Drugs / Cetrorelix
last change 11 days ago re-read 9 days ago

Cetrorelix

Other / unclassified

Developed for
infertility disorder · ovarian hyperstimulation syndrome · polycystic ovary syndrome · benign prostatic hyperplasia · endometriosis · female infertility · ovarian cyst · primary ovarian failure
+4 more · rheumatoid arthritis · ectopic pregnancy · leiomyoma · ovarian disorder
Investigated by
AEterna Zentaris · Damascus University · Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) · Instituto Valenciano de Infertilidad, IVI VALENCIA · University of Colorado, Denver · Al-Azhar University
+40 more · Aljazeera Hospital · Assaf-Harofeh Medical Center · Assistance Publique - Hôpitaux de Paris · Bart CJM Fauser · Beni-Suef University · Betanien Hospital · Bezmialem Vakif University · Bioroma · Cairo University · ClinAmygate · EMD Serono · Eugonia · Ibn Sina Hospital · Institute for Human Reproduction (IHR) · Merck KGaA, Darmstadt, Germany · Merck Serono International SA · Merck Serono S.A.S, France · MerckSerono Pharmaceuticals · National Heart, Lung, and Blood Institute (NHLBI) · Nippon Kayaku Co., Ltd. · Northwest Women's and Children's Hospital, Xi'an, Shaanxi · Norwegian Foundation for Health and Rehabilitation · Oxford Fertility Limited, United Kingdom · Pınar Özcan Cenksoy · Rigshospitalet, Denmark · Seoul National University Bundang Hospital · Seoul National University Hospital · ShangHai Ji Ai Genetics & IVF Institute · Shionogi · Solvay Pharmaceuticals · Tanta University · The University of Texas at Arlington · Trust Fertility Clinic · URC-CIC Paris Descartes Necker Cochin · University Hospital, Basel, Switzerland · University of Oslo · University of Oxford · University of Texas Southwestern Medical Center · Università degli Studi 'G. d'Annunzio' Chieti e Pescara · Virginia Center for Reproductive Medicine

Regulatory milestones approvals, filings & regulatory actions · 2 recorded

MilestoneJurisdictionBrandIndicationDateSentence it was read from
Approved US (FDA) CETROTIDE — 2000-08-11 fda.gov ↗
Approved EU (EMA) Cetrotide — 1999-04-12 europa.eu ↗

