AzTrials
AzTrials

Prostate CancerPhase 4PLATONCT01995513

Safety Study of Continued Enzalutamide Treatment In Prostate Cancer Patients

A Phase 4 study testing Enzalutamide, Abiraterone and Prednisone in people with Prostate Cancer, run by Pfizer at 95 sites in 11 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The purpose of this study is to determine if continued treatment with Enzalutamide is effective in patients with metastatic prostate cancer. Read more about this study

Who is it for?
Ages 18 years and older, men only
Conditions the study is for
Prostate Cancer
What is being tested?
Enzalutamide, Abiraterone and Prednisone
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
509 participants
Where
95 sitesin 11 countries
Study dates
22 Oct 2013to 31 Aug 2022
Phase
Phase 4
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Men only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Men with metastatic castration-resistant prostate cancer
  • Progressive disease on androgen deprivation therapy
  • Patients must agree to continue androgen deprivation therapy with a GnRH agonist/antagonist throughout the study or have had a prior bilateral orchiectomy
  • ECOG performance score ≤ 1
  • Estimated life expectancy of ≥ 12 months

Who cannot join

  • Prior cytotoxic chemotherapy, aminoglutethimide, ketoconazole, abiraterone, or enzalutamide for the treatment of prostate cancer
  • Prior participation in a clinical trial of an investigational agent that inhibits the androgen receptor or androgen synthesis (unless the treatment was placebo)
  • History of brain metastasis, active leptomeningeal disease or seizure
  • Severe cardiovascular or hepatic disease
  • Pituitary or adrenal dysfunction

Trial locations and contacts

95 sites in 11 countries.

