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Single Ascending Dose Study in Participants With LCA10

← catalyst calendar

NCT03872479

Sponsored by Editas Medicine, Inc. (industry) · EDIT — their whole pipeline →.

Phase
Phase 1/2
Status
Unknown status
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
34estimated
Sites
5
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2019-09-26actualWhen the study began enrolling
Primary completion2025-05-23estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-05-23estimatedThe whole study's end, after follow-up
First posted2019-03-13actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2022-12-05actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Leber Congenital Amaurosis 10
  • Inherited Retinal Dystrophies
  • Eye Diseases, Hereditary
  • Retinal Disease
  • Retinal Degeneration
  • Vision Disorders
  • Eye Disorders Congenital

Intervention

  • Drug: EDIT-101

Primary outcomes

what the primary-completion date above is the date OF
Frequency of Adverse Events related to EDIT-101
measured 1 year
Number of participants experiencing procedural related adverse events
measured 1 year
Incidence of dose limiting toxicities
measured 1 year

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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