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Clinical Trial Summary

This is an open label, multi-center study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and preliminary efficacy of RAG-01 in patients with NMIBC who have failed BCG therapy.


Clinical Trial Description

The study is planned to include a "3+3" dose escalation phase. The primary study period includes a screening period, a treatment and Dose-Limiting Toxicity (DLT) assessment period, and a follow-up period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06351904
Study type Interventional
Source Ractigen Therapeutics.
Contact Long-Cheng Li
Phone +86 18051622388
Email lilc@ractigen.com
Status Recruiting
Phase Phase 1
Start date April 3, 2024
Completion date August 31, 2025

See also
  Status Clinical Trial Phase
Recruiting NCT06186414 - A Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of SIM0237 Alone or in Combination With BCG in NMIBC Phase 1
Active, not recruiting NCT03038321 - Solifenacin, Levofloxacin or Lornoxicam, Which Is Ideal for Management of Intravesical Instillation BCG Side Effects? Phase 4