95 sites in 11 countries

Australia35 sites
  • Border Medical Oncology Research Unit

    Albury, New South Wales, 2640

  • Ramsay Health Care Australia Pty Ltd

    Albury, New South Wales, 2640

  • Regional Imaging Border

    Albury, New South Wales, 2640

  • Terry White Chemist

    Albury, New South Wales, 2640

  • Icon Cancer Care Wesley

    Auchenflower, Queensland, 4066

  • River City Pharmacy - APHS

    Auchenflower, Queensland, 4066

  • Moorabbin Radiology

    Bentleigh East, Victoria, 3165

  • Box Hill Hospital

    Box Hill, Victoria, 3128

  • Icon Cancer Care Chermside

    Chermside, Queensland, 4032

  • Monash Medical Centre

    Clayton, Victoria, 3168

  • Concord Cancer Centre, Medical Oncology Department

    Concord, New South Wales, 2139

  • Concord Hospital Clinical Trials Pharmacy

    Concord, New South Wales, 2139

  • Gold Coast Radiology PTY LTD

    Hope Island, Queensland, 4212

  • Adelaide Cancer Centre

    Kurralta Park, South Australia, 5037

  • Ashford Cancer Centre Research

    Kurralta Park, South Australia, 5037

  • Cancer Care SA Pty Ltd

    Kurralta Park, South Australia, 5037

  • Tenpharm Pty Ltd trading as EPIC Pharmacy Tennyson

    Kurralta Park, South Australia, 5037

  • Epic Pharmacy Lismore

    Lismore, New South Wales, 2480

  • Cabrini Health - Cabrini Hospital

    Malvern, Victoria, 3144

  • Macquarie University Hospital Pharmacy

    North Ryde, New South Wales, 2109

  • Macquarie University

    North Ryde, New South Wales, 2109

  • Epic Pharmacy Port Macquarie base hospital

    Port Macquarie, New South Wales, 2444

  • Port Macquarie Base Hospital,North Coast Cancer Institute

    Port Macquarie, New South Wales, 2444

  • Icon Cancer Care South Brisbane

    South Brisbane, Queensland, 4101

  • Icon Cancer Care

    South Brisbane, Queensland, 4101

  • North Shore Radiology and Nuclear Medicine

    St Leonards, New South Wales, 2065

  • Royal North Shore Hospital

    St Leonards, New South Wales, 2065

  • Sydney Adventist Hospital

    Sydney, New South Wales, 2076

  • South Coast Radiology

    Tugun, Queensland, 4224

  • Northern NSW Local Health District

    Tweed Heads, New South Wales, 2485

  • Queensland Diagnostic Imaging

    Tweed Heads, New South Wales, 2485

  • Sydney Adventist Hospital

    Wahroonga, New South Wales, 2076

  • Regional Imaging

    West Albury, New South Wales, 2640

  • Westmead Hospital

    Westmead, New South Wales, 2145

  • Border Medical Oncology

    Wodonga, Victoria, 3690

Other trials in Australia

Italy11 sites
  • Medicina Nucleare, Azienda Ospedaliera "Istituti Ospitalieri" di Cremona

    Cremona, 26100

  • Servizio di Radiologia, Azienda Ospedaliera "Istituti Ospitalieri" di Cremona

    Cremona, 26100

  • Struttura Complessa di Oncologia, Azienda Socio Sanitaria Territoriale di Cremona

    Cremona, 26100

  • U.O. Oncologia Medica, IRCCS Istituto Scientifico Romagnolo per lo Studio e la Cura

    Meldola, FC, 47014

  • Laboratorio Farmaci Antiblastici

    Meldola (FC), 47014

  • UO Radiologia

    Meldola (FC), 47014

  • SCDU Oncologia Medica II Pad, A.O.U. San Luigi Gonzaga

    Orbassano to, 10043

  • SCDU Radiodiagnostica, A.O.U. San Luigi Gonzaga

    Orbassano to, 10043

  • SS Medicina Nucleare, A.O.U. San Luigi Gonzaga

    Orbassano to, 10043

  • Azienda Ospedaliera S. Camillo Forlanini, UOC per il governo clinico in Oncologia Medica

    Roma, 00152

  • UOC Radiologia Piasta, Azienda Ospedaliera S. Camillo Forlanini

    Roma, 00512

Other trials in Italy

Slovakia10 sites
  • Fakultna nemocnica s poliklinikou F.D. Roosevelta

    Banská Bystrica, 975 17

  • Institut nuklearnej a molekularnej mediciny

    Banská Bystrica, 975 17

  • Fakultna nemocnica s poliklinikou F.D. Roosevelta

    Banská Bystrica, 97517

  • Bratislavske radiodiagnosticke centrum,a.s.

    Bratislava, 814 99

  • CUIMED, s.r.o., urologicka ambulancia

    Bratislava, 851 05

  • Univerzitna nemocnica martin

    Martin, 036 59

  • Jessenius-diagnosticke centrum, a.s.

    Nitra, 949 01

  • Uroexam, spol. s r.o., Urologicka ambulancia

    Nitra, 949 01

  • IZOTOPCENTRUM, s.r.o.

