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Clinical Trials/NCT05926583
NCT05926583
Active, not recruiting
Phase 3

Phase 3 Study to Evaluate the Safety and Efficacy of AAV5-hRKp.RPGR for the Treatment of Japanese X-linked Retinitis Pigmentosa Associated With Pathogenic Variants in Retinitis Pigmentosa GTPase Regulator (RPGR)

Janssen Pharmaceutical K.K.1 site in 1 country4 target enrollmentSeptember 12, 2023
InterventionsAAV5-hRKp.RPGR

Overview

Phase
Phase 3
Intervention
AAV5-hRKp.RPGR
Conditions
Not specified
Sponsor
Janssen Pharmaceutical K.K.
Enrollment
4
Locations
1
Primary Endpoint
Number of Participants with Abnormalities in Clinical Laboratory Assessments
Status
Active, not recruiting
Last Updated
19 days ago

Overview

Brief Summary

The purpose of the study is to assess the safety and tolerability of bilateral subretinal delivery of adeno-associated virus vector with a serotype 5 capsid human rhodopsin kinase promoter. retinitis pigmentosa guanosine triphosphatase regulator (AAV5-hRKp.RPGR).

Registry
clinicaltrials.gov
Start Date
September 12, 2023
End Date
November 12, 2030
Last Updated
19 days ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Participants who are Japanese male or female aged 5 years or older
  • Participants diagnosed as X-linked retinitis pigmentosa (XLRP) (generalized rod-cone dystrophy) associated with pathogenic or likely pathogenic variants in the retinitis pigmentosa guanosine triphosphatase regulator(RPGR) gene
  • Has evidence of preserved retinal function as defined by a mean retinal sensitivity of greater than or equal to (\>=) 2 decibel (dB) by Octopus static perimetry and evidence of preserved outer retinal structure (namely the presence of discernible ellipsoid zone) as determined by spectral domain-optical coherence tomography (SD-OCT) in both eyes
  • Otherwise, healthy participant on the basis of clinical laboratory tests performed at screening. If the results of the serum chemistry panel or hematology outside the normal reference ranges, the participant may be included only if the investigator judges the abnormalities or deviations from normal to be not clinically significant or to be appropriate and reasonable for the population under study. This determination must be recorded in the participant's source documents and initialed by the investigator

Exclusion Criteria

  • Has had ocular surgery within 3 months prior to screening or is anticipated to require ocular surgery within 6 months after the AAV5-hRKp.RPGR administration
  • Is unable to perform the imaging assessments as required (for example: reliable static perimetry \[reliability factor less than or equal to {\<=}19\], optical coherence tomography \[OCT\], or fundus autofluorescence \[FAF\]).
  • Any investigational ocular treatment or any other ocular treatment that could confound the interpretation of the efficacy results or affect participant compliance with the visit schedule

Arms & Interventions

Group 1: AAV5-hRKp.RPGR Low Dose

Participants will receive bilateral subretinal administration of AAV5-hRKp.RPGR low dose, with surgical delivery to the 2 eyes performed within 7 to 21 days apart.

Intervention: AAV5-hRKp.RPGR

Group 2: AAV5-hRKp.RPGR High Dose

Participants will receive bilateral subretinal administration of AAV5 hRKp.RPGR high dose, with surgical delivery to the 2 eyes performed within 7 to 21 days apart.

Intervention: AAV5-hRKp.RPGR

Outcomes

Primary Outcomes

Number of Participants with Abnormalities in Clinical Laboratory Assessments

Time Frame: Up to 60 Months

Number of participants with abnormalities in clinical laboratory assessment (hematology and serum chemistry) will be reported.

Number of Participants with Adverse Event (AEs)

Time Frame: Up to 60 Months

An AE is any untoward medical occurrence in a clinical study participant administered a investigational or non-investigational medicinal product. An AE does not necessarily have a causal relationship with the treatment.

Secondary Outcomes

  • Change From Baseline in Low Luminance Visual Acuity by Early Treatment Diabetic Retinopathy Study (ETDRS) Chart Letter Score in Monocular Assessment at Week 52(Baseline - Week 52)
  • Change From Baseline in Best Corrected Visual Acuity (BCVA) by Early Treatment Diabetic Retinopathy Study Chart Letter Score in Monocular Assessment at Week 52(Baseline - Week 52)
  • Change From Baseline in Low Luminance Visual Acuity by Early Treatment Diabetic Retinopathy Study Chart Letter Score in Worse-seeing Eye at Week 52(Baseline - Week 52)

Study Sites (1)

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