A Phase 2b Study of UGN-102 for Low Grade Intermediate Risk Non-Muscle-Invasive Bladder Cancer

Inclusion Criteria

• •1. Willing and able to sign an informed consent and comply with the protocol.
• •2. Has newly diagnosed or historic LG NMIBC (Ta) histologically confirmed by cold cup biopsy at screening or within 6 weeks of screening.
• •3. Is at intermediate risk of recurrence, defined as having 1 or 2 of the following:
• •* Presence of multiple tumors;
• •* Solitary tumor \> 3 cm;
• •* Recurrence (≥ 1 occurrence of LG NMIBC within 1 year of the current diagnosis).
• •4. Has negative voiding cytology for high grade (HG) disease at or within 6 weeks of enrollment.
• •5. Willing to use 2 acceptable forms of effective contraception from enrollment through 6 months post treatment if the participant is female or the female partner of a male participant and is of childbearing potential (defined as premenopausal women who have not been sterilized).
• •6. Has adequate organ and bone marrow function as determined by routine laboratory tests as below:
• •* Leukocytes ≥ 3,000 per μL;
• •* Absolute neutrophil count ≥ 1,500 per μL;
• •* Platelets ≥ 100,000 per μL;
• •* Hemoglobin ≥ 9.0 g/dL;
• •* Total bilirubin ≤ 1.5 x upper limit of normal (ULN);
• •* Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN;
• •* Alkaline phosphatase ≤ 2.5 × ULN;
• •* Estimated glomerular filtration rate (eGFR) ≥ 30 mL/min.
• •7. Has no evidence of active urinary tract infection (UTI) at Screening and Baseline visits.
• •* In the case of symptomatic UTI, the patient will be treated with a full course of antibiotics, and study drug will be postponed until resolution. In the case of asymptomatic bacteriuria, the use of prophylactic antibiotics and postponement of study drug is left to the discretion of the Principal Investigator (PI).