Literature DB >> 10718102

Ganirelix.

P S Gillies1, D Faulds, J A Balfour, C M Perry.   

Abstract

Ganirelix is a synthetic third generation gonadotropin-releasing hormone (GnRH) antagonist that is administered via the subcutaneous route. The drug competitively blocks GnRH receptors in the anterior pituitary gland, preventing endogenous GnRH from inducing luteinising hormone (LH) and follicle stimulating hormone release. Ganirelix effectively inhibited LH surges during controlled ovarian stimulation in a large, multicentre clinical trial in women undergoing in vitro fertilisation. A vital pregnancy rate per embryo transfer of 40.3% was achieved at weeks 5 to 6 after treatment with the 0.25 mg/day dosage. Subcutaneous ganirelix has been generally well tolerated in clinical trials. The most common adverse events were local injection site events, asthenia, nausea, malaise, headache and fatigue.

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Year:  2000        PMID: 10718102     DOI: 10.2165/00003495-200059010-00007

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  12 in total

1.  Pharmacokinetic and pharmacodynamic characteristics of ganirelix (Antagon/Orgalutran). Part II. Dose-proportionality and gonadotropin suppression after multiple doses of ganirelix in healthy female volunteers.

Authors:  J J Oberyé; B M Mannaerts; J A Huisman; C J Timmer
Journal:  Fertil Steril       Date:  1999-12       Impact factor: 7.329

2.  Pharmacokinetic and pharmacodynamic characteristics of ganirelix (Antagon/Orgalutran). Part I. Absolute bioavailability of 0.25 mg of ganirelix after a single subcutaneous injection in healthy female volunteers.

Authors:  J J Oberyé; B M Mannaerts; H J Kleijn; C J Timmer
Journal:  Fertil Steril       Date:  1999-12       Impact factor: 7.329

3.  Control of the preovulatory Luteinizing Hormone surge by Gonadotropin-Releasing Hormone antagonists: prospects for clinical application.

Authors:  H M Fraser; P Bouchard
Journal:  Trends Endocrinol Metab       Date:  1994-03       Impact factor: 12.015

4.  First established pregnancy after controlled ovarian hyperstimulation with recombinant follicle stimulating hormone and the gonadotrophin-releasing hormone antagonist ganirelix (Org 37462).

Authors:  J Itskovitz-Eldor; S Kol; B Mannaerts; H Coelingh Bennink
Journal:  Hum Reprod       Date:  1998-02       Impact factor: 6.918

5.  High dose gonadotrophin-releasing hormone antagonist (ganirelix) may prevent ovarian hyperstimulation syndrome caused by ovarian stimulation for in-vitro fertilization.

Authors:  D de Jong; N S Macklon; B M Mannaerts; H J Coelingh Bennink; B C Fauser
Journal:  Hum Reprod       Date:  1998-03       Impact factor: 6.918

Review 6.  Gonadotropin-releasing hormone and its analogues: from laboratory to bedside.

Authors:  M R Henzl
Journal:  Clin Obstet Gynecol       Date:  1993-09       Impact factor: 2.190

7.  Endocrine effects and pharmacokinetic characteristics of a potent new gonadotropin-releasing hormone antagonist (Ganirelix) with minimal histamine-releasing properties: studies in postmenopausal women.

Authors:  J Rabinovici; P Rothman; S E Monroe; C Nerenberg; R B Jaffe
Journal:  J Clin Endocrinol Metab       Date:  1992-11       Impact factor: 5.958

8.  A double-blind, randomized, dose-finding study to assess the efficacy of the gonadotrophin-releasing hormone antagonist ganirelix (Org 37462) to prevent premature luteinizing hormone surges in women undergoing ovarian stimulation with recombinant follicle stimulating hormone (Puregon). The ganirelix dose-finding study group.

Authors: 
Journal:  Hum Reprod       Date:  1998-11       Impact factor: 6.918

Review 9.  Pharmacokinetics of anti-endocrine agents.

Authors:  P E Lønning; E A Lien
Journal:  Cancer Surv       Date:  1993

Review 10.  Recombinant follicle-stimulating hormone: new biotechnology for infertility.

Authors:  R R Prevost
Journal:  Pharmacotherapy       Date:  1998 Sep-Oct       Impact factor: 4.705

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  3 in total

1.  Noninvasive analytical estimation of endogenous GnRH drive: analysis using graded competitive GnRH-receptor antagonism and a calibrating pulse of exogenous GnRH.

Authors:  Daniel M Keenan; Iain J Clarke; Johannes D Veldhuis
Journal:  Endocrinology       Date:  2011-10-25       Impact factor: 4.736

2.  Low Drug Loading Hampers the Clinical Translation of Peptide Drugs-Containing Metered-Dose Inhalers.

Authors:  Zhengwei Huang; Lei Shu; Ying Huang; Chuanbin Wu; Xin Pan
Journal:  Pharmaceuticals (Basel)       Date:  2022-03-23

Review 3.  Optimal usage of the GnRH antagonists: a review of the literature.

Authors:  Alan B Copperman; Claudio Benadiva
Journal:  Reprod Biol Endocrinol       Date:  2013-03-15       Impact factor: 5.211

  3 in total

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