AzTrials
AzTrials

Prostate CancerPhase 3PRONOUNCENCT02663908

A Trial Comparing Cardiovascular Safety of Degarelix Versus Leuprolide in Patients With Advanced Prostate Cancer and Cardiovascular Disease

A Phase 3 study testing Degarelix and Leuprolide in people with Prostate Cancer, run by Ferring Pharmaceuticals at 133 sites in 12 countries.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
Search all trials

Trial summary

The purpose of this trial is to test if a marketed drug for advanced prostate cancer (FIRMAGON) can reduce the risk of cardiovascular complications as compared to another marketed drug for advanced prostate cancer (LUPRON DEPOT) in subjects with prostate cancer and cardiovascular disease. Read more about this study

Who is it for?
Any age, men only
Conditions the study is for
Prostate Cancer
What is being tested?
Degarelix and Leuprolide
Could I receive a placebo?
No, everyone receives an active treatment
How many people
545 participants
Where
133 sitesin 12 countries
Study dates
19 Apr 2016to 29 Mar 2021
Phase
Phase 3
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 Any age
  • Men only
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Advanced prostate cancer
  • Indication to initiate androgen deprivation therapy (ADT)
  • Predefined cardiovascular disease

Who cannot join

  • Previous or current hormonal management of prostate cancer (unless terminated at least 12 months prior to trial)
  • Acute cardiovascular disease in the previous 30 days

Trial locations and contacts

133 sites in 12 countries.

133 sites in 12 countries

United States48 sites
  • Urology Group of New Mexico PC

    Albuquerque, New Mexico, 87109

  • Pacific Cancer Medical Center, Inc.

    Anaheim, California, 92801

  • Urologic Consultants of Southeaster PA LLP

    Bala-Cynwyd, Pennsylvania, 19004

  • Urology Center of Alabama PC

    Birmingham, Alabama, 35209

  • Seattle Urology Research Center

    Burien, Washington, 98166

  • Ralph H. Johnson VA Medical Center

    Charleston, South Carolina, 29401

  • Medical University of South Carolina (MUSC)

    Charleston, South Carolina, 29425

  • Erlanger Health System

    Chattanooga, Tennessee, 37403

  • Signal Point Clinical Research Center

    Dayton, Ohio, 45409

  • Urology Center of Colorado

    Denver, Colorado, 80211

  • Duke University Medical Center

    Durham, North Carolina, 27710

  • Advanced Urology Centers of New York Elmont Division

    Elmont, New York, 11003

  • Urology of Indiana LLC

    Greenwood, Indiana, 46032

  • First Urology PSC

    Jeffersonville, Indiana, 47130

  • University of Kansas Medical Center Research Institute, Inc.

    Kansas City, Kansas, 66160

  • San Diego Clinical Trials

    La Mesa, California, 91942

  • Comprehensive Urologic Care

    Lake Barrington, Illinois, 60010

  • Lancaster Urology

    Lancaster, Pennsylvania, 17604

  • Kansas City Urology Care

    Lenexa, Kansas, 66214

  • Clinical Trials Research

    Lincoln, California, 95648

  • Urology Associates, PA

    Little Rock, Arkansas, 72211

  • VA Greater Los Angeles Healthcare System

    Los Angeles, California, 90073

  • San Marcus Research Clinic Inc

    Miami, Florida, 33014

  • Mount Sinai Comprehensive Cancer Center

    Miami Beach, Florida, 33140

  • Clinical Research Solutions PC

    Middleburg Heights, Ohio, 44130

  • Medical College of Wisconsin, Inc.

