Cabazitaxel (XRP6258)
DrugPharmaceutical form: solution Route of administration: intravenous
NCT Number: NCT01649635
Primary Objective:
- To assess effectiveness of prophylactic treatment of hematological complications (grade ≥ 3 neutropenia) resulting from cabazitaxel treatment for 21 days after treatment initiation.
Secondary Objectives:
* PSA response rate; * Descriptive assessment of CTC (circulating Tumor Cells); * Rates of grade ≥ 3 neutropenia and febrile neutropenia and grade ≥3 diarrhea over the treatment period; * Description of the Health Quality of Life of the patients; * Incidence of adverse events.
Looking for future studies?
Notify Me18 year and older
Male
Interventional
Phase 4
Investigational Site Number 007, Centro, Brazil
Screening: 15 days Treatment: until disease progression Post-treatment Follow-up: 12 months
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Pharmaceutical form: solution Route of administration: intravenous
Pharmaceutical form: tablet Route of administration: oral
Pharmaceutical form: tablet Route of administration: oral
Pharmaceutical form: solution Route of administration: subcutaneous
Time frame: 21 days
Time frame: up to 24 months (every 21 days)
Time frame: up to 24 months (every 21 days)
Time frame: up to 24 months (every 21 days)
Time frame: up to 24 months (every 21 days)
Time frame: Day 42, Day 84, Day 126 and End of Treatment
Time frame: up to 24 months (every 21 days)
Time frame: up to 24 months (every 21 days)
Sanofi
Industry
A Phase IV, Multicenter, National, Non-comparative, Open-label Study of Cabazitaxel, Combined With Prednisone and Prophylaxis of Neutropenia Complications in the Second-line Treatment of Patients With Metastatic Castration-resistant Prostate Cancer and After Failure of Docetaxel-based Chemotherapy. Descriptive Assessment of the Circulating Tumor Cells in This Context.
Acronym: PROSPECTA
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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