Table 1.
Name | Initial source | Processing method | Cell source | Preclinical studies evidence | Clinical trials | Disease | Limitations | References |
---|---|---|---|---|---|---|---|---|
CTX0E3 | Allogeneic | Transfection with c-mycER | Immortalizing human neural stem cell line | Neurogenesis and angiogenesis (exosome) | NCT01151124 | Chronic ischemic stroke | Long period recovery after enrollment | Stroemer et al., 2009; Kalladka et al., 2016 |
NT2N | Allogeneic | Neuronal phenotype in vitro following retinoic acid treatment | Clonal human teratocarcinoma cell line | Dopaminergic phenotypes | Nelson et al. (2002) | PD, HD, trauma | Tumor formation experienced; apoptotic-like cell death; negligible therapeutic influence for stroke | Borlongan et al., 1998; Hurlbert et al., 1999; Baker et al., 2000; Nelson et al., 2002 |
SB623 | Allogeneic | Transfection expression vector containing Notch-1 intracellular domain | Bone marrow- derived mesenchymal stem cells | Neurotrophic, angiogenic, and neuroprotective effects | NCT01287936 | Chronic stable stroke & trauma | Less studies and trials; nonrandomized design | Dezawa et al., 2004; Steinberg et al., 2016 |
NSI-566 | Allogeneic | A single fetal spinal cord without genetic modification | Primary adherent human neural stem cell line | Integrate with host tissues; Immunosuppressive effects | NCT03296618 | Amyotrophic lateral sclerosis, spinal cord injury | Less clinical trials | Glud et al., 2016; Curtis et al., 2018; Zhang et al., 2019a |
c-mycER: c-myc gene fused with a mutated estrogen receptor; HD: Huntington’s disease; PD: Parkinson’s disease.