    Milwaukee, Wisconsin, 53226

  • Delaware Valley Urology LLC Westhampton

    Mount Laurel, New Jersey, 08054

  • Yale University

    New Haven, Connecticut, 06519

  • Urology of Virginia

    Norfolk, Virginia, 23462

  • University of California, Irvine Medical Center

    Orange, California, 92868

  • University of Pennsylvania

    Philadelphia, Pennsylvania, 19104

  • Clinical Research Center of Florida

    Pompano Beach, Florida, 33060

  • Veterans Affairs Medical Center-Salisbury, NC

    Salisbury, North Carolina, 28144

  • University of Washington School of Medicine

    Seattle, Washington, 98195

  • Regional Urology, LLC

    Shreveport, Louisiana, 71106

  • Springfield Clinic LLP

    Springfield, Illinois, 62703

  • SUNY Upstate Medical University

    Syracuse, New York, 13210

  • Florida Urology Partners

    Tampa, Florida, 33615

  • Holy Name Medical Center

    Teaneck, New Jersey, 07666

  • Montefiore Medical Center PRIME

    The Bronx, New York, 10461

  • Skyline Urology

    Torrance, California, 90505

  • Chesapeake Urology Associates, P.A.

    Towson, Maryland, 21204

  • Arizona Institute of Urology

    Tucson, Arizona, 85704

  • Urological Associates of Southern Arizona

    Tucson, Arizona, 85715

  • University of Arizona College of Medicine

    Tucson, Arizona, 85724

  • Urologic Surgeons of Washington

    Washington D.C., District of Columbia, 20036

  • Iowa Clinic

    West Des Moines, Iowa, 50266

  • Innovative Clinical Research Institute

    Whittier, California, 90603

Other trials in United States

Slovakia15 sites
  • CUIMED s.r.o.

    Bratislava

  • Urocentrum Bratislava s.r.o.

    Bratislava

  • Nemocnica Kosice-Saca, a.s.

    Košice

  • Vychodoslovensky onkologicky ustav, a.s.

    Košice

  • Zeleznicna nemocnica Kosice

    Košice

  • UROCENTRUM LEVICE s.r.o.

    Levice

  • UROAMB s.r.o.

    Liptovský Mikuláš

  • Univerzitna nemocnica Martin

    Martin

  • Fakultna nemocnica Nitra

    Nitra

  • UROEXAM, spol. s r.o.

    Nitra

  • MILAB s.r.o.

    Prešov

  • MIRAMED s.r.o

    Rimavská Sobota

  • UROCENTRUM SALA s.r.o.

