Compound · clinical trials

TU2218 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our USA and South Korea registers that name TU2218 as an intervention. Synced 11 Nov 2026

2Current trials

2Recruiting now

1Lead sponsor

2Country registers

Maintained by Sreepriya Prasannan

MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany

Compiled from ClinicalTrials.gov registry records · Synced 11 Nov 2026 · Editorial standards

At a glance

TU2218 is named as an intervention in 2 current clinical trials in our USA and South Korea registers. 2 are recruiting patients now. All registered phases are Phase 1/2. The lead sponsor is TiumBio Co., Ltd. The most-studied condition is Advanced Solid Tumor.

Patient leaflets for TU2218

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 1/22100%

Clinical trials of TU2218

2 trials

Study	Phase	Status	Lead sponsor	Registers
Phase 1/2 Study of TU2218 Alone and in Combination With Checkpoint Inhibitors in Patients With Advanced Solid Tumors NCT05204862 · Advanced Solid Tumor	Phase 1/2	Recruiting	TiumBio Co., Ltd	USA, South Korea
Study of TU2218 in Combination With KEYTRUDA®(Pembrolizumab) in Patients With Advanced Solid Tumors NCT05784688 · Solid Tumor, Biliary Tract Cancer, Head and Neck Squamous Cell Carcinoma	Phase 1/2	Recruiting	TiumBio Co., Ltd	USA, South Korea

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.

Conditions studied with TU2218

5 conditions

Advanced Solid Tumor1 Solid Tumor1 Biliary Tract Cancer1 Head and Neck Squamous Cell Carcinoma1 Colorectal Cancer1

By country register

Register	Trials	Recruiting
Clinical trials in USA	2	2
Clinical trials in South Korea	2	2

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

Related compounds

Questions about TU2218 trials

How many clinical trials are testing TU2218?

2 current trials in our USA and South Korea registers name TU2218 as a drug or biological intervention, as of the registry sync on 11 November 2026. Completed and withdrawn studies are not counted.

Are TU2218 trials recruiting patients?

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

Who sponsors TU2218 clinical trials?

The lead sponsor is TiumBio 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 TU2218 works or whether it is effective, and it is not medical advice.

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 TU2218 works or whether it is effective. Each trial links to its own record so you can check it yourself.

ClinicalTrials.gov (U.S. National Library of Medicine) ↗ Trial IDs, titles, intervention names and synonyms, phase, overall status, lead sponsor and conditions for every trial on this page

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists TU2218 (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 11 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.