Actively Recruiting

Phase 2
Age: 18Years +
MALE
NCT05762536

Docetaxel or Cabazitaxel With or Without Darolutamide in mCRPC

Led by Erasmus Medical Center · Updated on 2024-06-27

245

Participants Needed

1

Research Sites

230 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Taxane efficacy in metastatic prostate cancer is modest due to resistance development. Several clinical phase III studies in metastatic castration-naïve prostate cancer (mCNPC) patients have shown that adding an androgen receptor signalling inhibitor (ARSi) to patients receiving a taxane and androgen deprivation therapy (ADT) improves survival endpoints. Adding ARSi darolutamide to docetaxel+ADT in mCNPC patients resulted in a robust OS benefit (HR 0.68). Importantly, the combination of a taxane and darolutamide is not prone to a drug-drug interaction, while there is a detrimental CYP3A4 inducing effect in the case of enzalutamide, resulting in a significant and clinically relevant reduction of cabazitaxel plasma concentrations. The investigators have previously reported preclinical data showing that addition of an androgen receptor signaling inhibitor (ARSi) improves cabazitaxel efficacy, even in metastatic castration-resistant prostate cancer (mCRPC). As treatment options for mCRPC) patients are scarce and patients often develop drug resistance relatively early, a new treatment regimen for this population to delay drug resistance is highly desired. The investigators propose a randomized phase II trial to investigate the efficacy of docetaxel or cabazitaxel plus darolutamide compared to docetaxel or cabazitaxel monotherapy in men with metastatic CRPC, who have progressed on an ARSI.

CONDITIONS

Official Title

Docetaxel or Cabazitaxel With or Without Darolutamide in mCRPC

Who Can Participate

Age: 18Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Confirmed diagnosis of progressive metastatic castration-resistant prostate cancer with castrate testosterone levels below 0.5 ng/mL
  • Disease progression after at least one androgen receptor signaling inhibitor treatment (abiraterone, apalutamide, darolutamide, or enzalutamide)
  • Previous use of docetaxel in metastatic castration-naive setting allowed if receiving cabazitaxel in this study
  • WHO performance status of 2 or less
  • Ability and willingness to sign informed consent before screening
  • Adequate blood, kidney, and liver function and chemistry
Not Eligible

You will not qualify if you...

  • Unable or unwilling to take oral medications
  • Allergy or hypersensitivity to taxane chemotherapy drugs
  • Serious or unstable medical illnesses such as HIV, hepatitis, Varicella zoster or herpes zoster infection, organ transplant, kidney failure, severe liver disease, or cardiac and respiratory diseases
  • Symptomatic peripheral neuropathy grade 2 or higher
  • Prior rechallenge with docetaxel

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Erasmus MC Cancer Institute

Rotterdam, Netherlands, 3015GD

Actively Recruiting

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Research Team

T

Tanja van Dijk

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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