IP Library Granted Patent US 10,570,198
Granted Patent B2
US 10,570,198 · App. 15/047,541 · Granted Feb 25, 2020

Stable and soluble antibodies

Inventors: Leonardo Jose Borras (Schlieren, CH); David Urech (Jona, CH)
Assignee: NOVARTIS AG
C07K16/241C07K2317/24C07K2317/31C07K2317/56C07K2317/622C07K2317/76C07K2317/94
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Quick Facts
Patent No.
US 10,570,198
App. No.
15/047,541
Granted
Feb 25, 2020
Kind
B2
Abstract

The invention provides antibodies that are modified to reduce aggregration propensity, and methods of producing such antibodies. The present invention also provides particularly stable and soluble scFv antibodies and Fab fragments specific for TNF, which comprise specific light chain and heavy chain sequences that are optimized for stability, solubility, in vitro and in vivo binding of TNF, and low immunogenicity. The nucleic acids, vectors and host cells for expression of the recombinant antibodies of the invention, methods for isolating them and the use of said antibodies in medicine are also disclosed.

Claims (5)

1. A method of blocking the function of TNFα in a subject, the method comprising administering to the subject a pharmaceutical composition comprising an antibody having the sequence of SEQ ID NO: 10, wherein the subject has dry eye, and wherein the pharmaceutical composition is administered topically to an eye of the subject.

2. The method of claim 1 , wherein the pharmaceutical composition is administered in a single or divided dose comprising 0.1 to 100 mg of the antibody.

3. A method of reducing TNFα-mediated inflammation in a subject in need thereof, the method comprising administering to a subject a therapeutically effective amount of an antibody that comprises a variable light chain that has an Arginine at Aho position 50 and the sequence of SEQ ID NO: 2, and a variable heavy chain comprising the sequence of SEQ ID NO: 5, wherein the subject has dry eye, and wherein the pharmaceutical composition is administered topically to an eye of the subject.

4. The method of claim 3 , wherein the therapeutically effective amount of the antibody is in a range of about 0.1 to 100 mg/kg of patient body weight.

5. The method of claim 3 , wherein the antibody comprises the sequence of SEQ ID NO: 10.

Assignments (3)
CONFIRMATORY LICENSE Recorded Nov 18, 2020
From: NOVARTIS AG
To: OCULIS SA
Reel/Frame 054458/0814 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 8, 2019
From: BORRAS, LEONARDO JOSE; URECH, DAVID
To: ESBATECH, AN ALCON BIOMEDICAL RESEARCH UNIT LLC
Reel/Frame 050959/0558 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 8, 2019
From: ESBATECH, A NOVARTIS COMPANY LLC
To: NOVARTIS AG
Reel/Frame 050969/0094 →
Cited By (1)
US 12,637,521