    Šaľa

  • Privatna Urologicka ambulancia

    Trenčín

  • Fakultna nemocnica s poliklinikou Zilina

    Žilina

Other trials in Slovakia

Germany12 sites
  • Gynaekologisches Zentrum Bonn-Friedensplatz

    Bonn

  • Staedtisches Klinikum Braunschweig GmbH - Standort Salzdahlumer

    Braunschweig, Lower Saxony

  • Staedtisches Klinikum Dresden Standort Dresden-Friedrichstadt

    Dresden, Saxony

  • Facharztpraxis für Urologie

    Eisleben Lutherstadt, Saxony-Anhalt

  • Universitaetsklinikum Freiburg

    Freiburg im Breisgau, Baden-Wurttemberg

  • Krankenhaus Martha-Maria Halle-Doelau

    Halle, Saxony-Anhalt

  • Urologische Gemeinschaftspraxis

    Herzogenaurach, Bavaria

  • Urologische Gemeinschaftspraxis

    Kirchheim unter Teck, Baden-Wurttemberg

  • Urologie am Nordplatz

    Leipzig, Saxony

  • Kliniken Maria Hilf GmbH

    Mönchengladbach, North Rhine-Westphalia

  • Praxisklinik Urologie Rhein Ruhr

    Mülheim, North Rhine-Westphalia

  • Klinikum Oldenburg gGmbH

    Oldenburg, Lower Saxony

Other trials in Germany

Canada10 sites
  • The Male Health Centre Euroscope Inc

    Barrie, Ontario

  • J. Giddens Medicine Professional Corporation

    Brampton, Ontario

  • G. Kenneth Jansz Medicine Professional Corporation

    Burlington, Ontario

  • Urology Associates Urologic Medical Research

    Kitchener, Ontario

  • Uro Laval

    Laval, Quebec

  • London Health Sciences Centre

    London, Ontario

  • Jewish General Hospital / McGill University

    Montreal, Quebec

  • Femalemale Health Centres

    Oakville, Ontario

  • CHU de Québec -Hôtel-Dieu de Québec

    Québec

  • Princess Margaret Cancer Centre

    Toronto, Ontario

Other trials in Canada

France10 sites
  • Institut Sainte Catherine

    Avignon

  • Groupe Hospitalier Pellegrin Tripode

    Bordeaux

  • Hôpital Henri Mondor

    Créteil

  • CHU de Grenoble - Hôpital Albert Michallon

    Grenoble

  • CH de Libourne- Hopital Robert Boulin

    Libourne

  • Hopital Claude Huriez - CHU Lille

    Lille

  • Hopital Edouard Herriot - CHU Lyon

    Lyon

  • Centre Hospitalier Régional Universitaire de Tours

    Nantes

  • Hopital Bichat - Claude Bernard

    Paris

  • Clinique Saint Jean Languedoc

    Toulouse

Other trials in France

Russia9 sites
  • City Clinical Hospital n.a. Botkin

    Moscow

  • FSBI "Moscow scientific research oncology institute"

    Moscow

  • FSBSI "Russian Oncological Scientific Center n.a. N.N. Blokhin"

    Moscow

  • SBEI HPE "Moscow State Medical and Dentistry University n.a. A. I. Evdokimov"

    Moscow

  • FBHI Privolzhskiy District Medical Centre FMBA of Russia

    Nizhny Novgorod

  • Medical Center Avitsenna

    Novosibirsk

  • BHI of Omsk region "Clinical Oncology Dispensary

    Omsk

  • FFSBI "The Nikiforov Russian Center of Emergency and Radiation Medicine"

    Saint Petersburg

  • SBHI of Sverdiovsk Region "Sverdiovsk Regional Clinical Hospital #1

    Yekaterinburg

Other trials in Russia

Czechia8 sites
  • Fakultni nemocnice Olomouc

    Olomouc

  • Fakultni nemocnice Ostrava

    Ostrava

  • Multiscan s.r.o.

    Pardubice

  • Urocentrum Plzen

    Pilsen

  • Fakultni nemocnice v Motole

    Prague

  • Proton Therapy Center Czech s.r.o.

    Prague

  • Oblastni nemocnice Pribram a.s.

    Příbram

  • Krajska zdravotni a.s. - Masarykova nemocnice v Usti nad Labem o.z.

    Ústí nad Labem

Other trials in Czechia

United Kingdom8 sites
  • Addenbrooke's Hospital

    Cambridge

  • St Peter's Hospital

    Chertsey, Surrey

  • Royal Devon and Exeter Hospital (Wonford)

    Exeter

  • Prince Philip Hospital

    Llanelli, Carmarthenshire

  • Charing Cross Hospital

    London, Greater London

  • Salford Royal

    Salford

  • Scunthorpe General Hospital

    Scunthorpe, Lincolnshire

  • Royal Hallamshire Hospital

    Sheffield, West Midlands

Other trials in United Kingdom

Greece6 sites
  • Central Clinic of Athens

    Athens

  • General Hospital of Athens "Alexandra"

    Athens

  • T.Y.P.E.T. Hygeias Melathron Hospital

    Athens

  • University General Hospital of Heraklion

    Heraklion

  • University of Patras Medical School

    Pátrai

  • General Hospital Papageorgiou

    Thessaloniki

Other trials in Greece

Poland4 sites
  • Swietokrzyskie Centrum Onkologii

    Kielce

  • DERMED Centrum Medyczne Sp. z o.o.

