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A Trial to Evaluate the Safety, Tolerability and Preliminary Efficacy of NCR101 in the Treatment of Subjects With Interstitial Lung Disease

NCT06825169 PHASE1, PHASE2 NOT_YET_RECRUITING

The target of this trial is to evaluate the safety, tolerability and preliminary efficacy of NCR101 in the treatment of subjects with interstitial lung disease. The trial contains Single ascending dose(SAD) and Multiple ascending dose(MAD). Subjects will receive at least 1 dose of NCR101.

Details

Lead sponsorNuwacell Biotechnologies Co., Ltd.
PhasePHASE1, PHASE2
StatusNOT_YET_RECRUITING
Enrolment30
Start dateSat Mar 01 2025 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionFri Sep 01 2028 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions