- Trials with a EudraCT protocol (37)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
37 result(s) found for: vinorelbine tartrate.
Displaying page 1 of 2.
EudraCT Number: 2004-000963-81 | Sponsor Protocol Number: PM0259CA221B0 | Start Date*: 2004-11-15 |
Sponsor Name:Robapharm AG | ||
Full Title: A Randomised Phase II study of Oral Vinorelbine or I.V. Vinorelbine in patients with metastatic breast cancer previously treated with anthracyclines | ||
Medical condition: Treatment in metastatic breast cancer previously treated with anthracyclines | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: AT (Completed) BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-004105-16 | Sponsor Protocol Number: MO29872 | Start Date*: 2017-12-11 | ||||||||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||||||||||||
Full Title: A PHASE III, OPEN-LABEL, MULTICENTER, RANDOMIZED STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF ATEZOLIZUMAB COMPARED WITH CHEMOTHERAPY IN PATIENTS WITH TREATMENT-NAÏVE ADVANCED OR RECURRENT (STAG... | ||||||||||||||||||||||||||||
Medical condition: Non-small cell lung cancer | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) DK (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) PT (Completed) PL (Completed) ES (Ongoing) IE (Completed) BE (Completed) SK (Completed) BG (Completed) IT (Completed) RO (Ongoing) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-001904-10 | Sponsor Protocol Number: PM0259CA301J1 | Start Date*: 2004-09-15 |
Sponsor Name:Pierre Fabre Médicament represented by IRPF | ||
Full Title: Prospective randomised clinical phase III trial of (alternating IV and oral) vinorelbine plus cisplatin versus docetaxel plus cisplatin in first line chemotherapy of locally advanced or metastatic ... | ||
Medical condition: Treatment in locally advanced or metastatic non-small-lung cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) EE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2004-005135-26 | Sponsor Protocol Number: PM0259 CA304 J1 | Start Date*: 2005-05-02 |
Sponsor Name:Pierre Fabre Médicament | ||
Full Title: ORAL VINORELBINE AND CISPLATIN WITH CONCOMITANT RADIOTHERAPY FOLLOWED BY EITHER CONSOLIDATION THERAPY WITH ORAL VINORELBINE AND CISPLATIN PLUS BEST SUPPORTIVE CARE OR BEST SUPPORTIVE CARE ALONE IN ... | ||
Medical condition: Stage III Non small cell lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-003859-61 | Sponsor Protocol Number: PM0259CA232J1 | Start Date*: 2015-07-28 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: Randomized Phase II study comparing single agent oral vinorelbine administered with two different schedules in patients with Advanced Non Small Cell Lung Cancer unfit for a platinum-based chemotherapy | |||||||||||||
Medical condition: Advanced Non Small Lung Cancer unfit for a platinium-based chemotherapy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) PL (Completed) HU (Completed) CZ (Completed) DE (Completed) AT (Completed) FR (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000753-30 | Sponsor Protocol Number: PM0259CA219B0 | Start Date*: 2004-11-08 |
Sponsor Name:Pierre Fabre Ibérica S.A. as legal representative of Pierr Fabre Mèdicament | ||
Full Title: Phase II trial of oral vinorelbine in combination with capecitabine as first line therapy in women with previously untreated HER2 negative metastatic breast cancer. | ||
Medical condition: Treatment in women with previously untreated HER2 negative metastatic breast cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-000602-44 | Sponsor Protocol Number: NVB CA 03 P SP 102 B0 | Start Date*: 2004-09-28 |
Sponsor Name:Pierre Fabre Ibérica, S.A. | ||
Full Title: Ensayo clínico en fase I-II de vinorelbina oral (Navelbine) en combinación con capecitabina en tratamiento de primera línea en pacientes con cáncer de mama avanzado | ||
Medical condition: Advanced breast cancer (metastatic) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-000748-26 | Sponsor Protocol Number: PM0259CA215B0 | Start Date*: 2004-11-08 |
Sponsor Name:Pierre Fabre Ibérica, S.A. en representación de Pierre Fabre Mèdicament | ||
Full Title: Phase II trial of oral vinorelbine in combination with capecitabine and trastuzumab as first line therapy in women with previously untreated HER2 positive metastatic breast cancer. | ||
Medical condition: Treatment in women with previously untreated HER2 positive metastatic breast cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003530-16 | Sponsor Protocol Number: PM0259CA231B0 | Start Date*: 2012-11-14 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: Randomised phase II study evaluating, as first-line chemotherapy, weekly oral vinorelbine as a single-agent versus weekly paclitaxel as a single-agent in estrogen receptor positive, HER2 negative p... | |||||||||||||
Medical condition: advanced breast cancer with estrogen receptor positive and HER2 negative. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) ES (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003531-40 | Sponsor Protocol Number: PM259CA230J1 | Start Date*: 2012-12-20 | |||||||||||
Sponsor Name:Pierre Fabre Medicament | |||||||||||||