    Lodz

  • Provita Profamilia

    Piotrkow Trybunalski

  • WroMedica

    Wroclaw

Other trials in Poland

Finland2 sites
  • Keski-Suomen keskussairaala

    Jyväskylä

  • Tampereen yliopistollinen

    Tampere

Other trials in Finland

South Africa1 site
  • Groote Schuur Hospital Department of Urology

    Cape Town, Western Cape

Other trials in South Africa

About this study

Official title: A Multi-Center, Randomized, Assessor-Blind, Controlled Trial Comparing the Occurrence of Major Adverse Cardiovascular Events (MACEs) in Patients With Prostate Cancer and Cardiovascular Disease Receiving Degarelix (Gonadotropin-Releasing Hormone (GnRH) Receptor Antagonist) or Leuprolide (GnRH Receptor Agonist)

The purpose of this trial is to test if a marketed drug for advanced prostate cancer (FIRMAGON) can reduce the risk of cardiovascular complications as compared to another marketed drug for advanced prostate cancer (LUPRON DEPOT) in subjects with prostate cancer and cardiovascular disease.

Conditions
Prostate Cancer
Being tested
Degarelix, Leuprolide
Medical subject headings
Prostatic Neoplasms

What participants receive

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

  • DegarelixDrug

    Also called FIRMAGON

  • LeuprolideDrug

    Also called LUPRON DEPOT

Study groups in NCT02663908
Study groupRoleWhat they receive
DegarelixExperimentalNot described
Receives: Drug: Degarelix
LeuprolideActive comparatorNot described
Receives: Drug: Leuprolide

What is being measured

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

  1. Time From Randomization to the First Confirmed (Adjudicated) Occurrence of the Composite Major Adverse Cardiovascular Event (MACE) Endpoint; Percentage of Observed Subjects With Outcome Measure Events During the Trial

    Composite MACE endpoint was defined as: death due to any cause, non-fatal myocardial infarction or non-fatal stroke.

    Kaplan Meier plots of the cumulative incidence rate by treatment groups were used to depict first confirmed (adjudicated) occurrence of composite MACE over time. Percentage of observed subjects with outcome measure events during the trial are reported.

    Subjects were censored at the time a subject discontinued the trial, was lost to follow-up, discontinued treatment with IMP, initiated treatment with prohibited medication (including hormonal combination therapy), or at Day 336, whichever occurred first.

    Measured: Randomization to Day 336 (end-of-trial)

Secondary outcomes (18)
  1. Time From Randomization to the First Confirmed (Adjudicated) Occurrence of Cardiovascular (CV)-Related Death, Non-fatal Myocardial Infarction or Non-fatal Stroke; Percentage of Observed Subjects With Outcome Measure Events During the Trial

    Kaplan Meier plots of the cumulative incidence rate by treatment groups were used to depict confirmed (adjudicated) occurrence of CV-related death, non-fatal myocardial infarction or non-fatal stroke. Percentage of observed subjects with outcome measure events during the trial are reported.

    Subjects were censored at the time a subject discontinued the trial, was lost to follow-up, discontinued treatment with IMP, initiated treatment with prohibited medication (including hormonal combination therapy), or at Day 336, whichever occurred first.

    Measured: Randomization to Day 336 (end-of-trial)

  2. Time From Randomization to Confirmed (Adjudicated) CV-related Death; Percentage of Observed Subjects With Outcome Measure Events During the Trial

    Kaplan Meier plots of the cumulative incidence rate by treatment groups were used to depict confirmed (adjudicated) CV-related death. Percentage of observed subjects with outcome measure events during the trial are reported. Percentage of observed subjects with outcome measure events during the trial are reported.

    Subjects were censored at the time a subject discontinued the trial, was lost to follow-up, discontinued treatment with IMP, initiated treatment with prohibited medication (including hormonal combination therapy), or at Day 336, whichever occurred first.

    Measured: Randomization to Day 336 (end-of-trial)

  3. Time From Randomization to the First Confirmed (Adjudicated) Myocardial Infarction; Percentage of Observed Subjects With Outcome Measure Events During the Trial

    Kaplan Meier plots of the cumulative incidence rate by treatment groups were used to depict first confirmed (adjudicated) myocardial infarction. Percentage of observed subjects with outcome measure events during the trial are reported.

