Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

RRG001 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our China register that name RRG001 as an intervention. Synced 10 Nov 2026
2Current trials
2Recruiting now
2Lead sponsors
1Country register
At a glance

RRG001 is named as an intervention in 2 current clinical trials in our China register. 2 are recruiting patients now. The most common phase is Phase 1/2. The sponsor with the most trials is Shanghai Refreshgene Technology Co., Ltd (1). The most-studied condition is Neovascular Age-related Macular Degeneration.

Patient leaflets for RRG001

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting2100%

Trials by phase

  • Phase 1/2150%
  • Early Phase 1150%
01

Clinical trials of RRG001

2 trials
StudyPhaseStatusLead sponsorRegisters
Safety and Efficacy of RRG001 Gene Therapy in Subjects With Neovascular Age-related Macular Degeneration (nAMD)
NCT06141460 · ClinicalTrials.gov ↗ · Neovascular Age-related Macular Degeneration
Phase 1/2 Recruiting Shanghai Refreshgene Technology Co., Ltd China
The Preliminary Safety and Efficacy of RRG001 After Vitrectomy in Subjects With Proliferative Diabetic Retinopathy (PDR)
NCT06412224 · ClinicalTrials.gov ↗ · PDR - Proliferative Diabetic Retinopathy
Early Phase 1 Recruiting Li Xiaorong China

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with RRG001

2 conditions
Neovascular Age-related Macular Degeneration1PDR - Proliferative Diabetic Retinopathy1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Shanghai Refreshgene Technology Co., Ltd1
Li Xiaorong1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China22

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about RRG001 trials

How many clinical trials are testing RRG001?

2 current trials in our China register name RRG001 as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are RRG001 trials recruiting patients?

Yes. 2 of the 2 trials are recruiting: 2 with sites in China. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors RRG001 clinical trials?

Shanghai Refreshgene Technology Co., Ltd (1) and Li Xiaorong (1). The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how RRG001 works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how RRG001 works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists RRG001 (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.