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Clinical Trials associated with NCR-101 / Not yet recruitingPhase 1/2 A Phase I/II, Open Label, Single Arm, Dose Escalation and Dose Expansion Clinical Trial to Evaluate the Safety, Tolerability and Efficacy of Human Induced Pluripotent Stem Cell Derived Mesenchymal Stromal Cells (NCR101) Injection 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.
/ Not yet recruitingPhase 1 评价NCR101注射液在间质性肺病患者中的安全性、耐受性和初步有效性的Ⅰ/Ⅱ期临床研究
[Translation] Phase I/II clinical study to evaluate the safety, tolerability and preliminary efficacy of NCR101 injection in patients with interstitial lung disease
主要目的:
Ⅰ期:评价NCR101注射液在间质性肺病患者中单次给药(SAD)和多次给药(MAD)的安全性和耐受性,确定临床用药的安全剂量。
次要目的:
Ⅰ期:评价NCR101注射液在间质性肺病患者中的初步有效性,为后续临床试验方案设计提供依据。
[Translation] Main purpose:
Phase I: To evaluate the safety and tolerability of single-dose (SAD) and multiple-dose (MAD) NCR101 injection in patients with interstitial lung disease, and to determine the safe dose for clinical use.
Secondary purpose:
Phase I: To evaluate the preliminary efficacy of NCR101 injection in patients with interstitial lung disease, and to provide a basis for the design of subsequent clinical trial programs.
100 Clinical Results associated with NCR-101
100 Translational Medicine associated with NCR-101
100 Patents (Medical) associated with NCR-101
100 Deals associated with NCR-101