- Trials with a EudraCT protocol (33)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
33 result(s) found for: Toremifene.
Displaying page 1 of 2.
EudraCT Number: 2006-006109-97 | Sponsor Protocol Number: TORE 20 | Start Date*: 2007-02-20 | |||||||||||
Sponsor Name:Sinikka Oksa | |||||||||||||
Full Title: THE EFFECT OF TOREMIFENE TO THE FINDINGS OF MAGNETIC RESONANCE IMAGING IN WOMEN WITH PREMENSTRUAL MASTALGIA | |||||||||||||
Medical condition: PREMENSTRUAL MASTALGIA | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006205-95 | Sponsor Protocol Number: 2011-006205-95 | Start Date*: 2012-10-05 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
Full Title: Toremifene in desmoid tumor: prospective clinical trial and identification of potential molecular targets | |||||||||||||
Medical condition: Primary or recurrent sporadic desmoid tumor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016948-39 | Sponsor Protocol Number: tore5 | Start Date*: 2010-08-02 |
Sponsor Name:Sinikka Oksa | ||
Full Title: Toremifeenihoidon vaikutus rintojen 3D-ultraäänilöydökseen | ||
Medical condition: Tutkittavat ovat terveitä naisia iältään 20-45vuotta. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002371-16 | Sponsor Protocol Number: D6997C00002 (9238IL/0064) | Start Date*: 2004-11-18 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Randomised, Double-Blind, Parallel-group, Multicentre, Phase III Study Comparing the Efficacy and Tolerability of Fulvestrant (FASLODEX™) 500 mg with Fulvestrant (FASLODEX™) 250 mg in Postmenopau... | ||
Medical condition: Postmenopausal women with advanced breast cancer, progressing or relapsing after previous endocrine therapy | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: SK (Completed) CZ (Completed) HU (Completed) ES (Completed) IT (Completed) MT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004247-54 | Sponsor Protocol Number: D6997C00006 (9238IL/0068) | Start Date*: 2006-04-05 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Randomised, Double-blind, Parallel-group, Multicentre, Phase II Study to Evaluate the Efficacy and Tolerability of Fulvestrant (FASLODEX™) 250 mg, Fulvestrant (FASLODEX™) 250 mg (plus 250 mg Load... | ||
Medical condition: Postmenopausal women with oestrogen receptor (ER) positive advanced breast cancer who have either relapsed whilst on adjuvant endocrine therapy, or progressed whilst on first endocrine therapy for ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) HU (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002990-24 | Sponsor Protocol Number: RAD1901-308 | Start Date*: 2019-05-29 | |||||||||||
Sponsor Name:Stemline Therapeutics, Inc. | |||||||||||||
Full Title: Elacestrant Monotherapy vs. Standard of Care for the Treatment of Patients with ER+/HER2- Advanced Breast Cancer Following CDK4/6 Inhibitor Therapy: A Phase 3 Randomized, Open-Label, Active-Control... | |||||||||||||
Medical condition: Advanced breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Ongoing) HU (Completed) AT (Completed) GR (Completed) IE (Completed) PT (Completed) DK (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003467-19 | Sponsor Protocol Number: CLEE011A2404 | Start Date*: 2016-12-08 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: COMPLEEMENT-1: An open-label, multicenter, Phase IIIb study to assess the safety and efficacy of ribociclib (LEE011) in combination with letrozole for the treatment of men and pre/postmenopausal wo... | |||||||||||||
Medical condition: hormone receptor-positive (HR+) HER2-negative (HER2-) advanced breast cancer (aBC) with no prior hormonal therapy for advanced disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) NL (Completed) HU (Completed) BG (Completed) PT (Completed) GR (Completed) SK (Completed) IT (Completed) CZ (Completed) AT (Completed) ES (Completed) DK (Completed) NO (Completed) PL (Completed) FI (Completed) SI (Completed) RO (Ongoing) LU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002176-39 | Sponsor Protocol Number: V3002401 | Start Date*: 2022-02-07 | |||||||||||
Sponsor Name:Veru Inc. | |||||||||||||
Full Title: ARTEST - A Randomized Phase 3 Study to Evaluate the Efficacy and Safety of Enobosarm Monotherapy Versus Active Control for the Treatment of AR+/ER+/HER2- Metastatic Breast Cancer in Patients with A... | |||||||||||||
Medical condition: (AR+)/estrogen receptor positive(ER+)/human epidermal growth factor receptor 2 negative (HER2-) metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001213-32 | Sponsor Protocol Number: MedOPP168 | Start Date*: 2019-02-04 | |||||||||||
Sponsor Name:Medica Scientia Innovation Research (MedSIR) | |||||||||||||
Full Title: Effectiveness of olaparib plus trastuzumab in HER2-positive BRCA-mutated or Homologous Recombination Deficiency (HRD) advanced breast cancer patients – The OPHELIA Study – | |||||||||||||
Medical condition: HER2-positive BRCAmutated or Homologous Recombination Deficiency (HRD) advanced breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000365-37 | Sponsor Protocol Number: MIN-003-1806 | Start Date*: 2019-06-04 | |||||||||||
Sponsor Name:Lipopharma Therapeutics | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled adjuvant trial in newly diagnosed primary glioblastoma subjects to assess the efficacy and safety of 2-hydroxyoleic acid (2-OHOA) in combination with ... | |||||||||||||
Medical condition: Newly diagnosed primary glioblastoma multiforme (ndGBM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) GB (GB - no longer in EU/EEA) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000055-39 | Sponsor Protocol Number: TACTI-003 | Start Date*: 2021-12-21 | |||||||||||
Sponsor Name:Immutep S.A.S. | |||||||||||||
Full Title: TACTI-003 (Two ACTive Immunotherapeutics): A multicenter, open label, randomized, Phase II trial to investigate a soluble LAG-3 fusion protein, eftilagimod alpha (efti; IMP321) in combination with ... | |||||||||||||
