IP Library Granted Patent US 11,820,813
Granted Patent B2
US 11,820,813 · App. 16/994,770 · Granted Nov 21, 2023

Anti-neurotensin long fragment antibodies and uses thereof

Inventor: Patricia Forgez (Paris, FR)
Assignees: INSERM (INSITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE); UNIVERSITE PARIS DESCARTES
C07K16/18A61K33/243A61K39/39558A61K45/06C07K16/26C07K16/30A61K2039/505A61K2039/507C07K2317/24C07K2317/34C07K2317/565C07K2317/73C07K2317/76C12N5/10C12N15/00C12N15/63
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,820,813
App. No.
16/994,770
Granted
Nov 21, 2023
Kind
B2
Abstract

The present invention relates to a neutralising antibody which is capable of binding to neurotensin with high affinity. The antibody of the present invention neutralises the activity of neurotensin, in particular the oncogenic activities of neurotensin. In particular, the present invention relates to a neutralising 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 (3)

1. A nucleic acid comprising a sequence which encodes a neutralizing antibody which binds to human neurotensin, said neutralizing antibody comprising 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 set forth in SEQ ID NO:4; and 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. A vector which comprises the nucleic acid sequence of claim 1 .

3. A host cell which has been transfected, infected or transformed to include the nucleic acid sequence of claim 1 .

Assignments (4)
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 →
CORRECTIVE ASSIGNMENT TO CORRECT THE SUPPORTING DOCUMENTATION PREVIOUSLY RECORDED AT REEL: 053508 FRAME: 0512. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Aug 26, 2020
From: FORGEZ, PATRICIA
To: INSERM (INSITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE); UNIVERSITE PARIS DESCARTES
Reel/Frame 053603/0713 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2020
From: FORGEZ, PATRICIA
To: INSERM (INSITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE); UNIVERSITE PARIS DESCARTES
Reel/Frame 053508/0512 →