drugset / Trial / NCT02441894

Combination of Cabazitaxel With Prednisolone With Primary Prophylaxis With PEG-G-CSF in Treatment of Patients With Prostate Cancer

NCT02441894

Phase 4 Completed 21 enrolled Sanofi
NaSingle-groupOpen-labelTreatment

Summary

Primary Objective: To assess the tolerability of cabazitaxel 25 mg per body surface area (m\^2) with primary prophylactic polyethylene glycol-granulocyte-colony stimulating factor (PEG-G-CSF) in terms of the incidence rate of febrile neutropenia (FN) (defined: absolute neutrophil count \[ANC\] \<1000 per volume \[mm\^3\] and a single temperature of \>38.3 degree or a sustained temperature of ≥38 degree Celsius for more than one hour) during Cycle 1. Secondary Objective: To assess overall rate of FN and grade ≥3 neutropenia and diarrhea; frequencies of dose delay due to adverse events (AEs); dose reduction due to AEs; relative dose intensity; incidences of FN-related hospitalization and use of intravenous (IV) anti-infectives; tolerability according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) v4.0; prostate specific antigen (PSA) response (50% decrease); tumor response according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 if available.

Timeline

Start
2015-04
Primary completion
2016-02
Completion
2016-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Cabazitaxel Other / unclassified 25 mg/m2 Intravenous
Subject Pegfilgrastim Protein / enzyme biologic 3.6 mg Subcutaneous
Background Dexamethasone Small molecule Oral
Background Dexchlorpheniramine Unknown Oral
Background Diphenhydramine Unknown Oral
Background Granisetron Other / unclassified Oral
Background Metoclopramide Small molecule Oral
Background Ondansetron Other / unclassified Oral
Background Prednisolone Other / unclassified 10 mg Oral
Background Ranitidine Unknown Oral

Indications