drugset / Trial / NCT06663137

Open Label Study to Evaluate the Safety and Efficacy of NDV01 KIT in High Grade NMIBC

NCT06663137 ↗

Phase 2 Recruiting 70 enrolled Relmada Therapeutics, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a prospective, single-arm study evaluating the safety and efficacy of NDV01 KIT, a fixed-dose combination of gemcitabine HCl and docetaxel, administered via intravesical instillation in patients with high-grade Non-Muscle Invasive Bladder Cancer (NMIBC). NDV01 KIT includes 60 mL Carbopol Gel followed by 15 g NDV01 solution (gemcitabine HCl 1000 mg and docetaxel 40 mg), administered biweekly for six treatments, followed by monthly maintenance therapy for up to 12 months. The study includes a pharmacokinetic (PK) sub-study assessing systemic exposure to NDV01's active ingredients.

Timeline

Start
2024-08-01
Primary completion
2025-08
Completion
2026-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule 40 mg Intrathecal
Subject Gemcitabine Small molecule 1000 mg Intrathecal