Sponsor:
Merck Sharp & Dohme LLC
Code:
NCT06833073
Conditions
Urinary Bladder Neoplasms
Non-Muscle Invasive Bladder Neoplasms
Carcinoma in Situ
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Interventions
Intismeran autogene
BCG
Brief summary:
Conditions
Urinary Bladder Neoplasms
Non-Muscle Invasive Bladder Neoplasms
Carcinoma in Situ
Study ID
NCT06833073
Start date
Mar 11, 2025
Status verified date
Aug, 2026
Completion date
Sep 3, 2031
Anticipated
Primary completion date
Sep 3, 2031
Anticipated
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Enrollment
308 participants
Anticipated
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary purpose
Treatment
Arms
experimental: Intismeran autogene + BCG
active comparator: BCG
experimental: Intismeran autogene
Interventions
Intismeran autogene
BCG
Primary outcome measure
Central contacts
Locations
Michael G Oefelein Clinical Trials ( Site 0138)
Recruiting
Bakersfield, California, United States, 93301
Contacts
Study Coordinator
661-310-1063USC Norris Comprehensive Cancer Center ( Site 0123)
Recruiting
Los Angeles, California, United States, 90033
Contacts
Study Coordinator
800-872-2273Genesis Healthcare-Torrance ( Site 0140)
Recruiting
Torrance, California, United States, 90503
Contacts
Study Coordinator
310-542-0199Genesis Research LLC ( Site 0118)
Recruiting
Torrance, California, United States, 90505
Contacts
Study Coordinator
310-534-8400Urology Associates ( Site 0144)
Recruiting
Littleton, Colorado, United States, 80122
Contacts
Study Coordinator
303-733-8848Urological Research Network ( Site 0133)
Recruiting
Hialeah, Florida, United States, 33016
Contacts
Study Coordinator
786-431-2014Associated Urological Specialists - Chicago Ridge ( Site 0139)
Recruiting
Chicago Ridge, Illinois, United States, 60415
Contacts
Study Coordinator
708-566-6983Southern Urology, LLC ( Site 0145)
Recruiting
Lafayette, Louisiana, United States, 70508
Contacts
Study Coordinator
337-233-6665University of Missouri Health Care ( Site 0126)
Recruiting
Columbia, Missouri, United States, 65212
Contacts
Study Coordinator
573-882-7026NHO Revive Research Institute, LLC ( Site 0137)
Recruiting
Lincoln, Nebraska, United States, 68506
Contacts
Study Coordinator
402-484-4900Laura and Isaac Perlmutter Cancer Center at NYU Langone Health ( Site 0111)
Recruiting
New York, New York, United States, 10016
Contacts
Study Coordinator
646-960-1012TriState Urologic Services PSC Inc. dba The Urology Group ( Site 0122)
Recruiting
Cincinnati, Ohio, United States, 45212
Contacts
Study Coordinator
513-841-7700OHSU Knight Cancer Institute - South Waterfront ( Site 0110)
Recruiting
Portland, Oregon, United States, 97239
Contacts
Study Coordinator
503-494-4779MidLantic Urology ( Site 0102)
Recruiting
Bala-Cynwyd, Pennsylvania, United States, 19004
Contacts
Study Coordinator
610-667-0458The Conrad Pearson Clinic ( Site 0143)
Recruiting
Germantown, Tennessee, United States, 38138
Contacts
Study Coordinator
901-236-0957Texas Oncology-Austin Central ( Site 0107)
Recruiting
Austin, Texas, United States, 78705
Contacts
Study Coordinator
512-421-4235Urology Austin, PLLC ( Site 0109)
Recruiting
Austin, Texas, United States, 78759
Contacts
Study Coordinator
512-410-3773Urology of Virginia ( Site 0125)
Recruiting
Virginia Beach, Virginia, United States, 23462
Contacts
Study Coordinator
757-457-5100University of Washington - Fred Hutchinson Cancer Center ( Site 0100)
Recruiting
Seattle, Washington, United States, 98195
Contacts
Study Coordinator
206-598-3300The Moncton Hospital-Oncology ( Site 0200)
Recruiting
Moncton, New Brunswick, Canada, E1C 6Z8
Contacts
Study Coordinator
5068574780Centre intégré universitaire de santé et de services sociaux de l'Estrie - Centre Hospitalier Univer ( Site 0204)
Recruiting
Sherbrooke, Quebec, Canada, J1H 5N4
Contacts
Study Coordinator
8193461110Sponsor
Merck Sharp & Dohme LLC
Last update posted
Aug 26, 2026
Last verified
Aug, 2026
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Merck Sharp & Dohme LLC on 2026-08-26.