IP Library Granted Patent US 10,233,245
Granted Patent B2
US 10,233,245 · App. 15/596,468 · Granted Mar 19, 2019

Methods of treating inflammatory and autoimmune diseases with natalizumab

Inventor: Ivan Lieberburg (Berkeley, CA)
Assignee: BIOGEN MA INC.
C07K16/2839A61K38/03A61K38/215A61K39/3955A61K39/39541A61K45/06A61K49/0004C07K16/2842G01N33/6893G01N33/6896A61K2039/505A61K2039/54A61K2039/545C07K2317/24G01N2333/025G01N2800/065G01N2800/285G01N2800/7095Y02A50/467
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Quick Facts
Patent No.
US 10,233,245
App. No.
15/596,468
Granted
Mar 19, 2019
Kind
B2
Abstract

Natalizumab is a safe and efficacious treatment for inflammatory and autoimmune diseases, such as multiple sclerosis, Crohn's Disease, and rheumatoid arthritis. Rare occurrences of progressive multifocal leucoencephalopathy during treatment suggest the possibility that it may be related to natalizumab treatment. Monitoring for JCV and informing caregivers and patients about the manifestations of progressive multifocal leucoencephalopathy can improve the safety of natalizumab therapy.

Claims (28)

1. A method of using natalizumab to treat a patient with an inflammatory or autoimmune disease, the method comprising:

(a) testing the patient for the presence of anti-JC virus (JCV) antibodies by a method consisting of determining a presence or absence of anti-JCV antibodies in serum or plasma of a blood sample of a patient;

(b) identifying the patient as having serum or plasma that is negative for anti-JCV antibodies; and

(c) initiating natalizumab treatment of the patient having serum or plasma that is negative for anti-JCV antibodies,

wherein the testing of (a) improves the safety of the natalizumab treatment.

2. The method of claim 1 , further comprising:

(d) monitoring the patient for indicators of progressive multifocal leukoencephalopathy (PML) after initiating natalizumab treatment of the patient,

wherein the testing of (a) and monitoring of (d) improve the safety of the natalizumab treatment.

3. The method of claim 2 , further comprising discontinuing the administration of natalizumab in the presence of the indicators of PML.

4. The method of claim 2 , wherein the indicators of PML comprise new or worsening neurological symptoms.

5. The method of claim 4 , wherein the neurological symptoms comprise one or more of central blindness, mental confusion, personality change, and dyskinesia.

6. The method of claim 2 , wherein the monitoring the patient for indicators of PML after initiating natalizumab treatment of the patient comprises detecting the presence of JCV in the patient's cerebrospinal fluid.

7. The method of claim 2 , wherein the monitoring the patient for indicators of PML after initiating natalizumab treatment of the patient comprises serially removing samples of the patient's blood, measuring the amount of IgG antibodies to JCV in the samples, and comparing the amount of the antibodies in the samples.

8. The method of claim 7 , wherein the monitoring the patient for indicators of PML further comprises:

(i) detecting seroconversion or an increasing titer of JCV by the comparing the amount of the antibodies in the samples;

(ii) removing a sample of the patient's cerebrospinal fluid after detecting the seroconversion or increasing titer of JCV; and

(iii) testing the cerebrospinal fluid for the presence of JCV.

9. The method of claim 2 , wherein the indicators of PML comprise new or worsening radiological symptoms.

10. The method of claim 9 , wherein the radiologic symptoms comprise lesions detected by a Gd-enhanced magnetic resonance imaging scan.

11. The method of claim 1 , wherein the inflammatory or autoimmune disease is multiple sclerosis.

12. The method of claim 11 , wherein the multiple sclerosis is selected from relapsing remitting, secondary progressive, primary progressive, and chronic progressive multiple sclerosis.

13. The method of claim 12 , wherein the multiple sclerosis (MS) is relapsing remitting MS.

14. The method of claim 12 , wherein the multiple sclerosis (MS) is secondary progressive MS.

15. The method of claim 12 , wherein the multiple sclerosis (MS) is primary progressive MS.

16. The method of claim 12 , wherein the multiple sclerosis is chronic progressive multiple sclerosis.

17. The method of claim 1 , wherein the disease is inflammatory bowel disease.

18. The method of claim 17 , wherein the inflammatory bowel disease is Crohn's disease.

19. The method of claim 1 , wherein the disease is rheumatoid arthritis.

Assignments (4)
CHANGE OF NAME Recorded Aug 9, 2018
From: BIOGEN IDEC MA INC.
To: BIOGEN MA INC.
Reel/Frame 046754/0694 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 8, 2018
From: BIOGEN IDEC INTERNATIONAL HOLDING LTD.
To: BIOGEN IDEC MA INC.
Reel/Frame 047227/0374 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 8, 2018
From: LIEBERBURG, IVAN
To: ELAN PHARMACEUTICALS, INC.
Reel/Frame 046590/0365 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 8, 2018
From: ELAN PHARMACEUTICALS, INC.
To: BIOGEN IDEC INTERNATIONAL HOLDING LTD.
Reel/Frame 046749/0683 →
Continuity (5)
Continuation 15285381 · Oct 4, 2016
Continuation 12757305 · Apr 9, 2010
Division 11711628 · Feb 28, 2007
Provisional Application 60776931 · Feb 28, 2006
Related Publication 20170247457A1 · Aug 31, 2017
Cited By (4)
US 12,221,416 US 12,345,703 US 12,392,784 US 12,607,638