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NCT03975543: PHENOROD1

Retrospective Natural History Study of Retinitis Pigmentosa

Status unknown Last updated 4 August 2021
What this trial tests

trial in Retinitis Pigmentosa (RP) in 113 participants. Status unknown.

Timeline
1 October 2018
Primary endpoint
1 October 2019
30 September 2021

Quick facts

Lead sponsorSparingVision
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment113
Start date1 October 2018
Primary completion1 October 2019
Estimated completion30 September 2021
Sites1 location across France

Conditions studied

Sponsor

SparingVision — full company profile →

Who can join

Eligibility, any sex, with Retinitis Pigmentosa (RP). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is natural history study of rods and cones degenerations in patients with Retinitis Pigmentosa (RP) caused by pathogenic mutations in RHO, PDE6A or PDE6B gene mutations.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Moving Towards PDE6A Gene Supplementation Therapy.
    Bujakowska KM, Comander J. · · 2020 · cited 1× · PMID 33057571 · DOI 10.1001/jamaophthalmol.2020.4216

Verify or expand the search:

Other recruiting trials for Retinitis Pigmentosa (RP)

Currently open trials in the same condition.

Other SparingVision trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03975543.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing