- Trials with a EudraCT protocol (10)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10 result(s) found for: Hypergonadotropic hypogonadism.
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EudraCT Number: 2007-005640-25 | Sponsor Protocol Number: Tostran2v1 | Start Date*: 2008-05-08 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Greater Glasgow & Clyde Health Board | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Effect of Tostran 2% Gel on Growth, Development & Bone Turnover in Hypogonadal Adolescent Boys | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Delayed puberty or hypogonadism in boys requiring pubertal induction. | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001012-11 | Sponsor Protocol Number: NAT-2017-01 | Start Date*: 2017-08-01 | ||||||||||||||||
Sponsor Name:Acerus Biopharma Inc. | ||||||||||||||||||
Full Title: A multicenter, open label, variable dose, two arm pilot paediatric phase 1 PK study to evaluate testosterone nasal gel (4.5% w/w) in hypogonadal boys | ||||||||||||||||||
Medical condition: Primary and secondary hypogonadism | ||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004532-10 | Sponsor Protocol Number: POI-1 | Start Date*: 2018-05-23 | |||||||||||
Sponsor Name:Karolinska University Hospital | |||||||||||||
Full Title: Effects of immunomodulatory therapy on gonadal function in women with autoimmune premature ovarian insufficiency | |||||||||||||
Medical condition: Autoimmune premature ovarian insufficiency | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Ongoing) NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002304-33 | Sponsor Protocol Number: no sponsor | Start Date*: 2006-09-12 | |||||||||||
Sponsor Name:Rijnstate Hospital | |||||||||||||
Full Title: Letrozole Treatment to Normalize Serum Testosterone in Men with Hypogonadotropic Hypogonadism due to Pituitary Damage. | |||||||||||||
Medical condition: Hypogonadotropic hypogonadism in men with pituitary damage other than irradiation | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002155-25 | Sponsor Protocol Number: TAK-448-2001 | Start Date*: 2014-11-17 | |||||||||||
Sponsor Name:Takeda Development Centre Europe Ltd | |||||||||||||
Full Title: An Open-Label, Phase 2a Study to Evaluate the Pharmacodynamics of Different Dosing Regimens of TAK-448, a Kisspeptin Agonist, in Male Overweight/Obese Subjects With Hypogonadotropic Hypogonadism | |||||||||||||
Medical condition: Hypogonadotropic Hypogonadism | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004677-12 | Sponsor Protocol Number: RHYTHM | Start Date*: 2021-02-09 | |||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI MODENA E REGGIO EMILIA - DIPARTIMENTO DI SCIENZE BIOMEDICHE, METABOLICHE E NEUROSCIENZE | |||||||||||||
Full Title: Pharmacodynamics and safety of human recombinant luteinising hormone in hypogonadotropic hypogonadal men. | |||||||||||||
Medical condition: Aquired hypogonadotropic hypogonadism | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001258-25 | Sponsor Protocol Number: MK8962-031-00 | Start Date*: 2012-11-29 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A phase III, multi-center, open label, uncontrolled trial to investigate the efficacy and safety of MK-8962 (corifollitropin alfa) in combination with human Chorionic Gonadotropin (hCG) in inducing... | |||||||||||||
Medical condition: Hypogonadotropic hypogonadism (HH) in males may result from either absent or inadequate gonadotropin-releasing hormone (GnRH) secretion by the hypothalamus or failure of pituitary gonadotropin secr... | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Completed) GB (Completed) PL (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004729-42 | Sponsor Protocol Number: 22102014 | Start Date*: 2015-04-13 | |||||||||||
Sponsor Name:Odense University Hospital, department M [...] | |||||||||||||
Full Title: The effect of testosterone replacement in patients with hypogonadotroph hypogonadism due to opioid treatment for non-malignant disease A double-blinded, randomized and placebo-controlled trial | |||||||||||||
Medical condition: Male Hypogonadism | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005760-42 | Sponsor Protocol Number: MBGS205 | Start Date*: 2016-05-25 | |||||||||||
Sponsor Name:Mereo BioPharma 2 Limited | |||||||||||||
Full Title: A Phase IIb multicentre, double-blind, dose-ranging, randomised, placebo-controlled study evaluating safety and efficacy of BGS649 in male obese subjects with hypogonadotropic hypogonadism | |||||||||||||
Medical condition: Hypogonadotropic hypogonadism (HH) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001878-18 | Sponsor Protocol Number: MK8962-043 | Start Date*: 2017-07-19 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III, Multi-Center, Open Label, Single-Group Trial to Investigate the Efficacy and Safety of MK-8962 (corifollitropin alfa) in Combination with human Chorionic Gonadotropin (hCG) for Initiat... | |||||||||||||
Medical condition: Treatment of adolescent males 14 to <18 years old with HH | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) DK (Prematurely Ended) Outside EU/EEA | |||||||||||||
Trial results: View results |
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