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Original Article

Bioequivalence of recombinant human FSH and recombinant human LH in a fixed 2 : 1 combination: two phase I, randomised, crossover studies

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Pages 1199-1208 | Accepted 27 Feb 2008, Published online: 17 Mar 2008

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Read on this site (5)

Ahmed Gibreel & Siladitya Bhattacharya. (2010) Recombinant follitropin alfa/lutropin alfa in fertility treatment. Biologics: Targets and Therapy 4, pages 5-17.
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Ernesto Bosch. (2009) Recombinant human FSH and recombinant human LH in a 2:1 ratio combination: a new tool for ovulation induction. Expert Review of Obstetrics & Gynecology 4:5, pages 491-498.
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Articles from other publishers (7)

Wilhelmina Bagchus, Özkan Yalkinoglu & Peter Wolna. (2018) Open-Label, Randomized, Two-Way, Crossover Study Assessing the Bioequivalence of the Liquid Formulation versus the Freeze-Dried Formulation of Recombinant Human FSH and Recombinant Human LH in a Fixed 2:1 Combination (Pergoveris®) in Pituitary-Suppressed Healthy Women. Frontiers in Endocrinology 8.
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Carlo Alviggi, Alessandro Conforti, Pasquale De Rosa, Raffaele Riccardi, Alessandra Abbamondi & Giuseppe De Placido. 2018. Encyclopedia of Reproduction. Encyclopedia of Reproduction 9 15 .
Sandro C. Esteves & Carlo Alviggi. 2015. Principles and Practice of Controlled Ovarian Stimulation in ART. Principles and Practice of Controlled Ovarian Stimulation in ART 171 196 .
Rogério de Barros Ferreira Leão & Sandro C. Esteves. 2015. Unexplained Infertility. Unexplained Infertility 293 322 .
Rogério de Barros F. Leão & Sandro C. Esteves. (2014) Gonadotropin therapy in assisted reproduction: an evolutionary perspective from biologics to biotech. Clinics 69:4, pages 279-293.
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Klaus Bühler, Olaf GJ Naether & Wilma Bilger. (2014) A large, multicentre, observational, post-marketing surveillance study of the 2:1 formulation of follitropin alfa and lutropin alfa in routine clinical practice for assisted reproductive technology. Reproductive Biology and Endocrinology 12:1, pages 6.
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Sanjeeva Dissanayake. (2010) Assessing the bioequivalence of analogues of endogenous substances (‘endogenous drugs’): considerations to optimize study design. British Journal of Clinical Pharmacology 69:3, pages 238-244.
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