IP Library Granted Patent US 10,179,816
Granted Patent B2
US 10,179,816 · App. 15/333,519 · Granted Jan 15, 2019

Pharmaceutical compositions comprising an antibody which binds the human anti-Müllerian hormone receptor type II

Inventors: Christine Gaucher (Equedin, FR); Isabelle Navarro-Teulon (Saint Gely du Fesc, FR)
Assignees: LABOTATOIRE FRANCAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES; ICM INSTITUT REGIONAL DU CANCER DE MONTPELLIER; I.N.S.E.R.M. (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE); UNIVERSITE DE MONTPELLIER
C07K16/2869A61K9/0019A61K31/282A61K31/337A61K33/24A61K39/3955A61K39/39533A61K39/39558A61K45/06C07K16/28C07K16/3069A61K2039/505C07K2317/24C07K2317/92
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Quick Facts
Patent No.
US 10,179,816
App. No.
15/333,519
Granted
Jan 15, 2019
Kind
B2
Abstract

The invention relates to novel pharmaceutical compositions including, as active ingredient, an antibody binding the human anti-Müllerian hormone type II receptor (AMHR-II) and an anticancer agent, as well as the therapeutic applications of these compositions.

Claims (36)

1. Pharmaceutical composition comprising, as active ingredient, in combination with a pharmaceutically acceptable vehicle,

an anticancer agent chosen among olaparib, rucaparib and bevacizumab, and

a mutated humanized 12G4 monoclonal antibody binding the human anti-Müllerian hormone type II receptor (AMHR-II) comprising:

a) a light chain comprising:

a variable region the amino acid sequence of which is represented by SEQ ID NO: 7 or SEQ ID NO: 8,

a constant region the amino acid sequence of which is represented by SEQ ID NO: 3

b) a heavy chain comprising:

a variable region the amino acid sequence of which is represented by SEQ ID NO: 9 or SEQ ID NO: 10,

a constant region the amino acid sequence of which is represented by SEQ ID NO: 6.

2. Composition according to claim 1 , in which said antibody possesses affinity for AMHR-II characterized by a K D less than 10 −7 M.

3. Pharmaceutical composition according to claim 1 , in which the antibody is produced by the 3C23K.

4. Pharmaceutical composition according to claim 1 , in which said antibody is a recombinant antibody produced by animal transgenesis.

5. Pharmaceutical composition according to claim 1 , comprising the mutated 12G4 monoclonal antibody produced by the 3C23K clone, and olaparib.

6. Pharmaceutical composition according to claim 1 , comprising the mutated 12G4 monoclonal antibody produced by the 3C23K clone, and rucaparib.

7. Pharmaceutical composition according to claim 1 , in a formulation intended for administration by the intravenous or intraperitoneal route.

8. Pharmaceutical composition according to claim 1 , in which the therapeutically effective quantity of antibody administered to a patient is in a range from about 0.07 mg to about 35000 mg.

9. Pharmaceutical composition according to claim 1 , in which the therapeutically effective quantity of anticancer agent administered to a patient is in a range from about 10 mg to about 700 mg.

10. Pharmaceutical composition according to claim 1 , in which the dose of antibody administered to a patient is about 70 mg and the dose of anticancer agent administered to the patient is about 110 mg.

11. Pharmaceutical composition according to claim 1 , comprising the mutated 12G4 monoclonal antibody produced by the 3C23K clone, and bevacizumab.

12. Method for treating a pathology associated with the human anti-Müllerian hormone type II receptor (AMHR-II) comprising the administration of a therapeutically effective quantity of the composition comprising:

an anticancer agent chosen among olaparib, rucaparib and bevacizumab, and

a mutated humanized 12G4 monoclonal antibody binding the human anti-Müllerian hormone type II receptor (AMHR-II) comprising or constituted by:

a) a light chain comprising or constituted by:

a variable region the amino acid sequence of which is represented by SEQ ID NO: 7 or SEQ ID NO: 8,

a constant region the amino acid sequence of which is represented by SEQ ID NO: 3

b) a heavy chain comprising or constituted by:

a variable region the amino acid sequence of which is represented by SEQ ID NO: 9 or SEQ ID NO: 10,

a constant region the amino acid sequence of which is represented by SEQ ID NO: 6.

13. The method of claim 12 wherein the quantity of the antibody administered to a patient is in a range from about 0.07 mg to about 35000 mg.

14. The method of claim 12 wherein the quantity of antibody administered is from 0.1 mg/kg to 100 mg/kg.

15. The method of claim 12 wherein the quantity of anticancer agent administered to a patient is in a range from about 20 mg to about 350 mg.

16. The method of claim 12 wherein the quantity of anticancer agent administered to a patient is about 110 mg.

17. Method for treating a pathology, according to claim 12 , in which the pathology associated with the human anti-Müllerian hormone type II receptor (AMHR-II) is cancer.

18. Method for treating a pathology according to claim 12 , in which the cancer is an ovarian cancer.

19. Method for treating a pathology according to claim 12 , in which the cancer is an endometrial cancer.

20. Method for treating a pathology according to claim 12 , in which the cancer is a mixed Müllerian malignant tumor of the uterus.

Assignments (4)
CHANGE OF ADDRESS Recorded Jun 9, 2022
From: LABORATOIRE FRANÇAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
To: LABORATOIRE FRANÇAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
Reel/Frame 060316/0783 →
CHANGE OF NAME Recorded May 18, 2018
From: CENTRE REGIONAL DE LUTTE CONTRE LE CANCER
To: ICM INSTITUT REGIONAL DU CANCER DE MONTPELLIER
Reel/Frame 046185/0188 →
MERGER Recorded May 18, 2018
From: UNIVERSITE MONTPELLIER I
To: UNIVERSITE DE MONTPELLIER
Reel/Frame 046836/0321 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 25, 2016
From: GAUCHER, CHRISTINE; NAVARRO-TULON, ISABELLE
To: LABORATOIRE FRANCAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES; CENTRE REGIONAL DE LUTTE CONTRE LE CANCER; I.N.S.E.R.M. (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE); UNIVERSITE MONTPELLIER 1
Reel/Frame 040118/0505 →
Priority Claims (1)
FR 11 62424 · Dec 23, 2011 · national
Continuity (2)
Division 14367969
Related Publication 20170101478A1 · Apr 13, 2017