- Trials with a EudraCT protocol (102)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
102 result(s) found for: Ki-67.
Displaying page 1 of 6.
EudraCT Number: 2014-005508-62 | Sponsor Protocol Number: TRINACRIA | Start Date*: 2015-10-08 | ||||||||||||||||
Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | ||||||||||||||||||
Full Title: A phase II, randomized, non-comparative, pre-surgical study of atorvastatin or observation in Ki-67 positive, TAZ-expressing early breast cancer patients | ||||||||||||||||||
Medical condition: Early breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005792-12 | Sponsor Protocol Number: GOIRC-06-2020 | Start Date*: 2022-04-05 | |||||||||||
Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA CLINICA (GOIRC) | |||||||||||||
Full Title: Pilot ‘Window of Opportunity’ Neoadjuvant Study of Abemaciclib in Low-Estrogen Receptor (ER) positive/Human Epidermal Growth Factor Receptor 2 (HER2)-negative Early Breast Cancer (BC) | |||||||||||||
Medical condition: Low-Estrogen Receptor (ER) positive/Human Epidermal Growth Factor Receptor 2 (HER2)-negative Early Breast Cancer (BC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003906-81 | Sponsor Protocol Number: A7-2 | Start Date*: 2005-01-14 |
Sponsor Name:Oncology Institute of Vilnius University | ||
Full Title: Chemoradiation with once weekly gemcitabine for invasive bladder cancer | ||
Medical condition: Invasive transitional cell bladder cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006542-34 | Sponsor Protocol Number: PR3076 | Start Date*: 2007-01-08 |
Sponsor Name:Pantarhei Bioscience B.V. | ||
Full Title: Preoperative hormone therapy for pre- and postmenopausal women with ER positive breast cancer: A double blind randomized parallel group phase II trial, comparing the effect of 2 weeks of preoperati... | ||
Medical condition: breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001651-40 | Sponsor Protocol Number: Phaon1 | Start Date*: 2020-11-13 | |||||||||||
Sponsor Name:palleos healthcare GmbH | |||||||||||||
Full Title: An adaptive randomized neoadjuvant two arm trial in triple-negative breast cancer comparing a mono Atezolizumab window followed by a Atezolizumab - CTX therapy with Atezolizumab – CTX therapy (neoM... | |||||||||||||
Medical condition: ER negative, PR negative and HER2 negative (triple negative) breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000476-26 | Sponsor Protocol Number: N14DAR | Start Date*: 2020-07-13 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Netherlands Cancer Institute | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Dynamics of Androgen Receptor genomics and transcriptomics after neoadjuvant androgen ablation (DARANA) | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Prostate cancer | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007652-10 | Sponsor Protocol Number: BRD 08/11-A | Start Date*: 2009-04-06 |
Sponsor Name:Centre René Gauducheau | ||
Full Title: Etude de phase II ouverte évaluant en fonction du polymorphisme du CYP2D6, le taux de réponse biologique au traitement par tamoxifène (TAM) administré en situation pré-opératoire chez des patientes... | ||
Medical condition: Cancer du sein | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001084-27 | Sponsor Protocol Number: APAC | Start Date*: 2006-06-16 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALI GALLIERA | |||||||||||||
Full Title: Phase I/II study of prevention of Colorectal Cancer CRC with Allopurinol in High-Risk Subjects | |||||||||||||
Medical condition: CHEMOPREVENTION OF COLORECTAL CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002588-24 | Sponsor Protocol Number: CLEE011A2201 | Start Date*: 2013-12-30 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: A randomized pre-surgical pharmacodynamics study to assess the biological activity of LEE011 plus letrozole versus single agent letrozole in primary breast cancer | ||
Medical condition: HR+, HER2- early breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Completed) ES (Prematurely Ended) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002947-41 | Sponsor Protocol Number: N19PCA | Start Date*: 2019-11-20 |
Sponsor Name:Netherlands Cancer Institute- Antoni van Leeuwenhoek | ||
Full Title: Neoadjuvant trial on the efficacy of propranolol monotherapy in angiosarcoma (PROPANGIO). | ||
Medical condition: Angiosarcoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001447-40 | Sponsor Protocol Number: 28UCS2019 | Start Date*: 2020-06-29 | ||||||||||||||||
Sponsor Name:ENTE OSPEDALIERO OSPEDALI GALLIERA | ||||||||||||||||||
Full Title: Pilot Study of Daily Exemestane in Women with Complex Atypical Hyperplasia of the Endometrium / Endometrial Intraepithelial Neoplasia or Low Grade Endometrial Cancer | ||||||||||||||||||
