Status and phase
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About
To evaluate the efficacy of ZA oral solution in subjects with IRD caused by biallelic recessive RPE65 or LRAT gene mutations and phenotypically diagnosed as Leber's Congenital Amaurosis (LCA) or Retinitis Pigmentosa (RP).
Sex
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Inclusion criteria
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Primary purpose
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Interventional model
Masking
0 participants in 3 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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