SAR421869

DB17909InvestigationalGene Therapies

SAR421869 is a Lentiviral Vector Containing The Human My07A Gene currently being investigated for the treatment of retinitis pigmentosa associated with Usher syndrome 1B gene defect.

Code names
SAR421869

What you can answer from here — as of April 23, 2025

1Clinical trialPhase, status and sponsor resolved per trial
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Which companies are running trials of SAR421869, in which indications and phases, and which of those programs are still active?

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