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Clinical Trial Summary

The principal aims of the clinical investigation involve assessing the safety profile and MTD of human forebrain neural progenitor cells (hNPC01) administered at escalated doses via single-dose intracerebral injection to subjects with stable chronic ischemic stroke.


Clinical Trial Description

The primary aims of this open-label single-armed study is to evaluate the safety and tolerability up to 4 cohorts of escalating doses of hNPC01 administered at a single dose via intracerebral injection to subjects with chronic cerebral ischemic stroke, and to determine MTD. The exploratory aim is to explore the evaluation tools with preliminary efficacy assessment and the potential of hNPC01 to mitigate the symptoms, especially motor symptoms associated with chronic stroke. Eligible participants for this study are individuals who have experienced a single ischemic stroke 6 to 60 months prior of enrollment and have exhibited no significant improvement following standard physical therapy interventions. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06299033
Study type Interventional
Source Hopstem Biotechnology Inc.
Contact Shuning Zhang, Ph.D
Phone +86 571-88197776
Email shuningzh@hopstem.com
Status Recruiting
Phase Phase 1
Start date November 9, 2023
Completion date December 30, 2025

See also
  Status Clinical Trial Phase
Recruiting NCT05694663 - Vagal Nerve Stimulation in Enhanced Stroke Recovery: The VALOR Registry
Completed NCT02448641 - Study of Modified Stem Cells (SB623) in Patients With Chronic Motor Deficit From Ischemic Stroke Phase 2
Completed NCT01287936 - A Study of Modified Stem Cells in Stable Ischemic Stroke Phase 1/Phase 2