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.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
22
ZH9 is a live attenuated S. enterica serovar Typhi ZH9 \[Ty2 ΔaroC ΔssaV\]), a differentiated novel microbial immunotherapy.
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
Incidence of dose-limiting toxicities
Toxicity will be evaluated according to the NCI CTCAE Version 5.0
Time frame: 28 days
Rate of complete pathologic response
Rate of complete pathologic response at determined timepoints by cystoscopy, urine cytology, and if needed for pathological confirmation, biopsy
Time frame: 3, 6, and 12 months
Rate of recurrence-free survival and duration or response
Rate of recurrence-free survival and duration of response as determined by cystoscopy and urine cytology
Time frame: 3, 6, and 12 months
Rate of CR
Rate of CR as determined by biopsy in patients with CIS at baseline
Time frame: 6 and 12 months
Proportion of patients with cystectomy-free survival
Proportion of patients with cystectomy-free survival as determined by cystoscopy and urine cytology
Time frame: 6 and 12 months
Rate of progression-free survival
Rate of progression-free survival, including disease progression and all-cause death
Time frame: 12 months
Overall response rate and recurrence-free rate
Overall response rate and recurrence-free rate in the bladder following IVI
Time frame: 6 and 12 months
Change from baseline in systemic and local inflammatory markers in the bladder
Change from baseline in systemic and local inflammatory markers in the bladder as defined by clinical laboratory safety assessments (serum chemistry, hematology, urinalysis)
Time frame: 12 months
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