Use of gnrh antagonists in mammals to synchronize follicular wave emergence
AssigneeUniversity of Saskatchewan
InventorsJaswant Singh, Gregg P. Adams, Carlos Eduardo Leonardi, Muhammad Anzar
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Abstract
The present disclosure relates to methods for reproductive management of mammalian animals using a GnRH antagonist such as Cetrorelix. Specifically, the GnRH antagonist can be used for synchronizing follicular wave emergence in a population of female mammals, and/or for fixed-time reproductive management protocols such as oocyte collection protocols, embryo collection protocols, artificial insemination protocols or embryo transfer protocols. Also described are devices and kits for reproductive management, comprising a GnRH antagonist and optionally one or more additional drugs useful for reproductive management.
Claims34
(canceled)
A non-therapeutic method of synchronizing ovulation in a population of female mammals, the method comprising:
- I)
- a) synchronizing follicular wave emergence (FWE) by administering an effective amount of a GnRH antagonist;
- and
- b) administering an effective amount of an ovulation inducing agent at a fixed time following the administration of the GnRH antagonist, to each mammal of the population of female mammals;
- or
- II)
- a) synchronizing follicular wave emergence (FWE) by administering an effective amount of a GnRH antagonist and an effective amount of progesterone or a progesterone analog;
- b) withdrawing administration of the progesterone or progesterone analog and administering an effective amount of prostaglandin (PGF) or a PGF analog at a fixed time following the administration of the GnRH antagonist;
- and
- c) administering an effective amount of an ovulation inducing agent at a fixed time following the withdrawal of progesterone or progesterone analog and/or administration of the PGF or PGF analog, to each mammal of the population of female mammals.
4-8. (canceled)
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17-28. (canceled)
A non-therapeutic method of inducing ovulation in a female mammal, the method comprising:
- I)
- a) initiating follicular wave emergence (FWE) by administering an effective amount of a GnRH antagonist to the female mammal;
- and
- b) administering an effective amount of an ovulation inducing agent at a fixed time following the administration of the GnRH antagonist;
- or
- II)
- a) initiating follicular wave emergence (FWE) by administering an effective amount of a GnRH antagonist to the female mammal;
- b) co-administering an effective amount of progesterone or a progesterone analog with the GnRH antagonist;
- c) withdrawing the progesterone or progesterone analog and administering an effective amount of prostaglandin (PGF) or a PGF analog at a fixed time following the administration of the GnRH antagonist;
- and
- d) administering an effective amount of an ovulation inducing agent at a fixed time following the withdrawal of the progesterone or progesterone analog and/or administration of the PGF or PGF analog.
31-32. (canceled)
A non-therapeutic fixed-time superstimulatory or superovulatory method, the method comprising:
- I)
- a) administering an effective amount of a GnRH antagonist to a female mammal;
- and b) administering an effective amount of FSH or an FSH agonist to the female mammal at a fixed time following the administration of the GnRH antagonist, provided that the FSH or FSH agonist is not co-administered with the GnRH antagonist, optionally further comprising administering an effective amount of an ovulation inducing agent at a fixed time following the administration of the FSH or FSH agonist;
- or
- II)
- a) administering an effective amount of a GnRH antagonist to a female mammal;
- b) co-administering an effective amount of progesterone or a progesterone analog with the GnRH antagonist;
- c) administering an effective amount of FSH or an FSH agonist to the female mammal at a fixed time following the administration of the GnRH antagonist, provided that the FSH or FSH agonist is not co-administered with the GnRH antagonist;
- and d) withdrawing the progesterone or progesterone analog and administering an effective amount of prostaglandin (PGF) or a PGF analog at a fixed time following the administration of the FSH or FSH agonist, optionally further comprising administering an effective amount of an ovulation inducing agent at a fixed time following the withdrawal of the progesterone or progesterone analog and/or administration of the PGF or PGF analog.
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36-37. (canceled)
41-42. (canceled)
44-45. (canceled)
47-52. (canceled)
Dependencies are inferred from the claim text.