IP Library Granted Patent US 10,174,106
Granted Patent B2
US 10,174,106 · App. 15/315,572 · Granted Jan 8, 2019

Anti-neurotensin long fragment antibodies and uses thereof

Inventor: Patricia Forgez (Paris, FR)
Assignees: INSERM (Institut National de la Sante et de la Recherche Medicale); Universite Paris Descartes
C07K16/18A61K33/24A61K39/39558A61K45/06C07K16/26C07K16/30A61K2039/505A61K2039/507C07K2317/24C07K2317/34C07K2317/565C07K2317/73C07K2317/76
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Quick Facts
Patent No.
US 10,174,106
App. No.
15/315,572
Granted
Jan 8, 2019
Kind
B2
Abstract

The present invention relates to a neutralizing antibody which is capable of binding to neurotensin with high affinity. The antibody of the present invention neutralizes the activity of neurotensin, in particular the oncogenic activities of neurotensin. In particular, the present invention relates to a neutralizing antibody which binds to the human neurotensin long fragment, and having a heavy chain variable region which comprises a H-CDR1 region having at least 90% of identity with SEQ ID NO:2, a H-CDR2 region having at least 90% of identify with SEQ ID NO:3 and a H-CDR3 region having at least 90% of identity with SEQ ID NO:4; and a light chain variable region comprising a L-CDR1 region having at least 90% of identity with SEQ ID NO:6, a L-CDR2 having at least 90% of identity with SEQ ID NO:7 and a L-CDR3 region having at least 90% of identity with SEQ ID NO:8. The present invention also provides the use of such antibodies in the treatment of cancer.

Claims (7)

1. A neutralising antibody which binds to a human neurotensin, and has (i) a heavy chain variable region which comprises a H-CDR1 region as set forth in SEQ ID NO:2, a H-CDR2 region as set forth in SEQ ID NO:3 and a H-CDR3 region as set forth in SEQ ID NO:4; and (ii) a light chain variable region comprising a L-CDR1 region as set forth in SEQ ID NO:6, a L-CDR2 as set forth in SEQ ID NO:7 and a L-CDR3 region as set forth in SEQ ID NO:8.

2. The neutralising antibody of claim 1 wherein the heavy chain variable region has the amino acid sequence set forth as SEQ ID NO:1 and/or the light chain variable region has the amino acid sequence set forth as SEQ ID NO:5.

3. The neutralising antibody of claim 1 which is a chimeric antibody.

4. The neutralising antibody of claim 1 which is a humanized antibody.

5. The neutralising antibody of claim 1 which is selected from the group consisting of Fv, Fab, F(ab′)2, Fab′, dsFv, scFv, sc(Fv)2 and diabodies.

6. A pharmaceutical composition which comprises the neutralising antibody of claim 1 .

7. The neutralising antibody of claim 3 , wherein the chimeric antibody is a chimeric mouse/human antibody.

Assignments (3)
CHANGE OF NAME Recorded May 12, 2022
From: UNIVERSITE DE PARIS
To: UNIVERSITÉ PARIS CITÉ
Reel/Frame 059988/0388 →
MERGER Recorded May 12, 2022
From: UNIVERSITE PARIS DESCARTES
To: UNIVERSITE DE PARIS
Reel/Frame 060044/0856 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2017
From: FORGUEZ, PATRICIA
To: INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE); UNIVERSITÉ PARIS DESCARTES
Reel/Frame 041123/0306 →
Priority Claims (1)
EP 14305826 · Jun 2, 2014 · regional
Continuity (1)
Related Publication 20170218057A1 · Aug 3, 2017