drugset / Trial / NCT07264569

Evaluate the Safety, Tolerability, Biodistribution Characteristics and Preliminary Efficacy of BioTTT001

NCT07264569

Phase 1/2 Recruiting 42 enrolled Henan Cancer Hospital
NaSingle-groupOpen-labelTreatment

Summary

Phase Ib/II clinical study on evaluating the safety, tolerance, biodistribution characteristics and preliminary efficacy of recombinant human nsIL12 oncolytic adenovirus injection (BioTT001) in the treatment of meningeal metastasis in recurrent/progressive non-small cell lung cancer

Timeline

Start
2025-06-25
Primary completion
2027-12-30
Completion
2027-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject BioTTT001 Unknown 1e+09 vg Intrathecal
Subject BioTTT001 Unknown 5e+09 vg Intrathecal
Subject BioTTT001 Unknown 1e+10 vg Intrathecal