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NCT04278131RecruitingPhase 1/2

BS01 in Patients With Retinitis Pigmentosa

Phase 1/2, Safety and Efficacy Trial of BS01, a Recombinant Adeno-Associated Virus Vector Expressing ChronosFP in Patients With Retinitis Pigmentosa

Source: ClinicalTrials.gov · Last updated 23 Jan 2026

Brief summary (registry, in English)

A Phase 1/2, Safety and Efficacy Trial of BS01, a Recombinant Adeno-Associated Virus Vector Expressing ChronosFP (AAV2-CAG-ChronosFP) in Patients with Retinitis Pigmentosa

Status (registry)
Recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
20 (estimated)
First submitted
13 Feb 2020
Start date
6 Feb 2020
Primary completion date
30 Dec 2026
Lead sponsor
Bionic Sight LLC
NCT number
NCT04278131

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 20
  • From 6 Feb 2020 to the primary completion date, 30 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior receipt of any AAV gene therapy product

Other

  • Large amplitude nystagmus

Who the study is looking for

  • Confirmed diagnosis of retinitis pigmentosa
  • At least one eye with vision no better than 20/160 visual acuity on the EDTRS scale or, for patients with peripheral vision loss, a visual field no greater than 30°.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
New Jersey Retina
Coordinator of this site? Confirm its status
TeaneckUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.