Overview

ModraDoc006/r in Metastatic Castration-resistant Prostate Cancer

Status:
Completed
Trial end date:
2019-09-05
Target enrollment:
Participant gender:
Summary
This is a safety, feasibility and pharmacokinetic study to confirm that the recommended safe dose and schedule of ModraDoc006/r (oral docetaxel with ritonavir) as determined in a previous phase I study is also safe and feasible in the target population of patients with CRPC.
Phase:
Phase 1
Details
Lead Sponsor:
Modra Pharmaceuticals
Collaborator:
The Netherlands Cancer Institute
Treatments:
Docetaxel