Medical condition: Complex Atypical Hyperplasia of the Endometrium / Endometrial Intraepithelial Neoplasia or Low Grade Endometrial Cancer in post-menopausal women | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018311-15 | Sponsor Protocol Number: GE-148-003 | Start Date*: 2010-05-21 |
Sponsor Name:GE Healthcare Limited | ||
Full Title: A Phase 2, Open-label Study to Assess the Uptake and Retention and Safety of GE 148 (18F) Injection in Subjects with Biopsy-proven Prostate Cancer who are Scheduled for Radical Prostatectomy | ||
Medical condition: Detection of abnormal amino acid transport using Positron Emission Tomography (PET) in malignancy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Prematurely Ended) FI (Prematurely Ended) DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004362-26 | Sponsor Protocol Number: I3Y-MC-JPCF | Start Date*: 2017-08-14 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Open-Label, Phase 3 Study of Abemaciclib Combined with Standard Adjuvant Endocrine Therapy versus Standard Adjuvant Endocrine Therapy Alone in Patients with High-Risk, Node-Positive, ... | |||||||||||||
Medical condition: Node Positive, Early Stage, Hormone Receptor Positive, Human Epidermal Receptor 2 Negative, Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) NL (Trial now transitioned) HU (Trial now transitioned) GB (GB - no longer in EU/EEA) BE (Trial now transitioned) DK (Trial now transitioned) FI (Trial now transitioned) PL (Trial now transitioned) GR (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) CZ (Trial now transitioned) FR (Trial now transitioned) PT (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003064-47 | Sponsor Protocol Number: CUDC-101-104 | Start Date*: 2012-12-11 | |||||||||||
Sponsor Name:Curis, Inc. | |||||||||||||
Full Title: A Phase 1 open-label study to investigate the pharmacodynamics, metabolomics and pharmacokinetics of CUDC-101 in subjects with HER2 positive invasive breast cancer. | |||||||||||||
Medical condition: HER2 positive breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000290-24 | Sponsor Protocol Number: I3Y-MC-JPCY | Start Date*: 2020-08-17 | ||||||||||||||||
Sponsor Name:Eli Lilly and Company | ||||||||||||||||||
Full Title: CYCLONE 1: A Phase 2 Study of Abemaciclib in Metastatic Castration-Resistant Prostate Cancer Patients Previously Treated with a Novel Hormonal Agent and Taxane-based Chemotherapy | ||||||||||||||||||
Medical condition: Metastatic Castration-Resistant Prostate Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000370-30 | Sponsor Protocol Number: 20150706 | Start Date*: 2015-11-26 |
Sponsor Name:Norrlands University Hospital | ||
Full Title: Diagnosis and follow up of neuroendocrine tumours with 68Ga-DotaToc PET/CT | ||
Medical condition: Neuroendocrine tumors | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005081-17 | Sponsor Protocol Number: ARV-471-BC-201 | Start Date*: 2023-01-20 | ||||||||||||||||
Sponsor Name:Arvinas Estrogen Receptor, Inc. (Arvinas) | ||||||||||||||||||
Full Title: An Open-Label, Randomized, Non-Comparative Phase 2 Study of ARV-471 or Anastrozole in Post-Menopausal Women With ER+/HER2– Breast Cancer in the Neoadjuvant Setting | ||||||||||||||||||
Medical condition: Post-menopausal women with ER+ HER2– breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005048-19 | Sponsor Protocol Number: IEO S268/505 | Start Date*: 2006-04-10 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: A phase II randomised study to investigate the effects of Bevacizumab on cell proliferation and on pCR in patients with locally advanced operable breast cancer | |||||||||||||
Medical condition: histologically proven primary breast cancer 2.0 cm, T2-T3 T4 a-d, N0-2, M0 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005063-16 | Sponsor Protocol Number: IEO370 | Start Date*: 2017-07-17 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: A randomized presurgical study with different schedules of exemestane in postmenopausal women with stage 0-II ER-positive breast cancer | |||||||||||||
Medical condition: Postmenopausal ER positive breast cancer, waiting for surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001938-35 | Sponsor Protocol Number: IFG-06-2019 | Start Date*: 2020-10-02 | |||||||||||
Sponsor Name:Institut für Frauengesundheit GmbH | |||||||||||||
Full Title: AIRE: – ASSESSING IMMUNORESPONSE POST ERIBULIN: ERIBULIN AND IMMUNOGENICITY IN ADVANCED BREAST CANCER – A PROSPECTIVELY RANDOMIZED PHASE IV STUDY | |||||||||||||
Medical condition: Female patients diagnosed with HER2 negative advanced breast cancer, which had received at least one previous chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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