- Trials with a EudraCT protocol (554)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
554 result(s) found for: Sperm count.
Displaying page 1 of 28.
EudraCT Number: 2009-017940-15 | Sponsor Protocol Number: P081227 | Start Date*: 2010-04-20 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Devenir de la spermatogénèse chez les hommes drépanocytaires traités médicalement (HYDREP). | |||||||||||||
Medical condition: Drépanocytose | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000402-38 | Sponsor Protocol Number: GS-US-418-4279 | Start Date*: 2018-01-19 | ||||||||||||||||
Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Phase 2 Study to Evaluate the Testicular Safety of Filgotinib in Adult Males with Moderately to Severely Active Inflammatory Bowel Disease | ||||||||||||||||||
Medical condition: To evaluate the testicular safety of filgotinib in adult males with moderately to severely Active Inflammatory Bowel Disease | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) AT (Completed) PT (Prematurely Ended) NL (Prematurely Ended) SE (Prematurely Ended) BE (Prematurely Ended) ES (Prematurely Ended) RO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000655-24 | Sponsor Protocol Number: CBG-study2 | Start Date*: 2015-04-28 | |||||||||||
Sponsor Name:rigshospitalet | |||||||||||||
Full Title: Denosumab and male infertility: a prospective intervention study | |||||||||||||
Medical condition: Male infertility especially low sperm count | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004254-37 | Sponsor Protocol Number: 000400 | Start Date*: 2022-06-27 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled trial to assess the efficacy and safety of FE 999049 for treatment of men with idiopathic infertility | |||||||||||||
Medical condition: Idiopathic male infertility (including oligoasthenozoospermia) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: SE (Trial now transitioned) DE (Trial now transitioned) ES (Trial now transitioned) DK (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003933-14 | Sponsor Protocol Number: GLPG0634-CL-227 | Start Date*: 2019-05-27 | ||||||||||||||||||||||||||
Sponsor Name:Galapagos NV | ||||||||||||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Phase 2 Study to Evaluate the Effect of Filgotinib on Semen Parameters in Adult Males with active Rheumatoid Arthritis, Psoriatic Arthritis, Ankylosin... | ||||||||||||||||||||||||||||
Medical condition: Rheumatoid Arthritis, Psoriatic Arthritis, Ankylosing Spondylitis and Non-radiographic Axial Spondyloarthritis | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: LV (Completed) EE (Completed) BG (Completed) BE (Completed) CZ (Completed) ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000722-19 | Sponsor Protocol Number: M12-919 | Start Date*: 2016-10-24 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Multicenter, Single-Arm Study of the Effects of Atrasentan on Spermatogenesis and Testicular Function | |||||||||||||
Medical condition: Diabetic Nephropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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: 2007-005315-26 | Sponsor Protocol Number: A25165 | Start Date*: 2008-07-01 | |||||||||||
Sponsor Name:CONRAD, Eastern Virgina Medical School | |||||||||||||
Full Title: Sperm Suppression and Contraceptive Protection provived by Norethisterone Enantate (NET-EN) combined with Testosterone Undecanoate (TU) in healthy men. | |||||||||||||
Medical condition: The proposed study is designed to evaluate whether the combination of a progestin, norethisterone enantate (NET-EN), and an androgen, testosterone undecanoate (TU), represents a safe and effective ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) IT (Temporarily Halted) GB (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004032-21 | Sponsor Protocol Number: ARGX-113-2004 | Start Date*: 2021-05-07 | |||||||||||
Sponsor Name:argenx BV | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blinded, Placebo-Controlled Trial to Evaluate the Efficacy and the Safety of Efgartigimod (ARGX-113) PH20 Subcutaneous in Adult Patients With Primary Immu... | |||||||||||||
Medical condition: Primary immune thrombocytopenia (ITP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) PT (Completed) DE (Completed) BG (Completed) NO (Completed) DK (Completed) GR (Completed) IT (Completed) FR (Completed) RO (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002521-19 | Sponsor Protocol Number: FSH_IMEN | Start Date*: 2015-10-19 | |||||||||||
Sponsor Name:Instituto de Investigación Sanitaria La Fe | |||||||||||||
Full Title: "Pilot study on the effect of FSH treatment in epigenetic characteristics of sperm in infertile patients with severe oligozoospermia" | |||||||||||||
Medical condition: Male infertility | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003006-27 | Sponsor Protocol Number: GEXGP24201 | Start Date*: 2012-11-27 | |||||||||||
Sponsor Name:Glycotope GmbH | |||||||||||||
