- Trials with a EudraCT protocol (151)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
151 result(s) found for: Gemcitabine and Carboplatin.
Displaying page 1 of 8.
| EudraCT Number: 2004-003868-30 | Sponsor Protocol Number: LU3005 | Start Date*: 2007-07-04 |
| Sponsor Name:University of Birmingham [...] | ||
| Full Title: BTOG2: A British Thoracic Oncology Group phase III trial of gemcitabine plus cisplatin at 80 mg/m2 versus gemcitabine plus cisplatin at 50 mg/m2 versus gemcitabine plus carboplatin AUC 6 in stage I... | ||
| Medical condition: Non-small cell lung cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IE (Completed) GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-005197-40 | Sponsor Protocol Number: I1D-MC-JIAE | Start Date*: 2012-07-20 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Phase 1b/2 Study of LY2228820, a p38MAPK Inhibitor, plus Gemcitabine and Carboplatin versus Gemcitabine and Carboplatin for Women with Platinum-Sensit... | |||||||||||||
| Medical condition: Epithelial ovarian cancer, fallopian tube cancer, and primary peritoneal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-016050-41 | Sponsor Protocol Number: E7080-701 | Start Date*: 2010-07-29 | |||||||||||
| Sponsor Name:Eisai Inc. | |||||||||||||
| Full Title: An Open-Label, Multicenter, Randomized, Phase Ib/II Study of E7080 in Combination with Carboplatin + Gemcitabine versus Carboplatin + Gemcitabine Alone as Second Line Therapy in Patients with Plati... | |||||||||||||
| Medical condition: Platinum-Sensitive Recurrent Ovarian Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-000744-17 | Sponsor Protocol Number: LONG 05-05 | Start Date*: 2006-03-22 |
| Sponsor Name:University Hospital Ghent | ||
| Full Title: A randomised phase II study evaluating two schedules of the 21-day regimen of Gemcitabine and Carboplatin in advanced NSCLC | ||
| Medical condition: Non-small cell lung cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-003040-20 | Sponsor Protocol Number: MX39795 | Start Date*: 2018-06-20 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A phase II, randomized, active-controlled, multi-center study comparing the efficacy and safety of targeted therapy or cancer immunotherapy guided by genomic profiling versus platinum-based chemoth... | |||||||||||||
| Medical condition: Cancer of Unknown Primary Site | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) AT (Completed) EE (Completed) IE (Completed) DE (Completed) CZ (Completed) FI (Completed) LV (Completed) HU (Completed) PL (Completed) FR (Completed) ES (Ongoing) BG (Completed) PT (Completed) HR (Completed) NO (Completed) NL (Completed) DK (Completed) CY (Prematurely Ended) IT (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000199-25 | Sponsor Protocol Number: 009436 | Start Date*: 2014-04-22 |
| Sponsor Name:Queen Mary, University of London | ||
| Full Title: A Phase II, randomised, open-label study of Gemcitabine/Carboplatin first-line chemotherapy in combination with or without the antisense oligonucleotide Apatorsen (OGX-427) in advanced squamous cel... | ||
| Medical condition: Advanced squamous cell lung cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-000126-31 | Sponsor Protocol Number: 1401 | Start Date*: 2006-06-24 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: A phase II trial of carboplatin and paclitaxel compared with carboplatin or gemcitabine paclitaxel "induction" followed by carboplatin/paclitaxel/gemcitabine in patients with suboptimally resected ... | |||||||||||||
| Medical condition: Epithelial ovarian carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000171-24 | Sponsor Protocol Number: GCTSK004 | Start Date*: 2016-07-12 |
| Sponsor Name:Národný onkologický ústav | ||
| Full Title: Phase II study of gemcitabine, carboplatin and VELIPARIB (ABT-888) in refractory testicular germ cell cancer. | ||
| Medical condition: Refractory histologically confirmed extracranial primary germ cell cancer, seminoma, or nonseminoma germ cell tumours | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: SK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-000722-69 | Sponsor Protocol Number: GEICO-0104 | Start Date*: 2004-11-25 | |||||||||||
| Sponsor Name:Grupo Español de Investigación en Cáncer de Ovario (GEICO) | |||||||||||||
| Full Title: A PHASE II, RANDOMIZED STUDY OF CARBOPLATIN-GEMCITABINE PLUS CARBOPLATIN-PACLITAXEL VERSUS CARBOPLATIN-PACLITAXEL IN PLATINUM-SENSITIVE PATIENTS WITH RECURRENT OVARIAN CARCINOMA, PRIMARY PERITONEAL... | |||||||||||||
| Medical condition: Ovarian Carcinoma (MedDRA 6.1, PT:10033128), Primary Peritoneal Carcinoma (MedDRA 6.1, PT:10052171) and Fallopian Tube Cancer (MedDRA 6.1, PT:10016180), | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004260-36 | Sponsor Protocol Number: MS100070_0160 | Start Date*: 2018-03-12 | |||||||||||
| Sponsor Name:Associació Per a la Recerca Oncològica (APRO) | |||||||||||||
| Full Title: Phase II multicentre, randomized, open-label study to evaluate the safety and efficacy of avelumab with gemcitabine/carboplatin versus gemcitabine/carboplatin alone in patients with unresectable or... | |||||||||||||
| Medical condition: Unresectable or metastatic urothelial carcinoma in patients without prior systemic therapy and who are ineligible to receive cisplatin-based therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000886-30 | Sponsor Protocol Number: D6010C00004 | Start Date*: 2015-07-29 |
| Sponsor Name:AstraZeneca AB | ||