    Subjects were censored at the time a subject discontinued the trial, was lost to follow-up, discontinued treatment with IMP, initiated treatment with prohibited medication (including hormonal combination therapy), or at Day 336, whichever occurred first.

    Measured: Randomization to Day 336 (end-of-trial)

  4. Time From Randomization to the First Confirmed (Adjudicated) Stroke; Percentage of Observed Subjects With Outcome Measure Events During the Trial

    Kaplan Meier plots of the cumulative incidence rate by treatment groups were used to depict first confirmed (adjudicated) stroke. Percentage of observed subjects with outcome measure events during the trial are reported.

    Subjects were censored at the time a subject discontinued the trial, was lost to follow-up, discontinued treatment with IMP, initiated treatment with prohibited medication (including hormonal combination therapy), or at Day 336, whichever occurred first.

    Measured: Randomization to Day 336 (end-of-trial)

  5. Time From Randomization to the First Confirmed (Adjudicated) Unstable Angina Requiring Hospitalization; Percentage of Observed Subjects With Outcome Measure Events During the Trial

    Kaplan Meier plots of the cumulative incidence rate by treatment groups were used to depict first confirmed (adjudicated) unstable angina requiring hospitalization. Percentage of observed subjects with outcome measure events during the trial are reported.

    Subjects were censored at the time a subject discontinued the trial, was lost to follow-up, discontinued treatment with IMP, initiated treatment with prohibited medication (including hormonal combination therapy), or at Day 336, whichever occurred first.

    Measured: Randomization to Day 336 (end-of-trial)

  6. Time From Randomization to Death Due to Any Cause; Percentage of Observed Subjects With Outcome Measure Events During the Trial

    Kaplan Meier plots of the cumulative incidence rate by treatment groups were used to depict death due to any cause. Percentage of observed subjects with outcome measure events during the trial are reported.

    Subjects were censored at the time a subject discontinued the trial, was lost to follow-up, discontinued treatment with IMP, initiated treatment with prohibited medication (including hormonal combination therapy), or at Day 336, whichever occurred first.

    Measured: Randomization to Day 336 (end-of-trial)

  7. Testosterone Levels at Days 28, 168 and 336 in the Degarelix and Leuprolide Treatment Groups

    Median levels and interquartile ranges for serum testosterone at Days 28, 168, and 336 are presented.

    Measured: Days 28, 168 and 336 (end-of-trial)

  8. Time From Randomization to Failure in Progression-free Survival (PFS); Percentage of Observed Subjects With Outcome Measure Events During the Trial

    Time to failure in PFS was defined as the time, measured in days, from randomization to the first occurrence of either death, radiographic disease progression, introduction of additional prostate cancer therapies for progression, or PSA failure.

    Subjects who discontinued treatment with IMP or withdrew from the trial were censored at the time of discontinuation/withdrawal.

    Kaplan Meier plots of the cumulative incidence rate by treatment groups were used to depict failure in PFS. Percentage of observed subjects with outcome measure events during the trial are reported.

    Measured: From randomization to end-of-trial for each subject (subjects not censored at Day 336)

  9. Changes From Baseline in International Prostate Symptom Score (IPSS) Total and Quality of Life (QoL) Scores

    Lower urinary tract symptoms were measured with the IPSS Version 1 (IPSS-1). The IPSS is a subject-administered questionnaire containing seven items to evaluate symptoms of urinary obstruction (incomplete emptying, frequency, intermittency, urgency, weak stream, straining, nocturia) over the preceding week. Each urinary symptom question was assigned points from 0 to 5 indicating increasing severity of the particular symptom. The total IPSS-1 score was then calculated as summation over the responses for all 7 questions. The total IPSS-1 score was transformed to a scale from 0 (lowest score) to 100 (highest score). Higher scores reflect higher severity of symptoms. The IPSS-1 included an additional single question to assess a subject's QoL in relation to his urinary symptoms; response to this question was analyzed separately and was not included in the total IPSS score. The score was similarly scaled from 0 to 100.

    Change from baseline in IPSS Total and QoL scores are presented.

