Jean‐Pierre Gotteland

No ORCID on file · 15 papers in corpus · active 2008-2022

Study types

  • article 15

Condition tags

  • endometriosis 11
  • mesh:D004715 5
  • mesh:D017699 2
  • mesh:D004412 1
  • chronic_pelvic_pain 1
  • dysmenorrhea 1
  • dyspareunia 1
article 2022
·doi:10.1093/humrep/deac105.103

Abstract Study question Is once-daily linzagolix treatment for women with moderate to severe endometriosis-associated pain (EAP) safe for use for up to 6 months of treatment? Summary answer Both doses of linzagolix were well-tolerated with …

article 2021
British journal of clinical pharmacology ·doi:10.1111/bcp.15171

AIMS: To identify linzagolix doses, an oral GnRH receptor antagonist, that effectively lower oestradiol (E2) to relieve endometriosis-related pelvic pain without compromising bone health. METHODS: Integrated statistical, pharmacokinetic-pha…

article 2020
Reproductive sciences (Thousand Oaks, Calif.) ·doi:10.1007/s43032-020-00172-z
article 2020
·doi:10.1097/01.aog.0000663180.46470.c9

INTRODUCTION: Linzagolix is a new, investigational, non-peptide, GnRH receptor antagonist being developed to treat endometriosis-associated pain (EAP). The EDELWEISS trial was a Phase 2b, double-blind, randomized, placebo-controlled, multic…

article 2020
·doi:10.1097/01.aog.0000663200.75027.38

INTRODUCTION: Linzagolix is a new investigational, non-peptide, oral GnRH receptor antagonist being developed to treat endometriosis-associated pain (EAP). The EDELWEISS trial was a Phase 2b, double-blind, randomized, placebo-controlled, mu…

article 2020
Fertility and sterility ·doi:10.1016/j.fertnstert.2020.02.114
article 2019
·doi:10.1016/j.fertnstert.2019.07.935
article 2019
·doi:10.1097/01.aog.0000558837.48634.b6

INTRODUCTION: Linzagolix is a new, non-peptide, GnRH receptor antagonist being developed to treat endometriosis-associated pain (EAP). The EDELWEISS trial is a Phase 2b, double-blind, randomized, placebo-controlled, multicenter, dose-rangin…

article 2017
·doi:10.1210/jc.2017-01875

Context: OBE2109 is a potent, oral gonadotropin-releasing hormone receptor antagonist being developed for the treatment of sex-hormone-dependent diseases in women. Objective: We assessed the pharmacodynamics and safety of OBE2109 alone and …

article 2015
Reproductive sciences (Thousand Oaks, Calif.) ·doi:10.1177/1933719115600553
article 2015
Fertility and sterility ·doi:10.1016/j.fertnstert.2015.11.022
article 2014
Reproductive sciences (Thousand Oaks, Calif.) ·doi:10.1177/1933719114522526
article 2011
Human Reproduction ·doi:10.1093/humrep/der079

BACKGROUND: Steroid sulfatase (STS) is involved in estrogen biosynthesis and expressed in eutopic and ectopic endometrium of disease-free and endometriosis patients. The present study was designed to investigate its role in endometriosis de…

article 2011
·doi:10.1097/ogx.0b013e31823d8bed

Endometriosis is an estrogen-dependent disorder. Treatment with hormonal therapy suppresses estrogen and leads to regression of lesions. However, hormonal therapy is associated with significant morbidity, adverse effects, and recurrence of …

article 2008
·doi:10.1093/biolreprod/78.s1.113b

Endometriosis is one of the most common causes of chronic pelvic pain, which affects over 70 million adult and adolescent women worldwide. The pathophysiology of endometriosis involves endocrine, inflammatory and angiogenic components and t…