- Trials with a EudraCT protocol (196)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
196 result(s) found for: Reproductive neoplasms male benign.
Displaying page 1 of 10.
| EudraCT Number: 2019-001559-38 | Sponsor Protocol Number: GEICAM/2018-06 | Start Date*: 2022-01-20 | ||||||||||||||||
| Sponsor Name:GEICAM (Fundación Grupo Español de Investigación en Cáncer de Mama) | ||||||||||||||||||
| Full Title: A Randomized Phase II Study to Evaluate the Incidence of Discontinuations due to Diarrhoea at 3 Cycles in patients with Early-stage HER2-positive (HER2+), Hormone Receptor-positive (HR+) Breast Can... | ||||||||||||||||||
| Medical condition: HER2+, HR+ Early stage Breast Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) FR (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-001988-52 | Sponsor Protocol Number: 90101 | Start Date*: 2012-07-30 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:EORTC | ||||||||||||||||||||||||||||||||||||||
| Full Title: Cross-tumoral Phase 2 clinical trial exploring Crizotinib (PF-02341066) in patients with advanced tumours induced by causal alterations of either ALK or MET. | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Locally advanced and/or metastatic malignant tumor (anaplastic large cell lymphoma, inflammatory myofibroblastic tumor, papillary renal cell carcinoma type 1, alveolar soft part sarcoma, clear cell... | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) NL (Completed) FR (Completed) NO (Completed) SI (Prematurely Ended) IT (Completed) PL (Completed) DK (Prematurely Ended) SK (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-000192-20 | Sponsor Protocol Number: PL3397-A-U4003 | Start Date*: 2020-07-22 | |||||||||||
| Sponsor Name:DAIICHI SANKYO, INC. | |||||||||||||
| Full Title: A Phase 4, multicenter study to evaluate the discontinuation and re treatment in subjects with tenosynovial giant cell tumor (TGCT) previously treated with pexidartinib | |||||||||||||
| Medical condition: Tenosynovial giant cell tumor (TGCT) is a group of neoplasms including pigmented villonodular synovitis (PVNS) and giant cell tumor of the tendon sheath (GCT-TS) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) NL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001896-35 | Sponsor Protocol Number: PUMA-NER-6203 | Start Date*: 2020-01-30 | |||||||||||||||||||||||||||||||
| Sponsor Name:Puma Biotechnology, Inc | |||||||||||||||||||||||||||||||||
| Full Title: An Open-Label Phase 2 Study to Characterize Colon Pathology in Patients With HER2 Amplified Breast Cancer Treated With Neratinib | |||||||||||||||||||||||||||||||||
| Medical condition: HER2 amplified (HER2+) stage 1 through stage 4 primary adenocarcinoma of the breast | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: PT (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-001063-36 | Sponsor Protocol Number: eNERGY | Start Date*: 2016-06-16 | |||||||||||
| Sponsor Name:CHU Rennes | |||||||||||||
| Full Title: Randomised phase III study testing nivolumab versus chemotherapy in first line treatment of PS 2 or elderly (more than 70 years old) patients with advanced non-small cell lung cancer | |||||||||||||
| Medical condition: Advanced non small cell lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-003424-76 | Sponsor Protocol Number: CTX-SPL9111-001 | Start Date*: 2018-01-30 | |||||||||||
| Sponsor Name:Starpharma Pty Ltd | |||||||||||||
| Full Title: A phase 1/2 dose-escalation study to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of CTX-SPL9111 (a cabazitaxel (CTX)-dendrimer conjugate) in patients with advanced ... | |||||||||||||
| Medical condition: Patients with advanced solid tumours | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000877-19 | Sponsor Protocol Number: DTX-SPL8783-001 | Start Date*: 2016-07-13 | |||||||||||
| Sponsor Name:Starpharma Pty Ltd. | |||||||||||||
| Full Title: A phase 1/2 dose-escalation study to evaluate the safety, tolerability, and pharmacokinetics and preliminary efficacy of DTX-SPL8783 (a docetaxel (DTX)-dendrimer conjugate) as monotherapy in patien... | |||||||||||||
| Medical condition: Locally advanced, metastatic or locally recurrent non-small cell lung cancer (NSCLC). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002842-60 | Sponsor Protocol Number: eNERGY | Start Date*: 2017-09-14 | |||||||||||
| Sponsor Name:CHU Rennes | |||||||||||||
| Full Title: Randomised phase III study testing nivolumab and ipilimumab versus a carboplatin based doublet in first line treatment of PS 2 or elderly (more than 70 years old) patients with advanced non-small... | |||||||||||||
| Medical condition: Advanced non small cell lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-000758-20 | Sponsor Protocol Number: DIV-SCLC-301 | Start Date*: 2017-06-21 | |||||||||||
| Sponsor Name:United Therapeutics Corporation | |||||||||||||
| Full Title: A Two-Part, Open-Label, Randomized, Phase II/III Study of Dinutuximab and Irinotecan versus Irinotecan for Second Line Treatment of Subjects with Relapsed or Refractory Small Cell Lung Cancer | |||||||||||||
| Medical condition: relapsed or refractory small cell lung cancer (SCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) HU (Completed) BG (Completed) LT (Completed) FR (Completed) PL (Completed) SK (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001896-35 | Sponsor Protocol Number: ETOP3-12 | Start Date*: 2012-08-29 | |||||||||||
| Sponsor Name:ETOP (European Thoracic Oncology Platform) | |||||||||||||
| Full Title: A randomized phase III trial of erlotinib versus docetaxel in patients with advanced squamous cell non-small cell lung cancer who failed first line platinum based doublet chemotherapy stratified by... | |||||||||||||
