IP Library Patent Application 13978723
Patent Application
App. No. 13/978,723

NOVEL USES

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Quick Facts
Patent No.
US None
App. No.
13/978,723
Abstract

A method of treating, arresting or preventing a disease responsive to treatment with an anti-CD20 antibody in a patient suffering therefrom, comprising administering to the patient at least one sub-depleting dose of antiCD20 antibody is disclosed.

Claims (31)

1 . A method of treating, arresting or preventing multiple sclerosis comprising in a human patient comprising administering an anti-CD20 antibody at:

(a) initial 3 mg dose followed by 30 mg at week one, and 30 mg at week 12; or

(b) intial 3 mg dose followed by 60 mg at week one, and 60 mg at week 12; or

(c) initial 3 mg dose followed by 60 mg at every four weeks for 24 weeks; or

(d) initial 3 mg dose followed by 30 mg at every four weeks for 24 weeks; or

(e) initial 3 mg dose, followed by 10 mg at every twelve weeks for 24 weeks; or

(f) 30 mg at week one, and 30 mg at week 12; or

(g) 60 mg at week one, and 60 mg at week 12; or

(h) 60 mg at every four weeks for 24 weeks; or

(i) 30 mg at every four weeks for 24 weeks; or

(j) 3 mg at week one, and 3 mg at week 12; or

(k) 10 mg at week one, and at every twelve weeks for 24 weeks.

2 . The method of claim 1 in which administration is subcutaneous.

3 . The method of claim 1 in which multiple sclerosis is relapse-remitting multiple sclerosis.

4 . The method of claim 1 in which multiple sclerosis is primary progressive multiple sclerosis.

5 . The method of claim 1 in which multiple sclerosis is secondary progressive multiple sclerosis.

6 . A method of treating, arresting or preventing patient spino-optical sclerosis or neuromyelitis optica in a human patient comprising administering an anti-CD20 antibody at

(a) initial 3 mg dose followed by 30 mg at week one, and 30 mg at week 12; or

(b) intial 3 mg dose followed by 60 mg at week one, and 60 mg at week 12; or

(c) initial 3 mg dose followed by 60 mg at every four weeks for 24 weeks; or

(d) initial 3 mg dose followed by 30 mg at every four weeks for 24 weeks; or

(e) initial 3 mg dose, followed by 10 mg at every twelve weeks for 24 weeks; or

(f) 30 mg at week one, and 30 mg at week 12; or

(g) 60 mg at week one, and 60 mg at week 12; or

(h) 60 mg at every four weeks for 24 weeks; or

(i) 30 mg at every four weeks for 24 weeks; or

(j) 3 mg at week one, and 3 mg at week 12; or

(k) 10 mg at week one, and at every twelve weeks for 24 weeks.

7 . The method of claim 1 in which the anti-CD20 is ofatumuamb.

8 . The method of claim 1 in which the anti-CD20 is rituximab.

9 . The method of claim 1 in which the anti-CD20 is ocrelizumab.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 3, 2015
From: NOVARTIS PHARMA AG
To: NOVARTIS AG
Reel/Frame 035812/0424 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 2, 2015
From: GLAXOSMITHKLINE INTELLECTUAL PROPERTY MANAGEMENT LIMITED
To: NOVARTIS PHARMA AG
Reel/Frame 035805/0811 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2015
From: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY MANAGEMENT LIMITED
Reel/Frame 034680/0917 →