    Nitra, 950 01

  • GAMMALAB, spol.s r.o., Oddelenie nuklearnej mediciny

    Trnava, 917 01

Other trials in Slovakia

Spain9 sites
  • CO Badalona-Instituto Germans Trias i Pujol

    Badalona, Barcelona, 08916

  • ICO Badalona-Instituto Germans Trias i Pujol

    Badalona, Barcelona, 08916

  • ICO Badalona-Instituto Germans Trias i Pujol

    Badalona, Barcelon, 08916

  • Hospital del Mar

    Barcelona, 08003

  • Hospital Clinic de Barcelona

    Barcelona, 08036

  • Hospital Universitario Madrid Sanchinarro

    Madrid, 28050

  • ALTAHIA, Xarxa Assistencial Universitaria de Manresa

    Manresa, Barcelona, 08243

  • Hospital Universitario Son Espases

    Palma, Balearic Islands, 07120

  • Hospital Universitari Parc Tauli

    Sabadell, Barcelona, 08208

Other trials in Spain

United Kingdom7 sites
  • Velindre NHS Trust

    Cardiff, CF14 2TL

  • University College Hospitals NHS Trust

    London, NW1 2BU

  • The Royal Marsden NHS Foundation Trust

    London, SW3 6JJ

  • University College London Hospitals NHS Foundation Trust

    London, WC1E 6AG

  • East and North Hertfordshire NHS Trust

    Northwood, Middlesex, HA6 2RN

  • Oxford University Hospitals NHS Trust

    Oxford, OX3 7LE

  • The Royal Marsden NHS Foundation Trust

    Sutton, Surrey, SM2 5PT

Other trials in United Kingdom

United States6 sites
  • Beth Israel Deaconess Medical Center

    Boston, Massachusetts, 02115

  • Brigham & Women's Hospital

    Boston, Massachusetts, 02115

  • Beth Israel Deaconess Medical Center

    Boston, Massachusetts, 02215

  • Dana Farber Cancer Institute

    Boston, Massachusetts, 02215

  • eResearch Technology

    Philadelphia, Pennsylvania, 19103

  • Urology of Virginia, PLLC

    Virginia Beach, Virginia, 23462

Other trials in United States

Sweden6 sites
  • Urologmottagningen

    Gothenburg, 41345

  • Urologiska kliniken

    Malmö, 20502

  • Oriola

    Mölnlycke, 435 25

  • Apoteket AB Kliniska Provningar Molnlycke

    Mölnlycke, 435 33

  • Rontgenkliniken

    Örebro, 701 85

  • Urologmottagningen

    Örebro, 701 85

Other trials in Sweden

Denmark4 sites
  • Arhus Universitetshospital

    Arhus N, 8200

  • Rigshospitalet CPC 7521

    Copenhagen, Norrebro, 2200

  • Rigshospitalet

    Copenhagen, 2100

  • Frederiksberg Hospital

    Frederiksberg, 2000

Other trials in Denmark

Belgium3 sites
  • Cliniques universitaires saint-Luc

    Brussels, 1200

  • Algemeen Ziekenhuis Groeninge

    Kortrijk, West-vlaanderen, 8500

  • Universitaire Ziekenhuizen Leuven

    Leuven, 3000

Other trials in Belgium

Finland3 sites
  • Helsingin yliopistollinen keskussairaala, Meilahden sairaala

    Helsinki, 00290

  • Oulun yliopistollinen sairaala

    Oulu, 90220

  • Tampereen yliopistollinen Sairaala

    Tampere, 33520

Other trials in Finland

France1 site
  • Institut Gustave Roussy - Service d'Urologie

    Villejuif, 94805

Other trials in France

About this study

Official title: A PHASE 4, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF CONTINUED ENZALUTAMIDE TREATMENT BEYOND PROGRESSION IN PATIENTS WITH CHEMOTHERAPY-NAÏVE METASTATIC CASTRATION-RESISTANT PROSTATE CANCER

The purpose of this study is to determine if continued treatment with Enzalutamide is effective in patients with metastatic prostate cancer.

Conditions
Prostate Cancer
Being tested
Enzalutamide, Abiraterone, Placebo for Enzalutamide, Prednisone
Medical subject headings
Prostatic Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • EnzalutamideDrug

    Also called MDV3100, Xtandi

    160 mg by mouth once daily

  • AbirateroneDrug

    Also called Abiraterone acetate, Zytiga

    1000 mg by mouth once daily

  • Placebo for EnzalutamideDrug

    Sugar pill manufactured to mimic Enzalutamide 40 mg capsule

  • PrednisoneDrug

    Also called prednisolone

    5 mg by mouth twice daily

Study groups in NCT01995513
Study groupRoleWhat they receive
Enzalutamide & Abiraterone/prednisoneExperimentalEnzalutamide (160 mg) administered as four 40-mg capsules by mouth once daily in combination with abiraterone (1000 mg) administered as four 250-mg tablets by mouth once daily and prednisone (10 mg) administered as one 5-mg tablet by mouth twice daily
Receives: Drug: Enzalutamide; Drug: Abiraterone; Drug: Prednisone
Enzalutamide placebo & Abiraterone/prednisoneActive comparatorEnzalutamide placebo (placebo) capsules (identical in appearance to enzalutamide) administered as 4 capsules by mouth once daily in combination with abiraterone (1000 mg) administered as four 250-mg tablets by mouth once daily and prednisone (10 mg) administered as one 5-mg tablet by mouth twice daily.
Receives: Drug: Abiraterone; Drug: Placebo for Enzalutamide; Drug: Prednisone

