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Priya Life Science Compound trial record
Compound · clinical trials

LB4330 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our China register that name LB4330 as an intervention. Synced 9 Nov 2026
2Current trials
1Recruiting now
1Lead sponsor
1Country register
At a glance

LB4330 is named as an intervention in 2 current clinical trials in our China register. 1 is recruiting patients now. The most common phase is Phase 2/3. The lead sponsor is L & L Bio Co., Ltd., Ningbo, China. The most-studied condition is Cervical Cancer.

Patient leaflets for LB4330

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

  • Recruiting150%
  • Not yet open150%

Trials by phase

  • Phase 2/3150%
  • Phase 1/2150%
01

Clinical trials of LB4330

2 trials
StudyPhaseStatusLead sponsorRegisters
A Study to Evaluate LB1410 in Combination With LB4330 in Patients With Advanced or Metastatic Solid Tumors
NCT06468358 · ClinicalTrials.gov ↗ · Solid Tumor
Phase 1/2 Recruiting L & L Bio Co., Ltd., Ningbo, China China
Efficacy and Safety of LB1410 Plus Lenvatinib With or Without LB4330 in Advanced Recurrent/Metastatic Cervical Cancer
NCT07177716 · ClinicalTrials.gov ↗ · Cervical Cancer
Phase 2/3 Not yet open L & L Bio Co., Ltd., Ningbo, China 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 LB4330

2 conditions
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
L & L Bio Co., Ltd., Ningbo, China2
04

By country register

RegisterTrialsRecruiting
Clinical trials in China21

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

05

Related compounds

06

Questions about LB4330 trials

How many clinical trials are testing LB4330?

2 current trials in our China register name LB4330 as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are LB4330 trials recruiting patients?

Yes. 1 of the 2 trials is recruiting: 1 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 LB4330 clinical trials?

The lead sponsor is L & L Bio Co., Ltd., Ningbo, China. 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 LB4330 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 LB4330 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 LB4330 (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 9 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.