Trials 40

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 01 trial
Phase 0 NCT02042196 Dec 2013 → May 2016 — University of Colorado, Denver Completed No outcome recorded
Phase 23 trials · 2 met primary
Phase 2 NCT02461875 May 2013 → Nov 2015 ovarian hyperstimulation syndrome Aljazeera Hospital Unknown Met primary
Phase 2 NCT00667758 May 2008 → Jun 2011 rheumatoid arthritis Betanien Hospital Completed Met primary
Phase 2 NCT00244452 Nov 2005 → Sep 2006 endometriosis Solvay Pharmaceuticals Completed No outcome recorded
Phase 37 trials · 3 missed
Phase 3 NCT04414761 Jun 2020 → Oct 2022 — ShangHai Ji Ai Genetics & IVF Institute Completed Missed primary
Phase 3 NCT01268761 Apr 2012 → Jul 2013 ovarian hyperstimulation syndrome Instituto Valenciano de Infertilidad, IVI VALENCIA Completed No outcome recorded
Phase 3 NCT01402336 Jun 2011 → Dec 2016 infertility disorder, polycystic ovary syndrome Seoul National University Hospital Completed No outcome recorded
Phase 3 NCT01185704 Nov 2008 → Oct 2011 polycystic ovary syndrome Merck KGaA, Darmstadt, Germany Completed No outcome recorded
Phase 3 NCT00663858 Mar 2008 → Sep 2009 benign prostatic hyperplasia AEterna Zentaris Completed Missed primary
Phase 3 NCT00670306 Mar 2008 → Aug 2009 benign prostatic hyperplasia AEterna Zentaris Completed No outcome recorded
Phase 3 NCT00449150 Mar 2007 → Jun 2009 benign prostatic hyperplasia AEterna Zentaris Terminated Missed primary
Phase 419 trials · 1 met primary · 2 missed
Phase 4 NCT07350317 Jan → Dec 2026 expected — Trust Fertility Clinic Not yet recruiting No outcome recorded
Phase 4 NCT04993924 May 2021 → Mar 2022 ovarian cyst Assaf-Harofeh Medical Center Unknown No outcome recorded
Phase 4 NCT04754243 Mar 2021 → Dec 2024 infertility disorder Tanta University Unknown No outcome recorded
Phase 4 NCT04727684 Aug 2020 → Feb 2022 infertility disorder, polycystic ovary syndrome Damascus University Completed No outcome recorded
Phase 4 NCT04724486 Aug 2020 → Mar 2022 infertility disorder Damascus University Completed No outcome recorded
Phase 4 NCT04727671 Dec 2019 → Aug 2021 infertility disorder, polycystic ovary syndrome Damascus University Completed No outcome recorded
Phase 4 NCT04724343 Dec 2019 → Jan 2022 infertility disorder Damascus University Completed No outcome recorded
Phase 4 NCT03996434 Jul → Nov 2019 ovarian hyperstimulation syndrome ClinAmygate Completed Met primary
Phase 4 NCT03763786 Dec 2018 → Jan 2021 infertility disorder University of Oxford Unknown No outcome recorded
Phase 4 NCT04671966 Sep 2018 → Dec 2024 heart disorder The University of Texas at Arlington Unknown No outcome recorded
Phase not applicable10 trials
— NCT06023602 Feb 2024 → Dec 2025 overdue infertility disorder Northwest Women's and Children's Hospital, Xi'an, Shaanxi Recruiting No outcome recorded
— NCT05767086 Mar 2023 → Sep 2024 infertility disorder Bezmialem Vakif University Completed No outcome recorded
— NCT04052607 Sep 2019 → Apr 2020 infertility disorder Ibn Sina Hospital Terminated No outcome recorded
— NCT02392520 May 2015 → Mar 2016 ovarian hyperstimulation syndrome Eugonia Unknown No outcome recorded
— NCT01565265 Apr → Dec 2012 female infertility University Hospital, Basel, Switzerland Completed No outcome recorded
— NCT01457703 Jun 2010 → Jul 2013 obesity disorder University of Colorado, Denver Completed No outcome recorded
— NCT00867659 Mar 2009 → Oct 2011 ovarian hyperstimulation syndrome Virginia Center for Reproductive Medicine Completed No outcome recorded
— NCT00571870 Nov 2007 → Aug 2009 infertility disorder Seoul National University Bundang Hospital Completed No outcome recorded
— NCT00460642 Jan 2007 → Oct 2009 infertility disorder Institute for Human Reproduction (IHR) Completed No outcome recorded
— NCT00628121 Apr 2006 → Feb 2007 — Nippon Kayaku Co., Ltd. Completed No outcome recorded
Comparator or background therapy61 trials
Phase 0 NCT02640976 Comparator Jun 2013 → Jun 2015 female infertility Cairo University Completed No outcome recorded
Phase 1/2 NCT06608186 Comparator Oct 2024 → Jan 2025 polycystic ovary syndrome Ahmed Saad Completed No outcome recorded
Phase 1/2 NCT04071574 Comparator Feb 2018 → Aug 2019 ectopic pregnancy, endometriosis, female infertility, hydrosalpinx +6 Lebanese University Completed No outcome recorded
Phase 1/2 NCT01109888 Comparator — ovarian hyperstimulation syndrome Wolfson Medical Center Withdrawn No outcome recorded Stop: Enrollment
Phase 2 NCT06212102 Comparator May 2024 → Mar 2027 expected infertility disorder Bedaya Hospital Recruiting No outcome recorded

Evidence & citations 11 cited values

Every value below carries the sentence it was read from. 102 sources stand behind the page.

FieldValueCited text
Known as cetrorelix “Our specific aim is to compare the rates of ovarian preservation in reproductive age women receiving chemotherapeutic agents known to affect ovarian function who receive...” NCT00507780 ↗
61

“antagonist group :Multiple dose gonadotrophin-releasing hormone antagonist regimen will be used for ovarian stimulation 0.25 microgram per day cetrorelix will be administered...” NCT03139474 ↗

“GnRH antagonist (cetrorelix acetate)(Cetrotide®) 0.25 mg S.C once daily is started when the leading follicle is 14 mm in mean diameter and is continued until and including the...” NCT04268927 ↗

“Cetrorelix (Cetrotide©, 250 mcg/mL, Pierre Fabre Medicament Production, Idron, France) 1x1 SC will be started on day 7 of menstrual cycle and will be continued until the trigger day.” NCT06396390 ↗

“Premenopausal women will be treated with the gonadotropin-releasing hormone (GnRH) antagonist Cetrorelix for 6 days in order to suppress ovarian sex hormones.” NCT04671966 ↗

“GnRH antagonist (Cetrorelix or Ganirelix 0.25mg) once subcutaneously daily from day 6 of ovarian stimulation till the day of the ovulation trigger” NCT04414761 ↗

“Patients were randomized to androgen priming (n = 53): anastrozole 1 mg cycle day (c.d.) 2, 3 and 4, hCG 1250 IU and cetrorelix 3 mg on c.d. 2” PMID 18487212 ↗ May 2008

“GnRH antagonist (Cetrorelix 0.25mg) once subcutaneously daily from day 6 of ovarian stimulation till the day of the ovulation trigger” NCT05447208 ↗

“GnRH antagonist (Cetrorelix 0.25mg) once subcutaneously daily from day 6 of ovarian stimulation till the day of the ovulation trigger” NCT05326087 ↗

“Flexible GnRH antagonist protocol (Cetrorelix acetate) (0.2 mg) was used to prevent premature LH surge during the FPS and LPS.” NCT06212102 ↗