    Measured: Baseline to Days 168 and 336 (end-of-trial)

  10. Total Number of CV-related Hospitalization Events Over the Duration of the Trial

    The total number of CV-related hospitalizations over the duration of the trial was defined as the number of hospitalizations due to CV-related adverse events, observed from the first exposure to IMP up until Day 336 for each subject.

    Measured: First dose of IMP to Day 336 (end-of-trial)

  11. Total Number of Coronary Artery By-pass Grafting (CABG) or Percutaneous Coronary Intervention (PCI) Procedures Over the Duration of the Trial

    The total number of CABG or PCI procedures observed for each subject over the duration of the trial

    Measured: First dose of IMP to Day 336 (end-of-trial)

  12. Total Number of CV-related Emergency Room (ER) Visit Events Over the Duration of the Trial

    CV-related ER visit events (that did not lead to hospitalization) was observed from the first exposure to IMP up until Day 336 for each subject.

    Measured: First dose of IMP to Day 336 (end-of-trial)

  13. Change in Utility, Based on EuroQol Group 5 Dimensions 5 Levels Questionnaire (EQ-5D-5L)

    The EQ-5D-5L essentially consists of 2 systems - the EQ-5D-5L descriptive system and the EQ visual analogue scale (EQ VAS). The EQ-5D-5L descriptive system comprises the following 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. The EQ VAS is an overall estimation of the present health status. The results from the EQ-5D-5L questionnaire were converted into quality adjusted life year (QALY) units.

    The QALY is estimated by combining the value of life (utility value) and length of life. Quality adjusted life years are based on a principle assuming that a year of life lived in perfect health is worth 1 QALY and that a year of life lived in a state of less than perfect health is worth less than 1.

    Measured: Baseline to Day 336 (end-of-trial)

  14. Changes From Baseline in Duke Activity Status Index (DASI) Global Score

    The DASI is a self-administered instrument developed to measure functional capacity in subjects with cardiovascular disease (CVD). It contains 12 items referring to the present time, assessing the ability to perform physical tasks in five domains: personal care (1 item), ambulation (4 items), household tasks (4 items), sexual function (1 item) and recreation (2 items). Each question was answered by one of four options: 'yes with no difficulty' / 'yes, but with some difficulty' / 'no, I can't do this' / 'don't do this for other reasons'. A global score was calculated with a higher score indicating a higher functional capacity. The minimum score is 0 and the maximum score is 58.2 points.

    Change from baseline in DASI Global score is presented.

    Measured: Baseline to Days 168 and 336 (end-of-trial)

  15. Changes From Baseline in Cardiac Anxiety Questionnaire (CAQ) Global Score and Score Per Domain

    The CAQ is a self-administered questionnaire developed to measure heart-focused anxiety in persons with or without heart disease. It contains 18 items referring to the present time assessing cardiac anxiety in three domains: fear (8 items, each item could be scored between 0 "never" to 4 "always", maximum total score 32), avoidance (5 items, each item could be scored between 0 "never" to 4 "always", maximum total score 20) and attention (5 items, each item could be scored between 0 "never" to 4 "always", maximum total score 20). A higher score indicated greater cardiac anxiety and the total score range was between 0 and 72.

    Change from baseline in CAQ Global score and score per domain are presented.

    Measured: Baseline to Days 168 and 336 (end-of-trial)

  16. Number of Subjects With Adverse Events (AEs)

    Adverse events were recorded from signed informed consent until end-of-trial. Adverse events with onset after start of IMP treatment, and within 3 months after (1 month=28 days) last dosing of IMP, were considered 'treatment-emergent' and are presented for the safety analysis set.

    Measured: Start of IMP treatment until 3 months after last dosing of IMP

  17. Intensity of AEs

    The intensity of AE was graded using the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) (version 4.02) 5-point scale.