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Progression Free Survival (PFS)

    PFS = time from randomization to first documentation of radiographic progression (RP),unequivocal clinical progression or death due to any cause (death within 112 days of treatment discontinuation without objective evidence of RP),whichever occurred first as per investigator. Unequivocal disease progression was pain requiring chronic administration of analgesics, decline of prostate cancer of Eastern Cooperative Oncology Group (ECOG) performance status score to 3 or higher or initiation of new anticancer therapy/radiation therapy or surgical intervention due to tumor progression. ECOG score range= 0(no severity) to 5(maximum severity).RP for bone disease was evaluated by appearance of 2 or more new bone lesions as per Prostate Cancer Clinical Trials Working Group 2 (PCWG2) or for soft tissue disease according to Response Evaluation Criteria in Solid Tumor version 1.1. Participants with no PFS event at analysis date were censored at last tumor assessment date prior to data cutoff date.

    Measured: From randomization until disease progression, last tumor assessment without disease progression or death due to any cause, whichever occurred first (maximum up to 20.3 months)

Secondary outcomes (12)
  1. Time to Prostate Specific Antigen (PSA) Progression

    Time from date of randomization to the date of first confirmed PSA progression as per Prostate Cancer Clinical Trials Working Group 2 (PCWG2). For participant's whose PSA decreased at Week 13 after randomization, progression was defined as 25 percent (%) PSA increase relative to nadir or absolute increase of >=2 nanogram/milliliter (ng/mL) above nadir. Progression was confirmed if another assessment measured at least 3 weeks later met the criterion as well. For participant's whose PSA did not decrease at Week 13 after randomization, progression was defined as 25% PSA increase relative to baseline assessed 12 weeks after baseline. Participants who were not known to have had a PFS event at the analysis date were censored at last PSA assessment date prior to data cutoff date.

    Measured: From randomization until disease progression, last tumor assessment without disease progression, whichever occurred first (maximum up to 11.1 months)

  2. Prostate Specific Antigen (PSA) Response Rate

    PSA response rate was defined as percentage of participants with >=30% and >=50% decrease in PSA from baseline at randomization to the maximal PSA response with a threshold of 30% and 50% respectively. PSA response was confirmed if another assessment measured at least 3 weeks later met the criterion as well.

    Measured: From randomization until disease progression, last tumor assessment without disease progression, whichever occurred first (maximum up to 11.1 months)

  3. Objective Response Rate (ORR)

    Objective response rate as assessed by the investigator according to Response Evaluation Criteria in Solid Tumor version 1.1 (RECIST v1.1) was defined as 1) Percentage of participants with confirmed best overall complete response (CR) and partial response (PR); 2) Percentage of participants with CR, PR and stable disease (SD) for target lesions or non-progressive disease for non-target lesions. CR: Disappearance of all non-nodal target and non-target lesions, including target and non-target lymph nodes reduction to <10 millimeter (mm) in short axis. No new lesions and disappearance of all non-target lesions. PR: >= 30% decrease in sum of diameters of target lesions, compared to the sum at baseline. The short axis was used in the sum for target nodes, while the longest diameter was used in the sum for all other target lesions.

    Measured: From randomization until CR or PR, whichever occurred first (maximum up to 21.3 months)

  4. Rate of Pain Progression

    Rate of pain progression was defined as percentage of participants with an increase of >=30% from baseline in the mean Brief Pain Inventory-Short Form (BPI-SF) pain intensity item scores of 4 items assessing average, worst, least, and intermediate pain severity. BPI-SF is an 11-item self-report questionnaire that is designed to assess the severity and impact of pain on daily functions of a participant. BPI-sf includes 4 questions that assess pain intensity (worst, least, average, right now) and 7 questions that assess impact of pain on daily functions (general activity, mood, walking ability, normal work, relations with other people, sleep, enjoyment of life). BPI-sf score range for each item was from 0=no pain to 10=worst possible pain. Total score was reported as average of individual questions ranges from 0 to 10, where lower scores indicated less pain or less pain interference.