Full Title: Randomised phase II trial of oral vinorelbine and cisplatin followed by maintenance with single agent oral vinorelbine versus gemcitabine and cisplatin followed by maintenance with single agent gem... | |||||||||||||
Medical condition: First line Locally Advanced or Metastatic Non-Small-Cell Lung Cancer patients with squamous histological type | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) AT (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005205-30 | Sponsor Protocol Number: PM0259CA222B0 | Start Date*: 2006-09-06 | |||||||||||
Sponsor Name:Pierre Fabre Medicament | |||||||||||||
Full Title: Randomised phase II study of the combination of oral vinorelbine with capecitabine versus a sequential regimen of oral vinorelbine and capecitabine versus the combination of docetaxel and capecitab... | |||||||||||||
Medical condition: Patients with metastatic breast cancer previously treated with anthracyclines | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000962-11 | Sponsor Protocol Number: PM0259CA217B0 | Start Date*: 2005-03-01 |
Sponsor Name:Pierre Fabre Medicament represented by IRPF | ||
Full Title: Phase II Study of Navelbine oral and Arimidex as neo-adjuvant treatment in post-menopausal women with locally advanced breast carcinoma | ||
Medical condition: Neo-Adjuvant Treatment in Post-menopausal women with locally advanced breast carcinoma. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004987-23 | Sponsor Protocol Number: RAS-Triplet | Start Date*: 2020-05-22 |
Sponsor Name:UMC Utrecht | ||
Full Title: A Dose-Escalating Phase I/II Study in Patients with RAS-Mutated Metastatic Colorectal Cancer to Investigate Safety and Clinical Activity of the Triple Combination of: MEK-inhibitor binimetinib, Pan... | ||
Medical condition: colorectal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001992-30 | Sponsor Protocol Number: | Start Date*: 2015-04-20 | |||||||||||
Sponsor Name:University of Leicester | |||||||||||||
Full Title: A randomised controlled phase II trial of oral vinorelbine as second line therapy for patients with malignant pleural mesothelioma | |||||||||||||
Medical condition: Histologically confirmed malignant pleural mesothelioma | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003860-19 | Sponsor Protocol Number: PM0259CA233B0 | Start Date*: 2015-09-07 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: Randomised Phase II Study comparing, as first-line chemotherapy, single-agent Oral Vinorelbine administered with two different schedules in patients with Advanced Breast Cancer. | |||||||||||||
Medical condition: Advanced Breast Cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) ES (Completed) AT (Completed) HU (Completed) RO (Completed) CZ (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003361-18 | Sponsor Protocol Number: PM0259CA229J1 | Start Date*: 2013-01-24 | |||||||||||||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||||||||||||
Full Title: Phase II trial of oral vinorelbine in Locally Advanced or Metastatic Non-Small-Cell Lung Cancer (NSCLC) patients with Epidermal Growth Factor Receptor (EGFR) positive mutation after a failure to tr... | |||||||||||||||||||||||
Medical condition: Patients with: -Histologically or cytologically confirmed NSCLC (stage IIIB or IV) and -epidermal growth factor receptor (EGFR) positive mutation and -previously treated with tyrosine kinase inhibi... | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000284-17 | Sponsor Protocol Number: VinoMetro2015-007 | Start Date*: 2016-11-11 |
Sponsor Name:Universitätsmedizin Mainz | ||
Full Title: Phase II study of metronomic treatment with daily oral vinorelbine as first-line chemotherapy in patients with advanced/metastatic HR+/HER2- breast cancer resistant to endocrine therapy (VinoMetro). | ||
Medical condition: HR+/HER2- advanced/metastatic breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-007885-39 | Sponsor Protocol Number: 3144A1-2204-WW | Start Date*: 2008-05-27 | |||||||||||
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase I/II Study of HKI-272 in Combination With Vinorelbine in Subjects With Solid Tumors and Metastatic Breast Cancer. | |||||||||||||
Medical condition: Solid tumors (part 1) and metastatic breast cancer (part 2). | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) PL (Completed) FR (Completed) NL (Completed) GB (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003779-37 | Sponsor Protocol Number: IOM-080-2 | Start Date*: 2009-02-05 | |||||||||||
Sponsor Name:iOMEDICO AG | |||||||||||||
Full Title: Capecitabine and bevacizumab ± vinorelbine as 1st line treatment in HER2/neu-negative metastatic or locally advanced inoperable breast cancer patients | |||||||||||||
Medical condition: HER-2/neu negative metastatic or locally advanced inoperable breast cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000665-35 | Sponsor Protocol Number: PM0259CA220B0 | Start Date*: 2004-09-08 |
Sponsor Name:Pierre Fabre Medicament | ||
Full Title: Phase II study of oral vinorelbine in combination with capecitabine in metastatic breast cancer patients previously treated with anthracyclines and taxanes | ||
Medical condition: Treatment in metastatic breast cancer women previously treated with anthracyclines and taxanes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
