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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05605964
Other study ID # MVT-601-056
Secondary ID
Status Active, not recruiting
Phase Phase 3
First received
Last updated
Start date January 25, 2023
Est. completion date December 31, 2024

Study information

Verified date May 2024
Source Sumitomo Pharma Switzerland GmbH
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This was a randomized study to evaluate the risk of major adverse cardiovascular events (MACE) for relugolix compared with leuprolide acetate. Enrollment in this study was discontinued by the Sponsor on 01 Dec 2023. In an effort to mitigate any treatment interruptions, actively enrolled patients will be allowed to remain on study drug up to a period of 12 months ending Dec 2024 if they choose to remain in the discontinuation phase of the study.


Description:

Eligible patients were randomized (1:1) to receive either relugolix or leuprolide acetate for prostate cancer or as an adjunct to primary or salvage radiation therapy. The study was intended to collect clinical and cardiovascular risk factor data on patients ages 18 and older who were receiving relugolix or leuprolide acetate for their prostate cancer or as adjunct to radiation therapy with a treatment plan to be on at least 12 months of continuous ADT. Enrollment in this study was discontinued by the Sponsor on 04 Dec 2023. In an effort to mitigate any treatment interruptions, actively enrolled patients will be allowed to remain on study drug up to a period of 12 months ending Dec 2024. During this discontinuation phase, all active investigative sites will be expected to formulate a transition plan for their study patients from this clinical study to SOC as soon as practicable. The primary endpoint in this study was the time to first adjudicated MACE (nonfatal myocardial infarction, nonfatal stroke, and cardiovascular death). However, with the discontinuation of enrollment in the study on 04 DEC 2023 by the sponsor, the primary endpoint will be to describe the safety of relugolix in the study population while actively enrolled patients remain on study drug.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 2250
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility A patient will be eligible for inclusion in the discontinuation phase of the study if the following applies: 1. Was previously enrolled under the original version and amendment 1 of this study 2. Has voluntarily resigned and dated the informed consent form prior to transition to the discontinuation phase of this study

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Relugolix
Relugolix tablet
Leuprolide Acetate
Leuprolide acetate injection