    Measured: Month 6

  5. Time to First Use of New Antineoplastic Therapy for Prostate Cancer

    It was defined as time from randomization to the date of first use of subsequent antineoplastic therapy for prostate cancer. For participants who had not started subsequent antineoplastic therapy as of data analysis cutoff date, the time to first use of subsequent antineoplastic therapy was censored at the date of last assessment.

    Measured: From randomization until date of first use of any antineoplastic therapy (after last dose date of Period 2, maximum up to 22.3 months

  6. Change From Baseline in Quality of Life as Assessed by Functional Assessment of Cancer Therapy-Prostate (FACT-P) Global Score

    The FACT-P is a multidimensional, self-reported quality of life instrument consisting of 27 core items that assess participant function in 4 domains: physical, social/family, emotional, functional well-being, and supplemented by 12 site-specific items to assess for prostate-related symptoms. Each item is rated on a 0 to 4 Likert-type scale, and then combined to produce subscale scores for each domain, as well as a global quality of life score which is the sum of all 5 domain scores and ranges from 0 to 156 where higher scores represent better quality of life.

    Measured: Baseline, Week 9, 13, 17, 21, 25, 29, 33, 37, 41, 45, 49, 53, 57, 61, 65, 69, 73, 77, 81, 85, 89

  7. Change From Baseline in Quality of Life as Assessed by Functional Assessment of Cancer Therapy-Prostate (FACT-P) Social/Family Well-Being Domain Scores

    The FACT-P is a multidimensional, self-reported quality of life instrument consisting of 27 core items that assess participant function in 4 domains: physical, social/family, emotional, functional well-being, and supplemented by 12 site-specific items to assess for prostate-related symptoms. Each item is rated on a 0 to 4 Likert-type scale, and then combined to produce subscale scores for each domain. Total subscale score range for social/family well-being domain is from 0 (worst response) to 32 (best response), where higher score indicate better quality of life.

    Measured: Baseline, Week 9, 13, 17, 21, 25, 29, 33, 37, 41, 45, 49, 53, 57, 61, 65, 69, 73, 77, 81, 85, 89

  8. Change From Baseline in Quality of Life as Assessed by Functional Assessment of Cancer Therapy-Prostate (FACT-P) Emotional Well-Being Domain Scores

    The FACT-P is a multidimensional, self-reported quality of life instrument consisting of 27 core items that assess participant function in 4 domains: physical, social/family, emotional, functional well-being, and supplemented by 12 site-specific items to assess for prostate-related symptoms. Each item is rated on a 0 to 4 Likert-type scale, and then combined to produce subscale scores for each domain. Total subscale score range for emotional well-being domain is from 0 (worst response) to 24 (best response), where higher score indicate better quality of life.

    Measured: Baseline, Week 9, 13, 17, 21, 25, 29, 33, 37, 41, 45, 49, 53, 57, 61, 65, 69, 73, 77, 81, 85, 89

  9. Change From Baseline in Quality of Life as Assessed by Functional Assessment of Cancer Therapy-Prostate (FACT-P) Functional Well-Being Domain Scores

    The FACT-P is a multidimensional, self-reported quality of life instrument consisting of 27 core items that assess participant function in 4 domains: physical, social/family, emotional, functional well-being, and supplemented by 12 site-specific items to assess for prostate-related symptoms. Each item is rated on a 0 to 4 Likert-type scale, and then combined to produce subscale scores for each domain. Total subscale score range for functional well-being domain is from 0 (worst response) to 28 (best response), where higher score indicate better quality of life.

