Last reviewed · How we verify
A Trial to Evaluate the Safety, Tolerability and Preliminary Efficacy of NCR101 in the Treatment of Subjects With Interstitial Lung Disease
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 sponsor | Nuwacell Biotechnologies Co., Ltd. |
|---|---|
| Phase | PHASE1, PHASE2 |
| Status | NOT_YET_RECRUITING |
| Enrolment | 30 |
| Start date | Sat Mar 01 2025 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Fri Sep 01 2028 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Interstitial Lung Disease (ILD)
Interventions
- NCR101 injection