Medical condition: Metastatic head and neck squamous cell carcinoma (HNSCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) DE (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002541-63 | Sponsor Protocol Number: IMP321-P011 | Start Date*: 2015-12-21 | ||||||||||||||||
Sponsor Name:Immutep S.A.S. | ||||||||||||||||||
Full Title: AIPAC (Active Immunotherapy PAClitaxel): A multicentre, Phase IIb, randomised, double blind, placebo-controlled study in hormone receptor-positive metastatic breast carcinoma patients receiving IMP... | ||||||||||||||||||
Medical condition: Female metastasized oestrogen receptor positive and/or progesterone receptor positive breast adenocarcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: NL (Completed) BE (Completed) HU (Completed) FR (Completed) DE (Completed) PL (Completed) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002113-39 | Sponsor Protocol Number: BAY88-8223/16298 | Start Date*: 2014-10-29 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: A phase II randomized, double-blind, placebo-controlled trial of radium-223 dichloride versus placebo when administered to metastatic HER2 negative hormone receptor positive breast cancer subjects ... | |||||||||||||
Medical condition: HER2 negative hormone receptor positive metastatic breast cancer with bone metastases treated with standard of care hormonal treatment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) AT (Completed) NO (Completed) CZ (Completed) DK (Prematurely Ended) NL (Completed) SE (Completed) PL (Completed) FI (Completed) IE (Completed) FR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006326-24 | Sponsor Protocol Number: D699BC00001 | Start Date*: 2012-11-07 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Randomised, Double-blind, Parallel-group, Multicentre, Phase III Study to Compare the Efficacy and Tolerability of Fulvestrant (FASLODEX) 500 mg with Anastrozole (ARIMIDEX) 1 mg as Hormonal Treat... | ||
Medical condition: hormone receptor positive breast cancer, hormone naive, breast, cancer, neoplasm breast cancer, metastatic, tumour, neoplasm | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) CZ (Completed) SK (Completed) IT (Completed) PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004324-30 | Sponsor Protocol Number: MedOPP167 | Start Date*: 2019-02-04 | ||||||||||||||||
Sponsor Name:Medica Scientia Innovation Research (MEDSIR) | ||||||||||||||||||
Full Title: A multicenter, randomized, phase II trial evaluating the efficacy of eribulin monotherapy and eribulin plus endocrine therapy in locally- recurrent or metastatic breast cancer patients after progre... | ||||||||||||||||||
Medical condition: Luminal Metastatic Breast Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005067-40 | Sponsor Protocol Number: IBCSG_55-17 | Start Date*: 2019-01-08 | ||||||||||||||||
Sponsor Name:ETOP IBCSG Partners Foundation | ||||||||||||||||||
Full Title: Phase II open-label, multicenter, randomized trial of neoadjuvant palbociclib in combination with hormonal therapy and HER2 blockade versus paclitaxel in combination with HER2 blockade for postmeno... | ||||||||||||||||||
Medical condition: Postmenopausal women with histologically confirmed estrogen receptor positive, HER2 positive primary breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: BE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-004899-19 | Sponsor Protocol Number: UC-BCG-1911 | Start Date*: 2020-06-09 |
Sponsor Name:UNICANCER | ||
Full Title: Adjuvant PalbOciclib + LetrOzole combination for hormone receptor positive / HER2-negative, Intermediate Risk breast cancer | ||
Medical condition: Hormone receptor (HR) positive / HER2-negative localized breast cancer in menopausal patient considered as having an intermediate risk of relapse. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000845-42 | Sponsor Protocol Number: CBYL719A0HR01T | Start Date*: 2022-04-04 |
Sponsor Name:CCGCRO | ||
Full Title: Impact of time of alpelisib administration, concomitant fasting and low carbohydrate diet on alpelisib toxicity and efficacy; a pilot randomized controlled phase IIb trial - ITACA | ||
Medical condition: metastatic breast cancer HER2- HR+ PIK3CA+ | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HR (Suspended by CA) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003131-11 | Sponsor Protocol Number: 1280-0022 | Start Date*: 2018-12-11 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: XeneraTM-1: A multi-centre, double-blind, placebo-controlled, randomised phase II trial to compare efficacy of xentuzumab in combination with everolimus and exemestane versus everolimus and exemest... | |||||||||||||
Medical condition: HR+ / HER2- metastatic breast cancer and non-visceral disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) ES (Completed) GR (Completed) PT (Prematurely Ended) GB (GB - no longer in EU/EEA) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001994-25 | Sponsor Protocol Number: TACTI-002(IMP321P015);KeynotePN798 | Start Date*: 2019-02-12 | ||||||||||||||||||||||||||
Sponsor Name:Immutep S.A.S. | ||||||||||||||||||||||||||||
Full Title: TACTI-002 (Two ACTive Immunotherapeutics): A multicenter, open label, Phase II study in patients with previously untreated unresectable or metastatic non-small cell lung cancer (NSCLC), or recurren... | ||||||||||||||||||||||||||||
Medical condition: Previously untreated unresectable or metastatic non-small cell lung cancer (NSCLC), or recurrent PD-X refractory NSCLC or recurrent or metastatic squamous head and neck cancer (HNSCC) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) PL (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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