Impact of Atorvastatin on Prostate Cancer Progression During ADT

NCT04026230 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 400

Last updated 2022-10-21

No results posted yet for this study

Summary

This randomized double-blind placebo-controlled trial tests whether intervention with atorvastatin delays development of castration resistance compared to placebo during androgen deprivation therapy (ADT) for prostate cancer.

Conditions

Interventions

DRUG

Atorvastatin 80mg

Capsules including 80 mg of atorvastatin

DRUG

Placebo oral capsule

Similar capsules as in the atorvastatin arm, but without the active ingredient

Sponsors & Collaborators

  • Turku University Hospital

    collaborator OTHER_GOV
  • Central Finland Hospital District

    collaborator OTHER
  • Tartu University Hospital

    collaborator OTHER
  • University of Aarhus

    collaborator OTHER
  • Fimlab laboratories

    collaborator UNKNOWN
  • Helsinki University Central Hospital

    collaborator OTHER
  • Kuopio University Hospital

    collaborator OTHER
  • Oulu University Hospital

    collaborator OTHER
  • Seinajoki Central Hospital

    collaborator OTHER
  • The Hospital of Vestfold

    collaborator OTHER
  • Telemark Hospital Trust

    collaborator UNKNOWN
  • Tampere University Hospital

    lead OTHER

Principal Investigators

  • Teemu Murtola, MD, PhD · Tampere University Hospital

  • Otto Ettala, MD, PhD · Turku University Hospital

  • Heikki Seikkula · Central Finland Central Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-15
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • Denmark
  • Estonia
  • Finland
  • Norway

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04026230 on ClinicalTrials.gov