2
US 11,123,399 · App. 16/466,165 · Granted Sep 21, 2021

Modulators of complement activity

Inventors: Alonso Ricardo (Cambridge, MA); Steven James DeMarco (Boxford, MA); Sylvia Tobe (Winchester, MA); Michelle Denise Hoarty (Billerica, MA); Robert Paul Hammer (Maynard, MA); Douglas A. Treco (Arlington, MA); Kathleen Seyb (Wakefield, MA); Vaishnavi Rajagopal (Andover, MA); Guo-Qing Tang (Acton, MA); Douangsone D. Vadysirisack (Boston, MA); Ramin Farzaneh-Far (Brookline, MA)
Assignee: RA PHARMACEUTICALS, INC.
A61K38/12A61K9/0019A61K39/3955A61P7/06
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Quick Facts
Patent No.
US 11,123,399
App. No.
16/466,165
Granted
Sep 21, 2021
Kind
B2
Abstract

The present disclosure relates to polypeptide modulators of complement activity, including cyclic polypeptide modulators. Included are methods of utilizing such modulators as therapeutics. Also provided are methods of measuring C5 and related complexes using C5 binding agents.

Claims (17)

1. A method of treating hemolysis in a subject, wherein the subject has not been previously treated with eculizumab, the method comprising:

administering a polypeptide to the subject at an initial loading dose, wherein the polypeptide comprises the amino acid sequence of SEQ ID NO: 1; and

administering the polypeptide to the subject at an initial treatment dose, wherein the initial treatment dose is administered two or more times at regular intervals after the initial loading dose.

2. The method of claim 1 , wherein lactate dehydrogenase (LDH) levels in the subject are monitored over the course of treatment.

3. The method of claim 1 , wherein the initial treatment dose is substituted with a modified treatment dose of the polypeptide after two weeks or more of administration with the initial treatment dose.

4. The method of claim 3 , wherein the modified treatment dose of the polypeptide includes an increased dose of the polypeptide.

5. The method of claim 4 , wherein the initial treatment dose is substituted with the modified treatment dose when subject LDH levels are equal to or less than 1.5 times the upper limit normal.

6. The method of claim 1 , wherein the initial loading dose comprises from about 0.1 mg/kg to about 0.6 mg/kg of the polypeptide.

7. The method of claim 1 , wherein the initial treatment dose comprises from about 0.1 mg/kg to about 0.3 mg/kg of the polypeptide.

8. The method of claim 7 , wherein the initial treatment dose is substituted with a modified treatment dose of from about 0.3 mg/kg to about 0.6 mg/kg of the polypeptide.

9. The method of claim 1 , wherein hemolysis in subject serum is reduced.

10. The method of claim 1 , wherein at least one administration of the polypeptide comprises self-administration.

11. The method of claim 10 , wherein the self-administration is monitored.

12. The method of claim 11 , wherein the self-administration is remotely monitored.

13. The method of claim 11 , wherein the self-administration is monitored using a smart device.

14. The method of claim 1 , wherein the regular intervals are from about every 12 hours to about every 168 hours.

15. The method of claim 1 , wherein the subject has PNH.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 20, 2025
From: RA PHARMACEUTICALS, INC.
To: UCB HOLDINGS, INC.
Reel/Frame 071466/0238 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 4, 2019
From: RICARDO, ALONSO; DEMARCO, STEVEN JAMES; TOBE, SYLVIA; HOARTY, MICHELLE DENISE; HAMMER, ROBERT PAUL; TRECO, DOUGLAS A.; SEYB, KATHLEEN; TANG, GUO-QING; RAJAGOPAL, VAISHNAVI; VADYSIRISACK, DOUANGSONE D.; FARZANEH-FAR, RAMIN
To: RA PHARMACEUTICALS, INC.
Reel/Frame 049366/0571 →
Continuity (5)
Provisional Application 62430959 · Dec 7, 2016
Provisional Application 62491702 · Apr 28, 2017
Provisional Application 62525284 · Jun 27, 2017
Provisional Application 62555711 · Sep 8, 2017
Related Publication 20200038477A1 · Feb 6, 2020
Cited By (1)
US 12,239,684