Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

GR2301 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our China register that name GR2301 as an intervention. Synced 10 Nov 2026
2Current trials
0Recruiting now
1Lead sponsor
1Country register
At a glance

GR2301 is named as an intervention in 2 current clinical trials in our China register. None are recruiting at the moment. All registered phases are Phase 1. The lead sponsor is Genrix (Shanghai) Biopharmaceutical Co., Ltd. The most-studied condition is Single Ascending Dose.

Patient leaflets for GR2301

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

  • Not yet open2100%

Trials by phase

  • Phase 12100%
01

Clinical trials of GR2301

2 trials
StudyPhaseStatusLead sponsorRegisters
A Study to Evaluate the Safety of GR2301 Injection in Healthy Volunteers.
NCT07190716 · ClinicalTrials.gov ↗ · Single Ascending Dose, Healthy Subjects
Phase 1 Not yet open Genrix (Shanghai) Biopharmaceutical Co., Ltd China
A Clinical Trial of Multiple Doses of GR2301 Injection in Healthy Adult Trial Participants in China.
NCT07647224 · ClinicalTrials.gov ↗ · Multiple Dose, Healthy Adult Participants
Phase 1 Not yet open Genrix (Shanghai) Biopharmaceutical Co., Ltd 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 GR2301

4 conditions
Single Ascending Dose1Healthy Subjects1Multiple Dose1Healthy Adult Participants1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Genrix (Shanghai) Biopharmaceutical Co., Ltd2
04

By country register

RegisterTrialsRecruiting
Clinical trials in China20

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

05

Questions about GR2301 trials

How many clinical trials are testing GR2301?

2 current trials in our China register name GR2301 as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are GR2301 trials recruiting patients?

Not at the moment. None of the 2 trials in our registers is recruiting; they are active but closed to enrolment, not yet open, or enrolling by invitation. Only the study team can confirm whether a patient is eligible.

Who sponsors GR2301 clinical trials?

The lead sponsor is Genrix (Shanghai) Biopharmaceutical Co., Ltd. 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 GR2301 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 GR2301 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 GR2301 (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.