| Medical condition: Squamous cell non-small cell lung cancer in patients who have failed first-line platinum-based doublet chemotherapy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) HU (Completed) IE (Completed) AT (Completed) ES (Completed) NL (Prematurely Ended) DE (Completed) IT (Completed) DK (Prematurely Ended) GB (Completed) GR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001989-10 | Sponsor Protocol Number: CPI0610-04 | Start Date*: 2021-01-08 | ||||||||||||||||||||||||||
| Sponsor Name:Constellation Pharmaceuticals, Inc. | ||||||||||||||||||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind, Active-Control Study of CPI-0610 and Ruxolitinib vs. Placebo and Ruxolitinib in JAKi Treatment Naive MF Patients | ||||||||||||||||||||||||||||
| Medical condition: Myelofibrosis | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) HU (Completed) DE (Trial now transitioned) AT (Trial now transitioned) PL (Trial now transitioned) CZ (Trial now transitioned) NL (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2015-004984-35 | Sponsor Protocol Number: EZH-501 | Start Date*: 2016-08-03 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Epizyme, Inc. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Tazemetostat Rollover Study (TRuST): An Open-Label, Rollover Study | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Subjects will receive tazemetostat as dictated in their antecedent study. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) PL (Trial now transitioned) BE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-004436-61 | Sponsor Protocol Number: BRF113771 | Start Date*: 2012-03-30 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research and Development Limited | |||||||||||||
| Full Title: A Four-Part, Open-Label Study to Evaluate the Effects of Repeat Dose GSK2118436 on the Single Dose Pharmacokinetics of Warfarin, the Effects of Repeat Dose Oral Ketoconazole and Oral Gemfibrozil on... | |||||||||||||
| Medical condition: Skin Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005151-27 | Sponsor Protocol Number: PREMITO2015 | Start Date*: 2016-05-06 | ||||||||||||||||
| Sponsor Name:Hospital Universitario de Canarias | ||||||||||||||||||
| Full Title: Randomized prospective clinical trial to evaluate the rate of early recurrence in bladder cancer in non-muscle invasive between the chemohyperthermia (QH) with mitomycin-C prior to transurethral re... | ||||||||||||||||||
| Medical condition: | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-004483-22 | Sponsor Protocol Number: D967LC00001 | Start Date*: 2020-09-09 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Phase 1b/2 Multicenter, Open-label, Dose-escalation and Dose expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Antitumor Activity of Trastuzumab Deruxtec... | |||||||||||||
| Medical condition: Patients with Human Epidermal Growth Factor Receptor 2 (HER2)-expressing gastric, GEJ and esophageal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) DE (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-002093-12 | Sponsor Protocol Number: 1506-STBSG | Start Date*: 2017-07-04 | ||||||||||||||||
| Sponsor Name:European Organisation for Research and Treatment of | ||||||||||||||||||
| Full Title: A Phase II multicenter study comparing the efficacy of the oral angionenesis inhibitor nintedanib with the intravenous cytotoxis compound ifosfamide for treatment of patients with advanced metastat... | ||||||||||||||||||
| Medical condition: Metastatic soft tissue sarcoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) PL (Completed) NL (Completed) ES (Completed) LT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-002214-38 | Sponsor Protocol Number: VAROCE-1206 | Start Date*: 2013-01-18 | ||||||||||||||||
| Sponsor Name:Centre Oscar Lambret | ||||||||||||||||||
| Full Title: A PHASE II RANDOMIZED STUDY OF DOCETAXEL WITH OR WITHOUT NINTEDANIB (BIBF-1120) IN PATIENT RECEIVING A SECOND-LINE OF CHEMOTHERAPY FOR HER NEGATIVE, METASTATIC OR LOCALLY RECURRENT BREAST CANCER | ||||||||||||||||||
| Medical condition: Second-line chemotherapy for metastatic or locally recurrent breast cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-002553-29 | Sponsor Protocol Number: kk-2013 | Start Date*: 2013-08-22 | ||||||||||||||||||||||||||
| Sponsor Name:Jens Sønksen | ||||||||||||||||||||||||||||
| Full Title: Metabolic changes due to iatrogenic hypogonadism in patients with prostate cancer: orchiectomy vs. triptorelin | ||||||||||||||||||||||||||||
| Medical condition: Men with prostate cancer where lifelong castration is indicated | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2021-004631-92 | Sponsor Protocol Number: WWU20_0041 | Start Date*: 2022-07-26 | |||||||||||
| Sponsor Name:Westfälische Wilhelms-Universität Münster, C/o Universitätsklinikum Münster Geschäftsbereich Recht u. Drittmittel | |||||||||||||
| Full Title: Phase I/II dose escalation trial of radiodynamic therapy (RDT) with 5-Aminolevulinic acid in patients with first recurrence of glioblastoma | |||||||||||||
| Medical condition: recurrence of glioblastoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-014383-18 | Sponsor Protocol Number: CRAD001CDE21T | Start Date*: 2010-08-12 | |||||||||||
| Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
| Full Title: A single arm, open-label multicenter phase II trial of everolimus in patients with relapsed/refractory germ cell cancer | |||||||||||||
| Medical condition: Germ cell tumor, metastatic, relapsed or refractory | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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