- Trials with a EudraCT protocol (48)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
48 result(s) found for: Stage IIIA Breast Cancer.
Displaying page 1 of 3.
EudraCT Number: 2009-018148-45 | Sponsor Protocol Number: H3E-EW-JMIP | Start Date*: 2010-10-20 | ||||||||||||||||
Sponsor Name:Eli Lilly and Company Limited | ||||||||||||||||||
Full Title: An exploratory Phase 2 study of Pemetrexed and Cisplatin as Preoperative chemotherapy in the treatment of Stage IIIAN2 nonsquamous non-Small cell lung cancer | ||||||||||||||||||
Medical condition: Non Squamous Non Small Cell Lung Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011739-11 | Sponsor Protocol Number: H3E-EW-S128 | Start Date*: 2009-08-04 | ||||||||||||||||
Sponsor Name:Eli Lilly and Company Limited | ||||||||||||||||||
Full Title: Phase 2 Study of Pemetrexed and Cisplatin as Induction, Followed by Pemetrexed and Cisplatin with Concurrent Thoracic Radiotherapy, in Patients with Unresectable Locally-Advanced Stage III, Non-Squ... | ||||||||||||||||||
Medical condition: Non-small Cell Lung Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) ES (Completed) IT (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-001170-32 | Sponsor Protocol Number: H3E-MC-JMIG | Start Date*: 2008-09-05 | ||||||||||||||||
Sponsor Name:Eli Lilly and Company limited | ||||||||||||||||||
Full Title: Protocol H3E-MC-JMIG Phase 3 Study of Pemetrexed, Cisplatin, and Radiotherapy Followed by Consolidation Pemetrexed versus Etoposide, Cisplatin, and Radiotherapy Followed by Consolidation Cytoto... | ||||||||||||||||||
Medical condition: patients with locally advanced, unresectable/inoperable, Stage III, nonsquamous NSCLC without malignant pleural/pericardial effusion | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PT (Completed) HU (Completed) ES (Completed) NL (Completed) BE (Completed) FR (Completed) DE (Completed) GB (Completed) IE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000662-65 | Sponsor Protocol Number: D5164C00001 | Start Date*: 2015-08-12 | |||||||||||||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||
Full Title: A Phase III, double-blind, randomized, placebo-controlled multi-centre, study to assess the efficacy and safety of AZD9291 versus Placebo, in patients with Epidermal Growth Factor Receptor Mutation... | |||||||||||||||||||||||
Medical condition: Stage IB-IIIA non-small cell lung carcinoma, with a centrally confirmed, common sensitising EGFR mutations (Ex19del and L858R either alone or in combination with other EGFR mutations), following co... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Trial now transitioned) IT (Completed) DE (Trial now transitioned) HU (Completed) NL (Ongoing) FR (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) SE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003912-72 | Sponsor Protocol Number: H3E-MC-S103a | Start Date*: 2007-10-31 | ||||||||||||||||
Sponsor Name:Eli Lilly and Company Limited | ||||||||||||||||||
Full Title: A Randomized Phase 2 Study Comparing Erlotinib-Pemetrexed, Pemetrexed alone, and Erlotinib alone, as Second-Line Treatment for Non-Smoker Patients with Locally Advanced or Metastatic Non-Small Cell... | ||||||||||||||||||
Medical condition: Patients with histological or cytological diagnosis of nonsquamous NSCLC with locally advanced or metastatic disease. Patients must have failed only one prior chemotherapy regimen and must be consi... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003417-14 | Sponsor Protocol Number: GEICAM 2006-10 | Start Date*: 2007-09-14 | |||||||||||
Sponsor Name:Grupo Español de Investigación en Cáncer de Mama (GEICAM) | |||||||||||||
Full Title: Ensayo fase III aleatorizado, multicéntrico, abierto, de grupos paralelos para comparar la eficacia y tolerabilidad de Fulvestrant (Faslodex®) durante tres años en combinación con Anastrozol (Arimi... | |||||||||||||
Medical condition: Postmenopausal women with operable breast cancer and positive hormonal receptors who are eligible to be treated with adjuvant hormonotherapy. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018389-22 | Sponsor Protocol Number: LAP113957 / SOLTI-1001 | Start Date*: 2010-09-07 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A randomized, multicentre, open-label, Phase II study of the efficacy and safety of lapatinib plus epirubicin and cyclophosphamide (EC90-L) followed by weekly paclitaxel and lapatinib (PX-L) compar... | |||||||||||||
Medical condition: patients with previously untreated ErbB2-overexpressing Stage I - IIIA invasive breast cancer with primary tumour size > 1cm. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) AT (Prematurely Ended) FR (Completed) NO (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004950-10 | Sponsor Protocol Number: H3E-CR-S111 | Start Date*: 2008-01-28 | |||||||||||||||||||||
Sponsor Name:Lilly S.A. | |||||||||||||||||||||||
Full Title: Pemetrexed con suplemento simplificado de folato y dexametasona frente a pemetrexed con suplemento estándar como segunda línea de quimioterapia en pacientes con cáncer de pulmón no microcítico Pe... | |||||||||||||||||||||||
Medical condition: Pacientes con cancer de pulmon no microcitico con enfermedad localmente avanzada o metastásica (estadios IIIA, IIIB o IV). | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002662-40 | Sponsor Protocol Number: AS.T.R.O.BC01-13 | Start Date*: 2013-09-10 | |||||||||||
Sponsor Name:AS.T.R.O. | |||||||||||||
Full Title: PERtuzumab-trastuzumab plus lEetrozoLe In endocrine Sensitive breast cancer: a phase II neoAdjuvant study | |||||||||||||
Medical condition: Stage II-IIIA operable breast cancer, HER2 positive and hormone receptor-positive, previously untreated | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000418-31 | Sponsor Protocol Number: IKP275 | Start Date*: 2019-04-01 | ||||||||||||||||||||||||||