    Measured: Baseline, Week 9, 13, 17, 21, 25, 29, 33, 37, 41, 45, 49, 53, 57, 61, 65, 69, 73, 77, 81, 85, 89

  10. Change From Baseline in Quality of Life as Assessed by Functional Assessment of Cancer Therapy-Prostate (FACT-P) Prostate Cancer Domain Scores

    The FACT-P is a multidimensional, self-reported quality of life instrument consisting of 27 core items that assess participant function in 4 domains: physical, social/family, emotional, functional well-being, and supplemented by 12 site-specific items to assess for prostate-related symptoms. Each item is rated on a 0 to 4 Likert-type scale, and then combined to produce subscale scores for each domain. Total subscale score range for prostate cancer domain is from 0 (worst response) to 48 (best response), where higher score indicated better quality of life with fewer symptoms.

    Measured: Baseline, Week 9, 13, 17, 21, 25, 29, 33, 37, 41, 45, 49, 53, 57, 61, 65, 69, 73, 77, 81, 85, 89

  11. Change From Baseline in Quality of Life as Assessed by Functional Assessment of Cancer Therapy-Prostate (FACT-P) Physical Well-Being Domain Scores

    The FACT-P is a multidimensional, self-reported quality of life instrument consisting of 27 core items that assess participant function in 4 domains: physical, social/family, emotional, functional well-being, and supplemented by 12 site-specific items to assess for prostate-related symptoms. Each item is rated on a 0 to 4 Likert-type scale, and then combined to produce subscale scores for each domain. Total subscale score range for physical well-being domain is from 0 (worst response) to 28 (best response), where higher score indicate better quality of life.

    Measured: Baseline, Week 9, 13, 17, 21, 25, 29, 33, 37, 41, 45, 49, 53, 57, 61, 65, 69, 73, 77, 81, 85, 89

  12. Time to Degradation of the Functional Assessment of Cancer Therapy-Prostate (FACT-P) Global Score

    Time to degradation of FACT-P was defined as the time from randomization to first assessment with at least a 10-point decrease from baseline in the global FACT-P score for each participant. The FACT-P is a multidimensional, self-reported quality of life instrument consisting of 27 core items that assess participant function in 4 domains: physical, social/family, emotional, and functional well-being, and supplemented by 12 site-specific items to assess for prostate-related symptoms. Each item is rated on a 0 to 4 Likert-type scale, and then combined to produce subscale scores for each domain, as well as a global quality of life score which is the sum of all 5 domain scores and ranges from 0 to 156 with higher scores representing better quality of life. Participants with no score degradation at the time of analysis data cutoff were censored at the date of last assessment showing no degradation.

    Measured: From randomization up to maximum of 18.4 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Nov 2013 (estimated)
  2. Study start22 Oct 2013
  3. Primary completion15 Nov 2016
  4. Study completion31 Aug 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
509 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01995513
Sponsor's protocol ID
MDV3100-10
Other IDs
2013-000722-54, C3431013, PLATO, C3431013
Acronym
PLATO
Status last verified
Aug 2023
First submitted
18 Nov 2013
Last updated
18 Sep 2023
Data monitoring committee
No
Individual data sharing
Yes: Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical\_trials/trial\_data\_and\_results/data\_requests.

Publications

  • Attard G, Borre M, Gurney H, Loriot Y, Andresen-Daniil C, Kalleda R, Pham T, Taplin ME; PLATO collaborators. Abiraterone Alone or in Combination With Enzalutamide in Metastatic Castration-Resistant Prostate Cancer With Rising Prostate-Specific Antigen During Enzalutamide Treatment. J Clin Oncol. 2018 Sep 1;36(25):2639-2646. doi: 10.1200/JCO.2018.77.9827. Epub 2018 Jul 20.

    PubMed 30028657

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Enzalutamide, Abiraterone and Prednisone in people with Prostate Cancer, run by Pfizer at 95 sites in 11 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Sep 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 95 sites in Australia, Italy, Slovakia, Spain, United Kingdom and 6 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 17 Nov 2017). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Progression Free Survival (PFS) (time frame: From randomization until disease progression, last tumor assessment without disease progression or death due to any cause, whichever occurred first (maximum up to 20.3 months)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01995513, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Sep 2023.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in