CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 11,992 enrolled
Drug / intervention
Celecoxib +9 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00268476
NCT00268476Phase 3Active

STAMPEDE: Systemic Therapy in Advancing or Metastatic Prostate Cancer: Evaluation of Drug Efficacy: A Multi-Stage Multi-Arm Randomised Controlled Trial

Medical Research Council·interventional·Posted Dec 22, 2005·Updated Apr 18, 2023

In Brief

A Phase 3 clinical trial evaluating Celecoxib, Docetaxel, and 8 other interventions for Prostate Cancer. Active but no longer recruiting, targeting 11,992 participants across 120 sites in 2 countries.

Detailed Summary

The overall aim of this trial, which is called STAMPEDE, is to assess novel approaches for the treatment of men with prostate cancer who are starting long-term ADT for the first time, termed hormone-naïve prostate cancer. This trial aims to see if we can improve the way in which prostate cancer is currently managed, either by adding new treatments to the standard approach or by modifying the type of hormone therapy aiming to improve quality-of-life by reducing the side effects of treatment. Each new treatment approach is compared against a control arm receiving the current standard treatments. We aim to identify treatment strategies that enable men to live longer, or as long but with an improved quality-of-life, as well as offering value for money for the health service. Since opening to accrual in Oct-2005, the trial has tested many ways of treating prostate cancer and some results are now already known. More than 10,000 men will join the trial with answers becoming available throughout the trial. New patients joining the trial from Protocol version 17.0 onwards (activated in December 2018) may be eligible to join one of two treatment comparisons, metformin (treatment group K; the "metformin comparison") and transdermal oestradiol (treatment group L; the "transdermal oestradiol comparison"). A computer program will be used to allocate which treatment each participant receives, using a chance process. Summary of the research arms in STAMPEDE trial platform Summary of research treatment groups currently open to recruitment (June 2017) 1. Metformin (Arm K): This anti-diabetic medication is proposed to have both anti-cancer effects and may help prevent the adverse metabolic effects of long-term ADT. STAMPEDE will investigate whether adding metformin to the current standard-of-care for non-diabetic men can improve all-cause survival. 2. Transdermal oestradiol (Arm L): This is an alternative form of hormone treatment which has been shown to suppress testosterone as effectively as standard ADT and avoid some of the side-effects. It may also help to avoid the adverse metabolic effects and fatigue and therefore improve overall quality of life compared with standard forms of ADT. STAMPEDE will investigate whether transdermal oestradiol can treat the cancer as well as current standard forms of ADT. 3. Control group (Arm A): Patients allocated to this group receive the current standard-of-care ADT +/- RT +/- docetaxel.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsProstate Cancer
CountriesSwitzerland, United Kingdom
Collaborators--

Timeline

Phase 3Active
200520062007200820092010201120122013201420152016201720182019202020212022202320242025202620272028202920302031
First PostedDec 22, 2005
Enrollment StartJul 8, 2005
Primary CompletionMar 1, 2026
Study CompletionDec 1, 2030
TodayJul 2, 2026
Enrollment to primary: 20.6 yearsPosted 20.5 years ago

Interventions

Celecoxibdrug

Docetaxeldrug

Prednisolonedrug

ADTdrug

Zoledronic Aciddrug

Abirateronedrug

Radiotherapy to the prostateradiation

Enzalutamidedrug

Metformindrug

Transdermal Oestradioldrug