Sponsor Name:Robert Bosch Gesellschaft für medizinische Forschung mbH | ||||||||||||||||||||||||||||
Full Title: GENOTYPE AND PHENOTYPE GUIDED SUPPLEMENTATION OF TAMOXIFEN STANDARD THERAPY WITH ENDOXIFEN IN BREAST CANCER PATIENTS. | ||||||||||||||||||||||||||||
Medical condition: Patients with ductal carcinoma in situ (DCIS) or early stage breast cancer. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005173-56 | Sponsor Protocol Number: GOG/2007-01 | Start Date*: 2008-03-06 | |||||||||||
Sponsor Name:Grupo Oncológico Gallego (GOG) | |||||||||||||
Full Title: ENSAYO CLÍNICO ABIERTO, NO ALEATORIZADO, EN FASE II, DE TRATAMIENTO SECUENCIAL CON TAXOTERE® (T) SEGUIDO DE MYOCET® Y CICLOFOSFAMIDA (MC), COMO TRATAMIENTO ANTINEOPLASICO PRIMARIO EN PACIENTES CON ... | |||||||||||||
Medical condition: Cáncer de mama localizado (estadio II y IIIa). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000251-18 | Sponsor Protocol Number: PO4572 | Start Date*: 2006-05-12 |
Sponsor Name:Dr. Llombart Cussac | ||
Full Title: Phase II Cardiac Safety trial of liposomal pegillated doxorrubicine in patients with breast cancer with non evidence of disease and previous exposition to Antraciclines. Estudio Fase II de Seguri... | ||
Medical condition: Non evidence of disease (NED) Breast cancer. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002600-33 | Sponsor Protocol Number: IBCSG 34-05/ SWOG 0230 | Start Date*: 2007-02-16 | |||||||||||
Sponsor Name:International Breast Cancer Study Group (IBCSG) | |||||||||||||
Full Title: Phase III trial of LHRH analog administration during chemotherapy to reduce ovarian failure following chemotherapy in early stage, hormone-receptor negative breast cancer | |||||||||||||
Medical condition: Premenopausal women, Early Stage I, II or IIIA, ER-/ PR- Breast Cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) IT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011756-22 | Sponsor Protocol Number: ICARO 2 | Start Date*: 2009-10-05 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI CAGLIARI | |||||||||||||
Full Title: Reinduction with liposomal anthracyclines and Capecitabine in patients with breast cancer, locally advanced (IIIA-IIIB-IIIC) HER2 negative, not obtaining a pathological complete response ( | |||||||||||||
Medical condition: Population of female patients suffering from breast cancer in initial clinical stage IIIA, IIIB and IIIC not expressing HER2 and who have not obtained a pathological complete response (defined | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002493-13 | Sponsor Protocol Number: M16BRC | Start Date*: 2016-09-15 | |||||||||||
Sponsor Name:NKI-AVL | |||||||||||||
Full Title: Substantially improving the cure rate of high-risk BRCA1-like breast cancer patients with personalized therapy | |||||||||||||
Medical condition: High risk breast cancer (stage III), BRCA1-like | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001649-34 | Sponsor Protocol Number: CNIO-BR-01-2010/GEICAM/2010-10 | Start Date*: 2011-09-19 | |||||||||||
Sponsor Name:CNIO - Centro Nacional de Investigaciones Oncológicas | |||||||||||||
Full Title: Ensayo clínico de fase I/II, aleatorizado, de paclitaxel neoadyuvante frente a imprimación con BIBF 1120 seguida por BIBF 1120 más paclitaxel en cáncer de mama HER-2 negativo con estudios correlati... | |||||||||||||
Medical condition: Pacientes con cáncer de mama localizado (estadios II y IIIA) confirmado histológicamente. Patients histologically confirmed localized breast cancer (stage II and IIIA). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003029-16 | Sponsor Protocol Number: GO29505 | Start Date*: 2014-12-01 | |||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||
Full Title: A phase II randomized, double-blind study of ipatasertib (GDC-0068), an inhibitor to Akt in combination with paclitaxel as neoadjuvant treatment for patients with early stage triple negative breast... | |||||||||||||
Medical condition: Early stage triple negative breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001036-22 | Sponsor Protocol Number: SOLTI-1114 | Start Date*: 2013-10-15 | |||||||||||
Sponsor Name:SOLTI | |||||||||||||
Full Title: PAM50 HER2-enriched phenotype as a predictor of early response to neoadjuvant lapatinib plus trastuzumab in Stage I to IIIA HER2-positive breast cancer | |||||||||||||
Medical condition: Untreated invasive breast carcinoma eligible for primary definitive surgery (Stage I-IIIA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018960-17 | Sponsor Protocol Number: TCD11419 | Start Date*: 2010-06-16 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: "Estudio de fase II, abierto, aleatorizado para evaluar la eficacia y seguridad de paclitaxel administrado semanalmente como agente único y dos regímenes diferentes de SAR240550 (BSI-201), un inhib... | |||||||||||||
Medical condition: Neoadyuvante en pacientes con cáncer de mama triple negativo en estadio II-IIIA (TNBC) _______________________________________________ Neoadjuvant TNBC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) FR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010000-28 | Sponsor Protocol Number: BP22572 | Start Date*: 2009-08-24 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: An open-label, multi-center study of the safety and tolerability of the combination of Trastuzumab-MCC-DM1 (T-DM1) with docetaxel, and potentially pertuzumab, for treatment for patients with advanc... | ||||||||||||||||||
Medical condition: Treatment in patients with advanced, HER2-positive breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
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