- Trials with a EudraCT protocol (19)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
19 result(s) found for: GnRH analogues.
Displaying page 1 of 1.
EudraCT Number: 2017-003072-31 | Sponsor Protocol Number: 2378 | Start Date*: 2018-05-15 |
Sponsor Name:VU University Medical Center | ||
Full Title: The effects of sex hormone administration on marrow and visceral adiposity | ||
Medical condition: Healthy transgender persons (the effect of differences in sex hormones on the amount of bone marrow fat) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000212-89 | Sponsor Protocol Number: antagovo | Start Date*: 2008-03-04 |
Sponsor Name:Instituto Universitario IVI Valencia | ||
Full Title: Uso de antagonistas de la GnRH en la preparación endometrial de las receptoras de ovocitos. | ||
Medical condition: Comparar los resultados obtenidos con el empleo de antagonistas de la GnRH en la sincronización receptora de ovocitos–donante frente a los resultados obtenidos con el tradicional empleo de supresió... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003996-23 | Sponsor Protocol Number: SAKK08/16 | Start Date*: 2017-08-29 | |||||||||||
Sponsor Name:SAKK | |||||||||||||
Full Title: ODM-201 maintenance therapy in patients with metastatic castration resistant prostate cancer (mCRPC) previously treated with one novel hormonal agent first line and nonprogressive disease after sec... | |||||||||||||
Medical condition: Metastatic castration resistant prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Prematurely Ended) ES (Ongoing) FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001269-10 | Sponsor Protocol Number: Doc-Pred | Start Date*: 2016-07-14 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: A pharmacokinetic study of Docetaxel and Prednisone in men with metastatic castration-resistant or hormone-sensitive prostate cancer. | ||
Medical condition: Metastatic prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019810-26 | Sponsor Protocol Number: 1968 | Start Date*: 2011-09-09 | |||||||||||
Sponsor Name:King's College Hospital Foundtion NHS Trust | |||||||||||||
Full Title: A randomised controlled trial to investigate the effects of the use of pre-operative GnRH analogue and intra-operative mechanical tourniquet for myomectomy on surgical blood loss, future fertility ... | |||||||||||||
Medical condition: Uterine Fiboids | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003250-34 | Sponsor Protocol Number: IVI-ERA-2011 | Start Date*: 2011-12-13 | |||||||||||
Sponsor Name:IVI Madrid | |||||||||||||
Full Title: Endometrial receptivity with different support protocols for the luteal phase in ovarian stimulation cycles in which final oocyte maturation is carried out with GnRH analogues. Analysis by endometr... | |||||||||||||
Medical condition: Ovarian Hyperstimulation Syndrome (OHSS) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002965-39 | Sponsor Protocol Number: RHMCAN0890 | Start Date*: 2013-04-29 | |||||||||||
Sponsor Name:Swiss Group for Clinical Cancer Research (SAKK) | |||||||||||||
Full Title: Orteronel maintenance therapy in patients with metastatic castration resistant prostate cancer and non-progressive disease after first-line docetaxel therapy: A multicenter randomized double-blind ... | |||||||||||||
Medical condition: Castration Resistant Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000095-18 | Sponsor Protocol Number: 21656 | Start Date*: 2022-09-12 | ||||||||||||||||
Sponsor Name:Bayer Consumer Care AG | ||||||||||||||||||
Full Title: A double-blind, randomized, placebo-controlled multicenter study to investigate efficacy and safety of elinzanetant for the treatment of vasomotor symptoms caused by adjuvant endocrine therapy, ove... | ||||||||||||||||||
Medical condition: Vasomotor symptoms caused by adjuvant endocrine therapy in women with, or at high risk for developing hormone-receptor positive breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) HU (Trial now transitioned) ES (Trial now transitioned) FI (Trial now transitioned) BE (Trial now transitioned) FR (Trial now transitioned) PT (Trial now transitioned) IE (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003022-92 | Sponsor Protocol Number: 9785-CL-0403 | Start Date*: 2014-04-29 | |||||||||||
Sponsor Name:Astellas Pharma Global Development, Inc. | |||||||||||||
Full Title: A Multicenter, Single-Arm, Open-Label, Post-Marketing Safety Study to Evaluate the Risk of Seizure Among Subjects with Metastatic Castration-Resistant Prostate Cancer (mCRPC) Treated with Enzalutam... | |||||||||||||
Medical condition: Medical condition: metastatic castration-resistant prostate cancer (mCRPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) HU (Completed) GB (Completed) BE (Completed) FI (Completed) IT (Completed) CZ (Completed) GR (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001166-13 | Sponsor Protocol Number: COU-AA-001 | Start Date*: 2005-09-21 | |||||||||||
Sponsor Name:Cougar Biotechnology, Inc | |||||||||||||
Full Title: A Phase I/II Open Label Study of the 17α-hydroxylase/ C17,20 lyase inhibitor, Abiraterone acetate, in Patients with Prostate Cancer who have failed hormone therapy | |||||||||||||
