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A Phase 1/1b Study Evaluating the Safety, Pharmacology, and Clinical Effect of ZH9 Treatment in Patients With Non-Muscle Invasive Bladder Cancer
This is a first-in-human, multicenter, Phase 1/1b, 3-part, double-blind study of ZH9 in patients with recurrent NMIBC who are eligible for intravesical therapy. In Part 1, the safety, tolerability, and pharmacology of ZH9 IVI will be evaluated in a single ascending dose (SAD) patient cohort. In Part 2, the safety, tolerability, and pharmacology of ZH9 oral prime followed by ZH9 IVI will be evaluated in 2 patient cohorts at the doses and schedule established in Part 1. In Part 3, the safety, pharmacology, and clinical efficacy of ZH9 will be further evaluated in 2 expansion cohorts of patients with recurrent intermediate- and high-risk NMIBC.
Age
18 - 99 years
Sex
ALL
Healthy Volunteers
No
Michael G. Oefelein Clinical Trials
Bakersfield, California, United States
Duke Health-Duke Cancer Center
Durham, North Carolina, United States
Carolina Urologic Research Center, LLC
Myrtle Beach, South Carolina, United States
Urology San Antonio Medical Center
San Antonio, Texas, United States
Start Date
January 8, 2024
Primary Completion Date
August 30, 2025
Completion Date
July 30, 2027
Last Updated
August 19, 2025
22
ACTUAL participants
ZH9
DRUG
Lead Sponsor
Prokarium Ltd
NCT07339761
NCT03945162
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07122414