Locations

Country Name City State
United States Albany Medical College Albany New York
United States University of New Mexico Comprehensive Cancer Center Albuquerque New Mexico
United States Potomac Urology Center, PC Alexandria Virginia
United States Augusta University Augusta Georgia
United States Georgia Cancer Center Satellite Augusta Georgia
United States University Hospitals Seidman Cancer Center at UH Avon Health Center Satellite Avon Ohio
United States MidLantic Urology Bala-Cynwyd Pennsylvania
United States St. Vincent - Frontier Cancer Center Billings Montana
United States St. Vincent Healthcare Satellite Billings Montana
United States Illinois CancerCare - Bloomington Satellite Bloomington Illinois
United States St. Luke's Regional Medical Center Boise Idaho
United States St. Luke's Regional Medical Center Satellite Boise Idaho
United States Urology of Indiana, LLC Satellite Carmel Indiana
United States Oncology Specialists of Charlotte Charlotte North Carolina
United States Northwestern University Chicago Illinois
United States Swedish Hospital Satellite Chicago Illinois
United States Associated Urological Specialists Chicago Ridge Illinois
United States TriState Urologic Services PSC Inc. Cincinnati Ohio
United States University Hospitals Cleveland Medical Center Cleveland Ohio
United States Adult and Pediatric Urology P.C. Satellite Council Bluffs Iowa
United States Greater Regional Medical Center Creston Iowa
United States Advanced Urology Institute Daytona Beach Florida
United States Genesis Research, LLC Satellite Downey California
United States NorthShore University Health System - Evanston Hospital Evanston Illinois
United States Orange Coast Memorial Medical Center Fountain Valley California
United States St. Luke's Cancer Institute - Fruitland Satellite Fruitland Idaho
United States Central Ohio Urology Group Gahanna Ohio
United States Central Ohio Urology Group Satellite Gahanna Ohio
United States Illinois CancerCare - Galesburg Satellite Galesburg Illinois
United States NorthShore University Health System - Glenbrook Hospital Ambulatory Care Center Satellite Glenview Illinois
United States Altru Cancer Center Grand Forks North Dakota
United States Altru Health System Satellite Grand Forks North Dakota
United States Altru Professional Center Satellite Grand Forks North Dakota
United States Urology of Indiana, LLC Greenwood Indiana
United States Valley Cancer Associates Harlingen Texas
United States NorthShore University Health System - Highland Park Hospital Ambulatory Care Center Satellite Highland Park Illinois
United States Houston Metro Urology CRC, LLC Houston Texas
United States East Coast Institute for Research, LLC Jacksonville Florida
United States East Coast Institute for Research, LLC Satellite Jacksonville Florida
United States East Coast Institute for Research, LLC Satellite Jacksonville Florida
United States IU Health Arnett Cancer Center Lafayette Indiana
United States Comprehensive Urologic Care Lake Barrington Illinois
United States Lake City Cancer Center, LLC Lake City Florida
United States Keystone Urology Specialists Lancaster Pennsylvania
United States Arkansas Urology Little Rock Arkansas
United States Logan Regional Hospital Satellite Logan Utah
United States Genesis Research , LLC Los Alamitos California
United States Tower Urology Los Angeles California
United States University Hospitals Seidman Cancer Center at UH Mentor Health Center Satellite Mentor Ohio
United States St. Luke's Cancer Institute - Meridian Satellite Meridian Idaho
United States St. Luke's Meridian Medical Center Satellite Meridian Idaho
United States SG Research LLC Miami Florida
United States Helios CR, LLC Middleburg Heights Ohio
United States Urology Associates of Mobile Mobile Alabama
United States Pacific Cancer Care Monterey California
United States IU Health Ball Memorial Hospital Satellite Muncie Indiana
United States Intermountain Medical Center Satellite Murray Utah
United States Tri Valley Urology Medical Group Murrieta California
United States Tri Valley Urology Medical Group Satellite Murrieta California
United States Carolina Urologic Research Center Myrtle Beach South Carolina
United States St. Luke's Cancer Institute - Nampa Satellite Nampa Idaho
United States St. Luke's Nampa Medical Center Satellite Nampa Idaho
United States Urology Associates, P.C. Nashville Tennessee
United States Advanced Urology Associates New Lenox Illinois
United States Lowcountry Urology Clinics North Charleston South Carolina
United States McKay-Dee Hospital Satellite Ogden Utah
United States Adult and Pediatric Urology P.C. Omaha Nebraska
United States UH Minoff Health Center at Chagrin Highlands Orange Village Ohio
United States Lake Regional Health System Osage Beach Missouri
United States Illinois CancerCare - Ottawa Satellite Ottawa Illinois
United States Illinois CancerCare - Pekin Satellite Pekin Illinois
United States Capital Health Medical Center - Hopewell Pennington New Jersey
United States Illinois CancerCare, P.C. Peoria Illinois
United States Illinois CancerCare - Peru Satellite Peru Illinois
United States Utah Valley Hospital Provo Utah
United States Associated Urologists of North Carolina Raleigh North Carolina
United States Virginia Urology Richmond Virginia
United States Comprehensive Urology Royal Oak Michigan
United States St. George Regional Hospital Satellite Saint George Utah
United States Specialty Clinical Research of St. Louis Saint Louis Missouri
United States Urology of St. Louis Satellite Saint Louis Missouri
United States The Urology Place San Antonio Texas
United States Urology San Antonio Clinical Trials San Antonio Texas
United States San Bernadino Urological Associates Medical Group San Bernardino California
United States Genesis Research, LLC San Diego California
United States Guthrie Medical Group, PC Sayre Pennsylvania
United States Robert Packer Hospital Satellite Sayre Pennsylvania
United States Genesis Research, LLC Satellite Sherman Oaks California
United States Spokane Urology Spokane Washington
United States Associated Medical Professionals of NY, PLLC Syracuse New York
United States Florida Urology Partners, LLP Tampa Florida
United States Florida Urology Partners, LLP Satellite Tampa Florida
United States Florida Urology Partners, LLP Satellite Tampa Florida
United States Tri Valley Urology Medical Group Satellite Temecula California
United States Genesis Research, LLC Satellite Torrance California
United States Genesis Research, LLC Satellite Torrance California
United States Michigan Institute of Urology Troy Michigan
United States Arizona Urology Specialists, PLLC Tucson Arizona
United States St. Luke's Cancer Institute Satellite Twin Falls Idaho
United States St. Luke's Magic Valley Medical Center Satellite Twin Falls Idaho
United States Urology of Virginia Virginia Beach Virginia
United States Illinois CancerCare - Washington Satellite Washington Illinois
United States Medstar Washington Hospital Center Washington District of Columbia
United States Urologic Surgeons of Washington Washington District of Columbia
United States Wichita Urology Group Wichita Kansas
United States Wichita Urology Group Satellite Wichita Kansas
United States Wichita Urology Group Satellite Wichita Kansas
United States Potomac Urology Satellite Woodbridge Virginia

Sponsors (1)

Lead Sponsor Collaborator
Sumitomo Pharma Switzerland GmbH

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of Safety Outcomes Incidence of selective safety data including all serious adverse events, nonserious adverse events leading to discontinuation of relugolix or leuprolide acetate, and clinical laboratory tests as obtained per standard of care Screening; Day 1; 3, 6, 9, and 12 months; and every 3 months thereafter
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