Systemic Therapy in Advancing or Metastatic Prostate Cancer: Evaluation of Drug Efficacy

Study acronym: STAMPEDE
StatusActive, Not Recruiting
PhasePhase 2/3
Started

Record status This record was last updated April 18, 2023 (before its estimated March 2026 completion). Its status may not reflect the trial's current state.

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Record History

The 50 most recent of 64 record versions are listed below. See every version on ClinicalTrials.gov ↗

  1. Notable Primary completion date: Sep 2024 to Mar 2026
    • Trial status: Recruiting to Active, Not Recruiting
    • Enrollment target: estimated 12200 to confirmed 11992
    • Site details revised at 120 of 120 sites
    v64
  2. Minor Secondary endpoints: details revised at 1 of 13 entriesv63
  3. Minor Eligibility criteria expanded, about 119 wordsv62
  4. Minor Study completion date: Sep 2024 to Dec 2030
    • Publications: 32 to 33
    v61
  5. Minor Site details revised at 4 of 120 sitesv60
Show 45 earlier versionsHide 45 earlier versions
  1. Minor Enrollment target: 11200 to 12200
    • Eligibility criteria shortened, about 150 words
    • Publications: 28 to 32
    v59
  2. Minor Secondary endpoints revised (13)v58
  3. Minor Secondary endpoints revised (13)v57
  4. Re-verified, no change to tracked fieldsv56
  5. Minor Enrollment target: 8100 to 11200v55 Show 6 more changesShow less
    • Start date: Sep 2005 to Jul 8, 2005
    • Interventions: ADT (Drug), Abiraterone (Drug), Celecoxib (Drug), Docetaxel (Drug), Enzalutamide (Drug), Metformin (Drug), Orchiectomy (Procedure)… to ADT (Drug), Abiraterone (Drug), Celecoxib (Drug), Docetaxel (Drug), Enzalutamide (Drug), Metformin (Drug), Prednisolone (Drug)…
    • Eligibility criteria expanded, about 208 words
    • Secondary endpoints: details revised at 13 of 13 entries
    • Study sites revised (120)
    • Study title shortened, about 7 words
  6. Notable Primary completion date: Sep 2017 to Sep 2024v54 Show 7 more changesShow less
    • Study completion date: Sep 2024
    • Interventions: ADT (Drug), Radiotherapy to the prostate (Radiation), abiraterone (Drug), celecoxib (Drug), docetaxel (Drug), enzalutamide (Drug)… to ADT (Drug), Abiraterone (Drug), Celecoxib (Drug), Docetaxel (Drug), Enzalutamide (Drug), Metformin (Drug), Orchiectomy (Procedure)…
    • Eligibility criteria expanded, about 47 words
    • Secondary endpoints: 5 to 13
    • Study description shortened, about 47 words
    • Site details revised at 4 of 120 sites
    • Study arms: 9 to 11
  7. Notable Enrollment target: 5000 to 8100v53 Show 6 more changesShow less
    • Study sites: 116 to 120
    • Interventions: Radiotherapy to the prostate (Radiation), abiraterone (Drug), celecoxib (Drug), docetaxel (Drug), orchiectomy (Procedure), prednisolone… to ADT (Drug), Radiotherapy to the prostate (Radiation), abiraterone (Drug), celecoxib (Drug), docetaxel (Drug), enzalutamide (Drug)…
    • Eligibility criteria expanded, about 70 words
    • Study description expanded, about 67 words
    • Publications: 27 to 28
    • Study arms: 8 to 9
  8. Notable Primary completion date: Sep 2015 to Sep 2017v52 Show 7 more changesShow less
    • Enrollment target: 4000 to 5000
    • Study sites: 107 to 116
    • Interventions: abiraterone (Drug), celecoxib (Drug), docetaxel (Drug), orchiectomy (Procedure), prednisolone (Drug), releasing hormone agonist therapy… to Radiotherapy to the prostate (Radiation), abiraterone (Drug), celecoxib (Drug), docetaxel (Drug), orchiectomy (Procedure), prednisolone…
    • Eligibility criteria expanded, about 59 words
    • Study description expanded, about 88 words
    • Publications: details revised at 2 of 27 entries
    • Study arms: 7 to 8
  9. Notable Lead sponsor: Dominic Hague to Medical Research Councilv51
  10. Notable Lead sponsor: Medical Research Council to Dominic Haguev50 Show 10 more changesShow less
    • Primary endpoint revised
    • Enrollment target: 3300 to 4000
    • Study sites: 95 to 107
    • Primary completion date: Sep 2015
