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From:  Non-viral gene therapy for neuromuscular diseases including Duchenne muscular dystrophy using nanovesicles derived from human cells
Non-viral gene therapy for neuromuscular diseases including Duchenne muscular dystrophy using nanovesicles derived from human cells

Figure 1. Derived from human cells, nanovesicles are highly bio-friendly substance with excellent safety profiles as compared to foreign carriers. Allogeneic nanovesicles from diverse human cell sources are well-tolerated in human patients.

Rare Disease and Orphan Drugs Journal
ISSN 2771-2893 (Online)
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