“Cetrorelix is a widely used GnRH antagonist, and Prolutex® is a subcutaneous formulation of bioidentical progesterone” NCT07350317 ↗

Show 51 more sources

Known as AEZS-102 “Cetrorelix Pamoate (AEZS-102) in Patients With Symptomatic BPH: a Double-blind Placebo-controlled Efficacy Study” NCT00663858 ↗
Known as cetrorelex acetate “This study will examine whether the drug cetrorelex acetate (Cetrotide\[Registed Trademark\]) can protect ovarian function in women undergoing chemotherapy.” NCT00507780 ↗
Known as cetrorelix acetate “GnRH antagonist (cetrorelix acetate)(Cetrotide®) 0.25 mg S.C once daily is started when the leading follicle is 14 mm in mean diameter and is continued until and including the...” NCT04268927 ↗
18

“Cetrorelix acetate, a GnRH (Gonadotropin releasing hormone) antagonist administered subcutaneously, is the current standard for luteinizing hormone suppression.” NCT07350317 ↗

“In a recent case series by Sauer et al, cetrorelix acetate, a GnRH antagonist, was given in doses of 3mg at four day intervals to four patients ages 21-30.” NCT00507780 ↗

“Gn RH agonist (triptorelin) is discontinued and GnRH antagonist (Cetrorelix acetate)0.25 mg S.C is administered daily till the day of HCG administration.” NCT02461875 ↗

“Ganirelix acetate or cetrorelix acetate Agonist is used to suppress endogenous pituitary LH for the premature LH surges.” NCT01669291 ↗

“Cetrorelix Type: Drug Arm: B Description: Cetrorelix acetate 0.25 mg administered by daily subcutaneous injection” NCT07732348 ↗

“GnRH antagonist (Cetrorelix acetate) (Cetrotide; Serono International S.A., Geneva, Switzerland)” NCT03373149 ↗

“cetrorelix acetate 0.25 started on stimulation day 6 till the trigger day to prevent LH surge.” NCT04052607 ↗

“Cetrorelix acetate 0,25 mg/d starting five days after ovarian stimulation” NCT02821819 ↗

“Cetrorelix acetate 0.25 mg” NCT03996434 ↗

NCT01185704 ↗

Show 8 more sources

Known as Cetrorelix Pamoate “Cetrorelix Pamoate (AEZS-102) in Patients With Symptomatic BPH: a Double-blind Placebo-controlled Efficacy Study” NCT00663858 ↗
Known as Cetrotide “GnRH antagonist (cetrorelix acetate)(Cetrotide®) 0.25 mg S.C once daily is started when the leading follicle is 14 mm in mean diameter and is continued until and including the...” NCT04268927 ↗
36

“The Gonadotropins releasing hormone antagonist GnRH ant (Cetrotide, Serono, Geneva, Switzerland) was given when the leading follicle was from 12 to 14 mm, at a daily dose of 0.25 mg SC.” NCT02335736 ↗

“Cetrorelix (Cetrotide©, 250 mcg/mL, Pierre Fabre Medicament Production, Idron, France) 1x1 SC will be started on day 7 of menstrual cycle and will be continued until the trigger day.” NCT06396390 ↗

“GnRH antagonist Cetrorelix (CETROTIDE 0.25Mg/d, Merck Serono, Germany) 0.25 mg/day subcutaneously from day 6 of induction until trigger day.” NCT05951400 ↗

“When the leading follicle reached 12 mm, GnRH antagonist was started using Cetrotide 0.25 subcutaneously daily till the day of triggering.” NCT04008966 ↗

“Ovulation by blocking the GnRH antagonist (gonadotropin-releasing hormone : CETROTIDE) introduced according to the usual criteria,” NCT02890082 ↗

“GnRH antagonist (Cetrorelix acetate) (Cetrotide; Serono International S.A., Geneva, Switzerland)” NCT03373149 ↗

“daily s.c. administration of Cetrotide 0.25 mg will be initiated at 6th day of stimulation” NCT05112692 ↗

“GnRH antagonist (Cetrotide®, Merck-Serono, Switzerland) 0.25 mg subcutaneously daily” NCT04157725 ↗

“The GnRH antagonist, cetrorelix acetate (Cetrotide; Serono) 0.25 mg was added daily” NCT00571870 ↗

“0.25 mg of cetrotide (Merck-Serono ,Germany) will be injected subcutaneously daily” NCT05847660 ↗

Show 26 more sources

Known as cetrotide acetate ClinicalTrials.gov intervention name — accepted as the source's own label NCT00867659 ↗
Known as Cetrotide\[Registed Trademark\] “This study will examine whether the drug cetrorelex acetate (Cetrotide\[Registed Trademark\]) can protect ovarian function in women undergoing chemotherapy.” NCT00507780 ↗
Action Inhibit “GnRH antagonist” NCT00286364 ↗
Modality Other / unclassified “GnRH antagonist” NCT01468441 ↗
Route Subcutaneous “Cetrotide® will be administered subcutaneously” NCT00298025 ↗