- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
14 result(s) found for: Cyproterone Acetate.
Displaying page 1 of 1.
EudraCT Number: 2005-002409-21 | Sponsor Protocol Number: 358 | Start Date*: 2005-11-09 |
Sponsor Name:Population Council - Center for Biomedical Research | ||
Full Title: A dose-finding randomized clinical trial to evaluate the differential impact of four progestins for their use as male contraceptives in healthy men. | ||
Medical condition: This clinical trial tests several products for their future usefulness for male contraception. | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000502-19 | Sponsor Protocol Number: PSY-NIL-0002 | Start Date*: 2016-06-21 |
Sponsor Name:Medical University of Vienna, Department of Psychiatry and Psychotherapy | ||
Full Title: Effects of sex steroid hormones on serotonin synthesis and degradation measured with PET | ||
Medical condition: Gender Dysphoria (Female-to-male transsexuals and male-to-female transsexuals) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004545-15 | Sponsor Protocol Number: MLAM 2007/01 | Start Date*: 2008-06-10 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: The Split Dose Study: Split dose Rhenium-188-HEDP regimen in hormone refractory prostate cancer patients with bone metastases; a phase I toxicity study and phase II efficacy study. | ||
Medical condition: Hormone refractory prostate cancer with painful bone metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-001030-33 | Sponsor Protocol Number: MRCPR09 | Start Date*: 2005-11-23 |
Sponsor Name:University College London | ||
Full Title: PATCH Prostate Adenocarcinoma: TransCutaneous Hormones A randomised-controlled trial of transcutaneous oestrogen patches versus LHRH agonists in prostate cancer. | ||
Medical condition: Newly diagnosed or relapsing patients with locally advanced or metastatic prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004564-32 | Sponsor Protocol Number: NG 05 / 09 | Start Date*: 2007-03-06 | |||||||||||
Sponsor Name:University Medical center Utrecht | |||||||||||||
Full Title: The Prostate CARE Study: Capecitabine (Xeloda®) combined with Rhenium-188-HEDP in hormone refractory prostate cancer patients with bone metastases; a Capecitabine phase I dose escalation study and... | |||||||||||||
Medical condition: Hormone refractory prostate cancer with painful bone metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001440-99 | Sponsor Protocol Number: ANB019-208 | Start Date*: 2021-08-25 | |||||||||||
Sponsor Name:AnaptysBio Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Subjects with Hidradenitis Suppurativa | |||||||||||||
Medical condition: Hidradenitis Suppurativa | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018109-29 | Sponsor Protocol Number: MINALO3004 | Start Date*: 2010-07-05 | |||||||||||
Sponsor Name:Johnson & Johnson Healthcare Products Division of McNEIL-PPC, Inc. | |||||||||||||
Full Title: A PHASE 3 MULTI-CENTER PARALLEL DESIGN CLINICAL TRIAL TO COMPARE THE EFFICACY AND SAFETY OF 5% MINOXIDIL FOAM VS. 2% MINOXIDIL SOLUTION IN FEMALES FOR THE TREATMENT OF FEMALE PATTERN HAIR LOSS (AND... | |||||||||||||
Medical condition: FEMALE PATTERN HAIR LOSS (ANDROGENETIC ALOPECIA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019881-96 | Sponsor Protocol Number: MINALO3005 | Start Date*: 2010-11-19 | |||||||||||
Sponsor Name:Johnson & Johnson Healthcare Products Division of McNEIL-PPC, Inc. | |||||||||||||
Full Title: A PHASE 3 MULTI-CENTER PARALLEL DESIGN CLINICAL TRIAL TO COMPARE THE EFFICACY AND SAFETY OF 5% MINOXIDIL FOAM VS. VEHICLE IN FEMALES FOR THE TREATMENT OF FEMALE PATTERN HAIR LOSS (ANDROGENETIC ALOP... | |||||||||||||
Medical condition: FEMALE PATTERN HAIR LOSS (ANDROGENETIC ALOPECIA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012226-37 | Sponsor Protocol Number: PIOMET-55 | Start Date*: 2010-01-15 |
Sponsor Name:HOSPITAL SANT JOAN DE DÉU | ||
Full Title: Ensayo clínico piloto de tratamiento con Pioglitazona+Flutamida+Metformina a Dosis Bajas versus Etinil-Estradiol + Acetato de Ciproterona como control, en Adolescentes con Hiperandrogenismo Ovárico... | ||
Medical condition: Hiperandrogenismo ovárico asociado a hiperinsulinismo. | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003585-34 | Sponsor Protocol Number: METRO | Start Date*: 2006-08-28 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: WEEKLY DOCETAXEL COMBINED WITH DAILY ORAL LOW DOSES OF PREDNISONE AND CYCLOPHOSPHAMIDE IN HORMONE-REFRACTORY PROSTATE CARCINOMA A PHASE I/II STUDY | |||||||||||||
Medical condition: hormone refractory prostate carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000248-23 | Sponsor Protocol Number: C3441052 | Start Date*: 2021-10-22 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: TALAPRO-3: A PHASE 3, RANDOMIZED, DOUBLE-BLIND, STUDY OF TALAZOPARIB WITH ENZALUTAMIDE VERSUS PLACEBO WITH ENZALUTAMIDE IN MEN WITH DDR GENE MUTATED METASTATIC CASTRATION-SENSITIVE PROSTATE CANCER | |||||||||||||
Medical condition: Metastatic Castration-sensitive Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Ongoing) DE (Ongoing) NO (Ongoing) SK (Ongoing) FI (Ongoing) BE (Ongoing) NL (Ongoing) ES (Ongoing) BG (Ongoing) HU (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-006050-51 | Sponsor Protocol Number: RD.06.SPR.202395 | Start Date*: 2021-08-03 | |||||||||||
Sponsor Name:Galderma S.A. | |||||||||||||
Full Title: Evaluation of the risk of atrophic acne scar formation during treatment of acne vulgaris subjects with trifarotene 50 µg/g cream versus vehicle cream over 24 weeks | |||||||||||||
Medical condition: acne vulgaris | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003494-22 | Sponsor Protocol Number: ANB019-207 | Start Date*: 2021-02-24 | |||||||||||
Sponsor Name:AnaptysBio Inc. | |||||||||||||
Full Title: A Phase 2a, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ANB019 in the Treatment of Acneiform Rash in Subjects with Cancer Receiving EGFRi or MEKi Therapy | |||||||||||||
Medical condition: Acneiform Rash | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) CZ (Prematurely Ended) LV (Prematurely Ended) BG (Prematurely Ended) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000193-31 | Sponsor Protocol Number: PR08 | Start Date*: 2004-10-04 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name: University College London | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Systemic Therapy in Advancing or Metastatic Prostate Cancer: Evaluation of Drug Efficacy | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Prostate Cancer | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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