Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

YL202 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 5 trials in our China and USA registers that name YL202 as an intervention. Synced 10 Nov 2026
5Current trials
4Recruiting now
1Lead sponsor
2Country registers
At a glance

YL202 is named as an intervention in 5 current clinical trials in our China and USA registers. 4 are recruiting patients now. The most common phase is Phase 3. The lead sponsor is MediLink Therapeutics (Suzhou) Co., Ltd. The most-studied condition is Non Small Cell Lung Cancer.

Patient leaflets for YL202

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

  • Recruiting480%
  • Active, closed120%

Trials by phase

  • Phase 3240%
  • Phase 1120%
  • Phase 2120%
  • Phase 1/2120%
01

Clinical trials of YL202

5 trials
StudyPhaseStatusLead sponsorRegisters
Pivotal Study to Evaluate YL202 Versus Docetaxel in Patients With Locally Advanced or Metastatic EGFR Sensitive Mutation Non-Squamous Non-Small Cell Lung Cancer
NCT07416994 · ClinicalTrials.gov ↗ · Non-Small Cell Lung Cancer
Phase 3 Recruiting MediLink Therapeutics (Suzhou) Co., Ltd China
YL202 Versus Treatment of Physician's Choice in Patients With HR+/HER2- Breast Cancer
NCT07461454 · ClinicalTrials.gov ↗ · Locally Advanced or Metastatic Breast Cancer
Phase 3 Recruiting MediLink Therapeutics (Suzhou) Co., Ltd China
A Study of YL202 in Patients With Advanced Solid Tumors
NCT07202364 · ClinicalTrials.gov ↗ · Non Small Cell Lung Cancer, Colorectal Cancer, Cervical Cancer
Phase 2 Recruiting MediLink Therapeutics (Suzhou) Co., Ltd China
A Study of YL202 in Combination With Other Anti-tumor Therapies in Patients With Advanced Solid Tumors
NCT07169994 · ClinicalTrials.gov ↗ · Advanced Solid Tumors, Breast Cancer, Non Small Cell Lung Cancer
Phase 1/2 Recruiting MediLink Therapeutics (Suzhou) Co., Ltd China
A Study of YL202 in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer and Breast Cancer
NCT05653752 · Non Small Cell Lung Cancer, Breast Cancer
Phase 1 Active, closed MediLink Therapeutics (Suzhou) Co., Ltd USA, 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 YL202

8 conditions
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
MediLink Therapeutics (Suzhou) Co., Ltd5
04

By country register

RegisterTrialsRecruiting
Clinical trials in China54
Clinical trials in USA10

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

05

Related compounds

06

Questions about YL202 trials

How many clinical trials are testing YL202?

5 current trials in our China and USA registers name YL202 as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are YL202 trials recruiting patients?

Yes. 4 of the 5 trials are recruiting: 4 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 YL202 clinical trials?

The lead sponsor is MediLink Therapeutics (Suzhou) 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 YL202 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 YL202 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 YL202 (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.