Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06936787

An Open-label, Dose-ascending Study of IGT001 for Retinitis Pigmentosa

A Prospective, Single-center, Open-label, Single Ascending Dose Study to Evaluate the Safety and Tolerability of Intravitreal Injection of IGT001 in Adult Patients With Retinitis Pigmentosa

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
21 (estimated)
Sponsor
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is an investigator-initiated, prospective, single-center, open-label, single ascending dose clinical study. The study aims to evaluate the safety, tolerability, and potential efficacy of intravitreal injection of IGT001 in patients with retinitis pigmentosa across different dose groups. IGT001 is administered as a single intravitreal injection in the study eye under local anesthesia. Participants will be discharged on the day of treatment, provided that their visual acuity and intraocular pressure are close to baseline levels, and no clinically significant abnormalities in vital signs are observed compared to pre-injection values. The decision for discharge will be determined by the investigator's assessment.

Detailed description

The study's dose groups are divided based on concentration into four cohorts: the low-concentration cohort (0.5 × 10⁶ hRP-50 µL), the medium-concentration cohort (1.0 × 10⁶ hRP-50 µL), the high-concentration cohort (2.0 × 10⁶ hRP-50 µL), and the target-concentration cohort. Participants in the four cohorts will undergo a one-year follow-up as specified in the protocol. They will also be encouraged to participate in an additional one-year follow-up study to assess the long-term safety and tolerability of IGT001 after completing the main study.

Conditions

Interventions

TypeNameDescription
DRUGIGT001Study drugs

Timeline

Start date
2025-04-20
Primary completion
2025-12-20
Completion
2027-12-20
First posted
2025-04-20
Last updated
2025-04-27

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06936787. Inclusion in this directory is not an endorsement.