    • Interventions: celecoxib (Drug), docetaxel (Drug), orchiectomy (Procedure), prednisolone (Drug), releasing hormone agonist therapy (Drug), zoledronic acid… to abiraterone (Drug), celecoxib (Drug), docetaxel (Drug), orchiectomy (Procedure), prednisolone (Drug), releasing hormone agonist therapy…
    • Eligibility criteria expanded, about 137 words
    • Secondary endpoints reordered
    • Study description expanded, about 65 words
    • Study arms: 0 to 7
    • Study title shortened, about 2 words
  11. Minor Study sites revised (95)v49
  12. Minor Site details revised at 1 of 95 sitesv48
  13. Minor Study sites: 41 to 95v47
  14. Minor Publications: 26 to 27v46
  15. Minor Publications: details revised at 1 of 26 entriesv45
  16. Minor Study sites revised (41)v44
  17. Minor Site contacts updated at 1 of 41 sitesv43
  18. Minor Interventions: celecoxib (Drug), docetaxel (Drug), orchiectomy (Procedure), prednisolone (Drug), releasing hormone agonist therapy (Procedure), zoledronic… to celecoxib (Drug), docetaxel (Drug), orchiectomy (Procedure), prednisolone (Drug), releasing hormone agonist therapy (Drug), zoledronic acid…v42
  19. Minor Study sites revised (41)v41
  20. Re-verified, no change to tracked fieldsv40
  21. Minor Interventions: antiangiogenesis therapy (Procedure), bone metastases treatment (Procedure), celecoxib (Drug), chemotherapy (Procedure), docetaxel (Drug)… to celecoxib (Drug), docetaxel (Drug), orchiectomy (Procedure), prednisolone (Drug), releasing hormone agonist therapy (Procedure), zoledronic…v39
  22. Minor Study sites: 35 to 41v38
  23. Re-verified, no change to tracked fieldsv37
  24. Minor Study sites revised (35)v36
  25. Notable Lead sponsor: University Hospital Birmingham to Medical Research Councilv35
  26. Minor Study sites revised (35)v34
  27. Minor Study sites revised (35)v33
  28. Re-verified, no change to tracked fieldsv32
  29. Minor Site contacts updated at 1 of 35 sitesv31
  30. Minor Study sites revised (35)v30
  31. Minor Site details revised at 1 of 35 sitesv29
  32. Minor Interventions: antiangiogenesis therapy (Procedure), bone metastases prevention (Procedure), celecoxib (Drug), chemotherapy (Procedure), docetaxel (Drug)… to antiangiogenesis therapy (Procedure), bone metastases treatment (Procedure), celecoxib (Drug), chemotherapy (Procedure), docetaxel (Drug)…v28
  33. Minor Study sites revised (35)v27
  34. Minor Interventions: Intervention/procedure (Procedure), ablation therapy (Procedure), ablative endocrine surgery (Procedure), anti-cytokine therapy… to antiangiogenesis therapy (Procedure), bone metastases prevention (Procedure), celecoxib (Drug), chemotherapy (Procedure), docetaxel (Drug)…v26
  35. Minor Interventions: ablation therapy (Procedure), ablative endocrine surgery (Procedure), anti-cytokine therapy (Procedure), antiangiogenesis therapy… to Intervention/procedure (Procedure), ablation therapy (Procedure), ablative endocrine surgery (Procedure), anti-cytokine therapy…v25
  36. Minor Study sites: 23 to 35v24
  37. Minor Site contacts updated at 1 of 23 sitesv23
  38. Minor Site contacts updated at 2 of 23 sitesv22
  39. Minor Study sites revised (23)v21
  40. Minor Interventions: ablative endocrine surgery (Procedure), anti-cytokine therapy (Procedure), antiangiogenesis therapy (Procedure), biological therapy… to ablation therapy (Procedure), ablative endocrine surgery (Procedure), anti-cytokine therapy (Procedure), antiangiogenesis therapy…v20
  41. Minor Site contacts updated at 1 of 23 sitesv19
  42. Minor Study sites: 15 to 23v18
  43. Minor Interventions: ablative endocrine surgery (Procedure), anti-cytokine therapy (Procedure), antiangiogenesis therapy (Procedure), biological therapy… to ablative endocrine surgery (Procedure), anti-cytokine therapy (Procedure), antiangiogenesis therapy (Procedure), biological therapy…v17
  44. Re-verified, no change to tracked fieldsv16
  45. Minor Study description expanded, about 10 wordsv15
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT00268476
Lead Sponsor Medical Research Council
Conditions
(from sponsor)
Prostate Cancer
Related terms Prostatic Neoplasms
Enrollment 11,992 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov