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Compound · clinical trials

Pembrolizumab/Finotonlimab

Also listed in trial records as PD-1 mAb
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our China register that name Pembrolizumab/Finotonlimab as an intervention. Synced 24 Sep 2026
2Trials tracked
1Recruiting now
2Lead sponsors
1Country register
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards

Pembrolizumab/Finotonlimab is named as a drug or biological intervention in 2 clinical trials in our China trial register, 1 of which is recruiting. Lead sponsors include Fudan University (1) and Ji Dongmei (1). Registered phases: Phase 2 and Phase 3. Conditions studied include Radioactive Iodine-refractory, Differentiated Thyroid Cancer With NRAS Mutation; Advanced PDTC or ATC With NRAS Mutation; Squamous Cell Carcinoma of Head and Neck.

01

Clinical trials of Pembrolizumab/Finotonlimab

2 trials
NCT IDStudyPhaseStatusLead sponsorRegister
NCT06970353 Phase II Trial of Tunlametinib in NRAS-Mutant Advanced Thyroid Cancer (ClinicalTrials.gov ↗)
Radioactive Iodine-refractory, Differentiated Thyroid Cancer With NRAS Mutation, Advanced PDTC or ATC With NRAS Mutation
Phase 2 Recruiting Fudan University China
NCT07509099 Cetuximab Combined With Pembrolizumab or Finotonlimab and Chemotherapy in R/M HNSCC (ClinicalTrials.gov ↗)
Squamous Cell Carcinoma of Head and Neck
Phase 3 Not yet open Ji Dongmei 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

3 conditions
Condition (as registered)Trials
Radioactive Iodine-refractory, Differentiated Thyroid Cancer With NRAS Mutation1
Advanced PDTC or ATC With NRAS Mutation1
Squamous Cell Carcinoma of Head and Neck1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Fudan University1
Ji Dongmei1
04

Trials by country register

RegisterPembrolizumab/Finotonlimab trials
Clinical trials in China2

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

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Pembrolizumab/Finotonlimab 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 Pembrolizumab/Finotonlimab (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 24 Sep 2026.

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 โ€” 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 โ€” we correct promptly and log it.