| Full Title: A Multicentre Phase II Study of AZD1775 plus Chemotherapy in Patients with Platinum-Resistant Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer. | ||
| Medical condition: Platinum-Resistant Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (Completed) NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-005018-47 | Sponsor Protocol Number: 008-IRCC-10IIS-14 | Start Date*: 2015-04-08 | |||||||||||
| Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCCS | |||||||||||||
| Full Title: A PHASE II, RANDOMIZED, MULTICENTER STUDY TO ASSESS THE EFFICACY OF NAB-PACLITAXEL-BASED DOUBLET AS FIRST LINE THERAPY IN PATIENTS WITH CANCER OF UNKNOWN PRIMARY (CUP): the AGNOSTOS trial | |||||||||||||
| Medical condition: Cancers of Unknown Primary (CUP) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-000113-20 | Sponsor Protocol Number: ABI-007-MBC-001 | Start Date*: 2013-07-23 | ||||||||||||||||
| Sponsor Name:Abraxis BioScience, LLC, a wholly-owned subsidiary of Celgene Corporation | ||||||||||||||||||
| Full Title: A PHASE 2/3, MULTI-CENTER, OPEN-LABEL, RANDOMIZED STUDY OF WEEKLY nab®-PACLITAXEL IN COMBINATION WITH GEMCITABINE OR CARBOPLATIN, COMPARED TO GEMCITABINE/CARBOPLATIN, AS FIRST LINE TREATMENT IN SUB... | ||||||||||||||||||
| Medical condition: ER, PgR, and HER2 negative (triple negative) metastatic breast cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: AT (Prematurely Ended) ES (Completed) DE (Prematurely Ended) GB (Prematurely Ended) IT (Completed) PT (Prematurely Ended) GR (Prematurely Ended) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-000179-29 | Sponsor Protocol Number: CMCS110Z2201 | Start Date*: 2015-04-14 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A randomized phase II study of MCS110 combined with carboplatin and gemcitabine in advanced Triple Negative Breast Cancer (TNBC) | |||||||||||||
| Medical condition: Advanced Triple Negative Breast Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) AT (Prematurely Ended) ES (Completed) BE (Prematurely Ended) FR (Prematurely Ended) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003881-14 | Sponsor Protocol Number: CA209-901 | Start Date*: 2017-06-12 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Phase 3, Open-label, Randomized Study of Nivolumab Combined with Ipilimumab, or with Standard of Care Chemotherapy, versus Standard of Care Chemotherapy in Participants with Previously Untreated ... | |||||||||||||
| Medical condition: Untreated Unresectable or Metastatic Urothelial Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) SE (Completed) FI (Completed) FR (Trial now transitioned) GR (Trial now transitioned) NO (Trial now transitioned) CZ (Trial now transitioned) DK (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-010140-33 | Sponsor Protocol Number: SPON672-09 | Start Date*: 2009-11-13 |
| Sponsor Name:Cardiff University | ||
| Full Title: A randomised phase II Trial of carboplatin and gemcitabine +/- vandetanib in first line treatment Of advanced Urothelial cell Cancer in patients who are not suitable to receive cisplatin | ||
| Medical condition: Transitional cell carcinoma of urothelium (upper or lower urinary tract). Cancers with other pathologies are permitted, provided that the dominant morphology is transitional cell carcinoma. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-004466-26 | Sponsor Protocol Number: G1T28-04 | Start Date*: 2017-07-10 | |||||||||||
| Sponsor Name:G1 Therapeutics | |||||||||||||
| Full Title: Phase 2 Study of the Safety, Efficacy, and Pharmacokinetics of G1T28 in Patients with Metastatic Triple Negative Breast Cancer Receiving Gemcitabine and Carboplatin Chemotherapy | |||||||||||||
| Medical condition: Locally recurrent or metastatic Triple Negative Breast Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) SI (Completed) HR (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001892-35 | Sponsor Protocol Number: MK-7339-009 | Start Date*: 2019-12-10 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co.,Inc | |||||||||||||
| Full Title: An Open-label, Randomized, Phase 2/3 Study of Olaparib Plus Pembrolizumab Versus Chemotherapy Plus Pembrolizumab After Induction of Clinical Benefit With First-line Chemotherapy Plus Pembrolizumab ... | |||||||||||||
| Medical condition: Locally Recurrent Inoperable or Metastatic Triple Negative Breast Cancer (TNBC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) PL (Trial now transitioned) HU (Trial now transitioned) IE (Trial now transitioned) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-004170-15 | Sponsor Protocol Number: UCL/12/2015 | Start Date*: 2016-11-17 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: A multicentre, randomised trial comparing combination gemcitabine/carboplatin and hydroxychloroquine versus carboplatin/etoposide therapy alone in small cell lung cancer (SCLC) | |||||||||||||
| Medical condition: Small cell lung cancer | |||||||||||||
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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: 2005-001577-97 | Sponsor Protocol Number: The PAGe study | Start Date*: 2005-11-09 |
| Sponsor Name:Gunnar Hillerdal | ||
| Full Title: Treatment of locally advanced or metastatic non-small cell lung cancer with Pemetrexed (Alimta) and Gemcitabine or Gemcitabine and Carboplatin: The PAGe study. | ||
| Medical condition: Icke småcellig lungcancer i stadium IIIB eller IV. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
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