IP Library Granted Patent US 7,393,834
Granted Patent B2
US 7,393,834 · App. 10/661,780 · Granted Jul 1, 2008

LHRH-antagonists in the treatment of fertility disorders

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Quick Facts
Patent No.
US 7,393,834
App. No.
10/661,780
Granted
Jul 1, 2008
Kind
B2
Abstract

A method of treating infertility disorders by 1) administering an LH-RH antagonist, preferably Cetrorelix, in amounts to selectively suppress endogenous LH but not FSH secretion and 2) inducing follicle growth by administration of exogenous gonadotropin. The selective suppression OF LH allows FSH secretion to be at natural levelS thereby not affecting individual estrogen development. The LH-RH antagonist can be given as a single or dual subcutaneous dose in the range of 1 mg to 10 mg, preferably 2 mg-6 mg. In multiple dosing-posology, LH-RH antagonist can be administered subcutaneously in an amount in the range of 0.1 to 0.5 mg of LH-RH antagonist/day. LH-RH antagonist is applied starting cycle day 1 to 10, preferably on day 4 to 8, and ovulation can be induced between day 9 and 20 of the menstruation cycle by administering rec. LH, native LH-RH, LH-RH agonist or by HCG. In addition rec. LH, native LH-RH or LH-RH agonist can be given to avoid hyperstimulation syndrome and native LH-RH or a LH-RH agonist can be administered to avoid luteal phase stimulation by neutralizing the negative effects of HCG.

Claims (28)

1. A method of treating infertility disorders comprising

administering an LHRH-antagonist selected from the group consisting of ganirelix, antarelix, antide, azaline B, ramorelix, A-76154, Nal-Glu, 88-88 and cetrorelix, and inducing follicle growth by administration of hMG or recombinant FSH (Controlled Ovarian Stimulation) in combination with clomiphene, wherein the administration of said LHRH-antagonist is sufficient to suppress endogenous LH while maintaining FSH secretion at a natural level and estrogen development is not affected until ovulation induction.

2. The method according to claim 1 , wherein Controlled Ovarian Stimulation is started on day 2 after spontaneous menstrual bleeding by administering 100 mg clomiphene per day for 3 to 7 days and 0.2 to 1.0 mg cetrorelix is administered with hMG starting on stimulation day 5.

3. The method according to claim 1 , wherein Controlled Ovarian Stimulation is started on day 2 after spontaneous menstrual bleeding by administering 100 mg clomiphene per day for 3 to 7 days and 0.2 to 1.0 mg cetrorelix is administered with recombinant FSH starting on stimulation day 6.

4. The method according to claim 3 , wherein cetrorelix is administered subcutaneously in an amount between 0.1 and 5 mg per day during a multiple dosing regimen.

5. The method according to claim 1 , wherein the LHRH antagonist is administered as a single or dual subcutaneous dose in an amount between 1 and 10 mg.

6. The method according to claim 5 , wherein the LHRH antagonist is administered as a single or dual subcutaneous dose in an amount between 2 and 6 mg.

7. The method according to claim 1 , wherein the LHRH antagonist is administered as an initial single dose in the range of 1 mg to 10 mg, followed by a multiple daily dose in an amount between 0.2 and 1.0 mg.

8. The method according to claim 7 , wherein the single dose is between 2 and 6 mg.

9. The method according to claim 1 , wherein ovulation is induced by administration of FSH or LH.

10. The method according to claim 1 , wherein ovulation is induced by administration of LHRH or LHRH agonist.

11. The method according to claim 1 , wherein ovulation is induced by human chorionic gonadotropin (HCG).

12. The method according to claim 1 , wherein LHRH or an LHRH antagonist is administered so that luteal phase supplementation is avoided and negative effects of HCG are prevented during the luteal phase.

13. The method according to claim 1 , wherein FSH, LH, LHRH, or LHRH agonist is administered so that ovarian hyperstimulation syndrome is avoided.

