trastuzumab
BiologicalBottles of 150 mg; Charging dose: 8mg/kg then 6mg/kg every 21 days given IV
Other names: anti-c-erB-2, Herceptin, MOAB HER2
NCT Number: NCT01828736
A multicenter, randomized, Phase 2 trial to study the effectiveness and feasibility of association of trastuzumab with combination chemotherapy in advanced or metastatic bladder cancer patients. Combining monoclonal antibody therapy with combination chemotherapy may improve treatment efficacy on tumours overexpressed HER 2.
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Notify Me18 year–80 year
All sexes
Interventional
Phase 2
Cliniques saint Luc - Université Catholique de Louvain, Brussels, Belgium
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Hematological criteria: - Neutrophils> 1.5 x 109 / L, - Chips> 100 x 109 / L - Hemoglobin> 10 g / dL, Liver function: - Alkaline phosphatase (unless bone metastases) <2 x N - Total bilirubin <1.5 x N - transaminases (AST, ALT) <1.5 x N, renal Constants: - Creatinine clearance > 30 ml / min (Cockcroft and Gault, cf. Annex XV protocol)
Exclusion criteria
Bottles of 150 mg; Charging dose: 8mg/kg then 6mg/kg every 21 days given IV
Other names: anti-c-erB-2, Herceptin, MOAB HER2
Given IV, 1000 mg/m² BSA on Day 1 and Day 8 every 21 days
Other names: dFdC, difluorodeoxycytidine hydrochloride, Gemzar, gemcitabin hydrochloride
Given IV: AUC 5 on Day 1 every 21 days
Other names: Carboplat, CBDCA, JM-8, Paraplat, Paraplatin
Given IV, 70 mg/m² BSA on day 1 every 21 days
Other names: cis-Diamminedichloroplatinum(II), Platinum Diamminodichloride, Diamminodichloride, Platinum, cis-Platinum, cis Platinum, Dichlorodiammineplatinum, cis-Diamminedichloroplatinum, cis Diamminedichloroplatinum, cis-Dichlorodiammineplatinum(II), Platinol, Platidiam, Platino, NSC-119875, Biocisplatinum
Time frame: Participants will be followed from radomization until progression or death, up to 3 years
Time frame: Objective Response Rate will be assessed during treatment period, every 3 cycles, up to 7 months
Time frame: Participants will be followed all along the study period, an expected average of 3 years
Toxicity will be classify according to NCI-CTC criteria Version 2.0. Cardiac toxicity will be assessed according to the NYHA (New York Heart Association) criteria.
Time frame: Quality of Life will be assessed during the study period, every 3 cycles (Arm A patients) or every 3 months (Arm B patients), up to 3 years
Quality of Life will be assessed according to the EORTC QLQ-C30 Version 3 questionnaire
Time frame: Participants will be followed from randomization until death or lost of follow-up, up to 3 years
Association Pour La Recherche des Thérapeutiques Innovantes en Cancérologie
Other
Multicenter Randomized Phase 2 Trial of Gemcitabine - Platinum With or Without Trastuzumab in Advanced or Metastatic Urothelial Carcinoma With HER2 Overexpression
Acronym: CVH-CT02
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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