Multicenter Clinical Trial of ST-02 for Ablation of Upper Tract Urothelial Carcinoma

What this study is about

The goal of this prospective clinical trial is to investigate the safety and efficacy of ST-02 (mucoadhesive gemcitabine suspension for pyelocaliceal instillation) to treat Upper Tract Urothelial Carcinoma (UTUC) in participants who have a low-grade tumor. The main questions this study aims to answer are: 1. Can ST-02 effectively eradicate UTUC by 3 months? 2. Is ST-02 safe for patients with UTUC? Participants in this study will receive ST-02, a new formulation with gemcitabine once weekly for six weeks. Gemcitabine is known to be an effective drug in treating urothelial carcinoma. This new formulation will be instilled directly into the upper urinary tract (renal pelvis) and will allow the chemotherapeutic to work locally for an extended period of time. The administration process will be retrograde (via a small catheter inserted up into the kidney, under anesthesia) or antegrade (via a nephrostomy, in the clinic) once weekly for six weeks. Safety and efficacy will be monitored for up to a year after the initial response assessment.

Who can join (things the study team will check)

✅ You may be able to join if…

• Adult (≥ 18 years) male or female
• Primary or recurrent low-grade (LG), noninvasive (Ta) Upper Tract Urothelial Carcinoma (UTUC) in the renal pelvis, infundibulum, and/or calyces, based on ureteroscopy, biopsy and cytology performed within 8 weeks prior to the Screening Visit
• At least 1 measurable papillary tumor measuring 5-15 mm
• Low grade tumor(s) in the ipsilateral ureter. Every attempt should be made to ablate this tumor completely, but residual ipsilateral ureteral tumor is not an exclusion criterion.
• Prior fully ablated low grade bladder tumor(s), without the need for intravesical therapy except for single-dose chemotherapy
• A life expectancy of greater than 12 months
• No active untreated urinary tract infection (UTI) as confirmed by urine culture or urinalysis
• Women of Child bearing potential (WoCBP) and Males who have a WoCBP partner require a negative pregnancy test at the Screening visit and must use two acceptable contraceptives methods until six months post-treatment
• All sexually active males must agree to use a condom during intercourse, for at least 48 h after each instillation

🚫 You may not be able to join if…

• Have received Bacillus Calmette - Guerin (BCG) treatment for UTUC within 6 weeks prior to Visit 1
• Pregnant (positive urine pregnancy test), planning pregnancy during trial, breast-feeding, or of childbearing potential without reliable contraception
• Unresolved infection requiring active treatment with systemic antimicrobial drugs
• History of high-grade non-muscle invasive bladder cancer within the past 6 months
• History of muscle-invasive bladder cancer during the past 2 years
• Actively being treated or intend to be treated with intravesical or systemic chemotherapy during the duration of the trial
• Urinary obstruction in the ipsilateral Upper Urinary Tract (UUT)
• Any contraindicated to gemcitabine or sensitivity to gemcitabine or any of the ST-02 ingredients
• Currently receiving another investigational agent or involved in a clinical trial with an investigational product within the past 30 days prior to Visit 1
• Active hepatitis B (chronic or acute) or active hepatitis C infection

Where this trial is running

• Vancouver Prostate Centre, Vancouver, British Columbia, Canada
• Men's Health Clinic, Winnipeg, Manitoba, Canada
• Centre of Applied Urology Research, Nova Scotia Health Authority, Halifax, Nova Scotia, Canada
• UHN - Princess Margaret Cancer Centre, Toronto, Ontario, Canada

Who to contact

Dasa Durkotova · 236 869 3437 · ddurkotova@prostatecentre.com

It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT06124976.