Full Title: A Phase II, Multicentre, Multinational, Randomised, Assessor-Blind Trial to Investigate the Efficacy and Safety of Various Dosages of FSH-GEX™ in Comparison With 150 IU Gonal-f® in Women Undergoing... | |||||||||||||
Medical condition: women undergoing intracytoplasmatic sperm injection (ICSI) as part of assisted reproduction | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004176-35 | Sponsor Protocol Number: RIST4721-201 | Start Date*: 2019-04-10 | |||||||||||
Sponsor Name:Aristea Therapeutics Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 2a Study to Evaluate the Efficacy and Safety of RIST4721 in Subjects with Palmoplantar Pustulosis | |||||||||||||
Medical condition: Palmoplantar Pustulosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000884-26 | Sponsor Protocol Number: TP0003 | Start Date*: 2020-03-20 | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: A Phase 3 Multicenter, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Rozanolixizumab in Adult Study Participants With Persistent or Chroni... | |||||||||||||
Medical condition: Primary Immune Thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) BG (Prematurely Ended) HU (Completed) BE (Completed) CZ (Completed) AT (Prematurely Ended) ES (Prematurely Ended) NL (Completed) GB (GB - no longer in EU/EEA) FR (Prematurely Ended) GR (Completed) IT (Prematurely Ended) HR (Completed) RO (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003451-11 | Sponsor Protocol Number: TP0006 | Start Date*: 2020-04-30 | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: A Phase 3 Multicenter, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Rozanolixizumab in Adult Study Participants With Persistent or Chroni... | |||||||||||||
Medical condition: Primary Immune Thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) PL (Prematurely Ended) FR (Prematurely Ended) DE (Prematurely Ended) BE (Completed) CZ (Prematurely Ended) AT (Prematurely Ended) ES (Prematurely Ended) NL (Completed) GB (GB - no longer in EU/EEA) IT (Prematurely Ended) DK (Prematurely Ended) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003038-26 | Sponsor Protocol Number: ARGX-113-1603 | Start Date*: 2017-02-08 | |||||||||||
Sponsor Name:Argenx BVBA | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Phase II Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of ARGX-113 in Patients with Primary Immune Thrombocytopenia, followed by an Op... | |||||||||||||
Medical condition: Primary Immune Thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) CZ (Completed) BE (Completed) DE (Completed) AT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002100-41 | Sponsor Protocol Number: ARGX-113-1801 | Start Date*: 2019-11-01 | |||||||||||
Sponsor Name:argenx BVBA | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blinded, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of Efgartigimod (ARGX-113) 10 mg/kg Intravenous in Adult Patients With Primary Immun... | |||||||||||||
Medical condition: Primary immune thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FR (Completed) HU (Completed) CZ (Completed) ES (Completed) PL (Completed) BE (Completed) DE (Completed) AT (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001981-13 | Sponsor Protocol Number: INCB54707204 | Start Date*: 2021-03-02 | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study of the Efficacy and Safety of INCB054707 in Participants With Hidradenitis Suppurativa | |||||||||||||
Medical condition: Hidradenitis Suppurativa | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004683-22 | Sponsor Protocol Number: RGCH005 | Start Date*: 2020-10-16 | |||||||||||
Sponsor Name:Ostfold Hospital Trust | |||||||||||||
Full Title: Daratumumab as a treatment for adult immune thrombocytopenia | |||||||||||||
Medical condition: Immune thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) FR (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002101-21 | Sponsor Protocol Number: ARGX-113-1803 | Start Date*: 2020-05-25 | |||||||||||
Sponsor Name:argenx BV | |||||||||||||
Full Title: A Phase 3, Multicenter, Open-label, Long-term Trial to Evaluate the Safety and Efficacy of Efgartigimod (ARGX-113) 10 mg/kg Intravenous in Adult Patients With Primary Immune Thrombocytopenia | |||||||||||||
Medical condition: Primary immune thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) ES (Completed) HU (Trial now transitioned) FR (Completed) BE (Completed) CZ (Trial now transitioned) BG (Completed) DE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) IT (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004677-27 | Sponsor Protocol Number: ABX464-301 | Start Date*: 2019-09-16 | |||||||||||
Sponsor Name:Abivax | |||||||||||||
Full Title: Phase IIa randomized, double blind, placebo controlled, parallel group, multiple dose study on ABX464 in combination with methotrexate (MTX), in patients with moderate to severe active Rheumatoid A... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
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