Medical condition: Hormone refractory prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003865-32 | Sponsor Protocol Number: TOK-200-11 | Start Date*: 2014-02-12 | |||||||||||
Sponsor Name:Tokai Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Pharmacokinetic and Pharmacodynamic Translational Investigation of Galeterone in Patients with Metastatic Castration Resistant Prostate Cancer | |||||||||||||
Medical condition: Metastatic Castration Resistant Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005949-16 | Sponsor Protocol Number: 202000894 | Start Date*: 2021-10-25 | ||||||||||||||||||||||||||
Sponsor Name:University Medical Center Groningen | ||||||||||||||||||||||||||||
Full Title: A GnRH Agonist IN pre-menopausal women STudy to treat severe Polycystic Liver Disease | ||||||||||||||||||||||||||||
Medical condition: Severe polycystic liver disease in female patients | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: NL (Trial now transitioned) DE (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002832-15 | Sponsor Protocol Number: 49916 | Start Date*: 2014-12-17 | |||||||||||
Sponsor Name:VU university medical center | |||||||||||||
Full Title: Ulipristal versus Gonadotropin-releasing hormone agonists prior to laparoscopic myomectomy: a double blind randomized controlled trial | |||||||||||||
Medical condition: Uterine fibroids are very common during reproductive years in women. Minimally invasive treatments are emerging. Myomectomy is the gold standard which removes the fibroids entirely, preferably lapa... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001370-88 | Sponsor Protocol Number: IBCSG 35-07/ BIG 1-07 | Start Date*: 2007-11-06 | |||||||||||
Sponsor Name:International Breast Cancer Study Group (IBCSG) | |||||||||||||
Full Title: A phase III trial evaluating the role of continuous letrozole versus intermittent letrozole following 4 to 6 years of prior adjuvant endocrine therapy for postmenopausal women with hormone-receptor... | |||||||||||||
Medical condition: Postmenopausal women who are disease-free following 4-6 years of prior adjuvant endocrine therapy with selective estrogen receptor modulator(s) (SERM) and/or aromatase inhibitor(s) (AI) for endocri... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) HU (Completed) IT (Completed) DE (Completed) DK (Completed) GB (Completed) ES (Completed) SI (Completed) GR (Completed) AT (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001461-32 | Sponsor Protocol Number: OGX-011-12 | Start Date*: 2012-07-12 | ||||||||||||||||
Sponsor Name:OncoGenex Technologies Inc. | ||||||||||||||||||
Full Title: A Randomized Phase 3 Study Comparing Cabazitaxel/Prednisone in Combination with Custirsen (OGX-011) to Cabazitaxel/Prednisone for Second-Line Chemotherapy in Men with Metastatic Castrate Resistant ... | ||||||||||||||||||
Medical condition: Metastatic Castrate Resistant Prostate Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: GB (Completed) HU (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021011-16 | Sponsor Protocol Number: OGX-011-11 | Start Date*: 2010-09-27 | ||||||||||||||||
Sponsor Name:Teva Pharmaceutical Industries, Ltd | ||||||||||||||||||
Full Title: A Randomized Phase 3 Study Comparing Standard First-Line Docetaxel/Prednisone to Docetaxel/Prednisone in Combination with Custirsen (OGX-011) in Men with Metastatic Castrate Resistant Prostate Cancer | ||||||||||||||||||
Medical condition: metastatic castrate resistant prostate cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: HU (Completed) FR (Completed) DE (Completed) ES (Completed) BE (Completed) NL (Completed) GB (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001361-27 | Sponsor Protocol Number: ICR-CTSU/2015/10054 | Start Date*: 2016-09-21 | |||||||||||
Sponsor Name:The Institute of Cancer Research | |||||||||||||
Full Title: CTC-STOP: Utilising Circulating Tumour Cell (CTC) Counts to Optimize Systemic Therapy of Metastatic Prostate Cancer. | |||||||||||||
Medical condition: Advanced Castration Resistant Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004022-36 | Sponsor Protocol Number: CCR5316 | Start Date*: 2022-01-07 | |||||||||||
Sponsor Name:The Royal Marsden NHS Foundation Trust | |||||||||||||
Full Title: A randomised trial of early detection of molecular relapse with circulating tumour DNA tracking and treatment with palbociclib plus fulvestrant versus standard endocrine therapy in patients with ER... | |||||||||||||
Medical condition: Breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000209-10 | Sponsor Protocol Number: D8731C00002 | Start Date*: 2020-10-20 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II, Open-label Study to Assess the Efficacy, Safety, and Tolerability of AZD4635 in Combination with Durvalumab and in Combination with Cabazitaxel and Durvalumab in Patients Who Have Progr... | |||||||||||||
Medical condition: Progressive Metastatic Castrate-Resistant Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) FR (Completed) DK (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
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