14. A method of treating infertility disorders comprising administering an amount of cetrorelix as an LHRH antagonist which is sufficient to suppress endogenous LH while maintaining FSH secretion at a natural level and not affecting estrogen development and further administering clomiphene to induce follicle growth, wherein after cessation of cetrorelix administration, subsequent follicle development is facilitated with remaining endogenous LH and FSH.

15. The method of claim 14 , wherein cetrorelix is administered beginning on cycle day 6 to 10 and ovulation is induced between day 7 and day 11 of the menstrual cycle.

16. The method of claim 14 , wherein cetrorelix is administered either in a single or dual dose of 1 to 10 mg or in a multiple dosage of 0.1 to 0.5 mg starting at cycle day 1 to 10 and ovulation is induced between day 9 and day 20 of the menstrual cycle.

17. The method according to claim 16 , wherein cetrorelix is administered starting on cycle day 4 to 9.

18. A method of Controlled Ovarian Stimulation (COS) comprising

administering an LHRH antagonist selected from the group consisting of ganirelix, antarelix, antide, azaline B, ramorelix, A-76154, Nal-Glu, 88-88 and cetrorelix, and inducing follicle growth by administration of hMG or FSH in combination with clomiphene, wherein the administration of said LHRH antagonist is sufficient to suppress endogenous LH while maintaining FSH secretion at a natural level and estrogen development is not affected until ovulation induction.

19. A method of Controlled Ovarian Stimulation comprising administering an amount of cetrorelix as an LHRH antagonist which is sufficient to suppress endogenous LH while maintaining FSH secretion at a natural level and not affecting estrogen development and further administering clomiphene to induce follicle growth, wherein after cessation of cetrorelix administration, subsequent follicle development and ovulation is facilitated by endogenous LH and FSH.

20. A method of treating fertility disorders treatable by controlled ovarian stimulation and assisted reproduction techniques, comprising

administering an LHRH antagonist selected from the group consisting of ganirelix, antarelix, antide, azaline B, ramorelix, A-76154, Nal-Glu, 88-88 and cetrorelix, and inducing follicle growth by administration of hMG or FSH (Controlled Ovarian Stimulation) in combination with clomiphene,

wherein the administration of said LHRH antagonist is sufficient to suppress endogenous LH while maintaining FSH secretion at a natural level and estrogen development is not affected until ovulation induction; and

performing assisted reproduction techniques following induction of ovulation.

21. A method of treating infertility disorders treatable by controlled ovarian stimulation and assisted reproduction techniques, comprising

administering an amount of cetrorelix as an LHRH antagonist which is sufficient to suppress endogenous LH while maintaining FSH secretion at a natural level and not affecting estrogen development and further administering clomiphene to induce follicle growth, wherein after cessation of cetrorelix administration, subsequent follicle development and ovulation is facilitated with remaining endogenous LH and FSH, and

performing assisted reproduction techniques following ovulation.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2012
From: AETERNA ZENTARIS GMBH
To: ZENTARIS IVF GMBH
Reel/Frame 027886/0381 →
CHANGE OF NAME Recorded Feb 2, 2012
From: ZENTARIS GMBH
To: AETERNA ZENTARIS GMBH
Reel/Frame 027646/0117 →
SECURITY AGREEMENT Recorded Nov 22, 2011
From: ZENTARIS IVF GMBH
To: CETRO INVESTORS, L.P.
Reel/Frame 027278/0053 →
SECURITY AGREEMENT Recorded Nov 22, 2011
From: COWEN HEALTHCARE ROYALTY PARTNERS, L.P. (SUCCESSOR OF CETRO INVESTORS, L.P.); VANDERBILT ROYALTY HOLDINGS L.P.; VANDERBILT ROYALTY SUB L.P.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 027278/0184 →
CHANGE OF NAME Recorded Mar 7, 2006
From: ZENTARIS AG
To: ZENTARIS GMBH
Reel/Frame 017289/0495 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 2, 2006
From: ASTA MEDICA GMBH
To: ZENTARIS AG
Reel/Frame 017242/0779 →