    AE were categorized as grade 1 Mild (minor; no specific medical intervention; asymptomatic laboratory findings only; marginal clinical relevance), Grade 2 Moderate (minimal intervention: local intervention; non-invasive intervention), Grade 3 Severe (significant symptoms, requiring hospitalization or invasive intervention; transfusion; elective interventional radiological procedure; therapeutic endoscopy or operation), Grade 4 Life-threatening or disabling (complicated by acute, life-threatening metabolic or CV complications such as circulatory failure, hemorrhage, sepsis. Life-threatening physiologic consequences; need for intensive care or emergent invasive procedure; emergent interventional radiological procedure, therapeutic endoscopy or operation) and Grade 5 Death. Events with grades 3, 4 and 5 were categorized as severe.

    Measured: Start of IMP treatment until 3 months after last dosing of IMP

  18. Changes in Vital Signs

    Number of subjects shifting from normal value(s) in vital signs (pulse and blood pressure) at baseline to clinically significant abnormal value(s) at end-of-trial are presented.

    Note: Only subjects with appropriate baseline and post-baseline data are included in the evaluation.

    Measured: Baseline to Day 336 (end-of-trial)

Timeline

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

  1. First posted26 Jan 2016 (estimated)
  2. Study start19 Apr 2016
  3. Primary completion29 Mar 2021
  4. Study completion29 Mar 2021

Why it stopped: Recruitment rate; a lower than anticipated observed cardiovascular event rate. The Sponsor decision to stop the trial was not based on any safety concerns or any knowledge of the results, or influenced by issues imposed by the COVID-19 pandemic.

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 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
545 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02663908
Sponsor's protocol ID
000108
Acronym
PRONOUNCE
Status last verified
May 2022
First submitted
22 Jan 2016
Last updated
29 Jun 2022
Data monitoring committee
Yes

Publications

  • Lopes RD, Higano CS, Slovin SF, Nelson AJ, Bigelow R, Sorensen PS, Melloni C, Goodman SG, Evans CP, Nilsson J, Bhatt DL, Clarke NW, Olesen TK, Doyle-Olsen BT, Kristensen H, Arney L, Roe MT, Alexander JH; PRONOUNCE Study Investigators. Cardiovascular Safety of Degarelix Versus Leuprolide in Patients With Prostate Cancer: The Primary Results of the PRONOUNCE Randomized Trial. Circulation. 2021 Oct 19;144(16):1295-1307. doi: 10.1161/CIRCULATIONAHA.121.056810. Epub 2021 Aug 30.

    PubMed 34459214
  • Melloni C, Slovin SF, Blemings A, Goodman SG, Evans CP, Nilsson J, Bhatt DL, Zubovskiy K, Olesen TK, Dugi K, Clarke NW, Higano CS, Roe MT; PRONOUNCE Investigators. Cardiovascular Safety of Degarelix Versus Leuprolide for Advanced Prostate Cancer: The PRONOUNCE Trial Study Design. JACC CardioOncol. 2020 Mar 17;2(1):70-81. doi: 10.1016/j.jaccao.2020.01.004. eCollection 2020 Mar.

    PubMed 34396210
  • Zengerling F, Jakob JJ, Schmidt S, Meerpohl JJ, Blumle A, Schmucker C, Mayer B, Kunath F. Degarelix for treating advanced hormone-sensitive prostate cancer. Cochrane Database Syst Rev. 2021 Aug 5;8(8):CD012548. doi: 10.1002/14651858.CD012548.pub2.

    PubMed 34350976

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Degarelix and Leuprolide in people with Prostate Cancer, run by Ferring Pharmaceuticals at 133 sites in 12 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 3 inclusion and 2 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: stopped early, as of the sponsor's last update on 29 Jun 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 133 sites in United States, Slovakia, Germany, Canada, France and 7 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 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

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 29 Jun 2022). 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?

Time From Randomization to the First Confirmed (Adjudicated) Occurrence of the Composite Major Adverse Cardiovascular Event (MACE) Endpoint; Percentage of Observed Subjects With Outcome Measure Events During the Trial (time frame: Randomization to Day 336 (end-of-trial)). 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 NCT02663908, which also lists 3 linked publications.

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 29 Jun 2022.

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