CI

At a glance

ClinicalIndex Comparison Record
Phase 3Recruiting· 30 target
Drug / intervention
Capmatinibdrug
Likely dose
Capmatinib 800 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06988475
NCT06988475Phase 3RecruitingOn TrackUpdated 7mo ago

DETERMINE (Determining Extended Therapeutic Indications for Existing Drugs in Rare Molecularly Defined Indications Using a National Evaluation Platform Trial): An Umbrella-Basket Platform Trial to Evaluate the Efficacy of Targeted Therapies in Rare Adult, Paediatric and Teenage/Young Adult (TYA) Cancers With Actionable Genomic Alterations, Including Common Cancers With Rare Actionable Alterations. Treatment Arm 06: Capmatinib in Adult Patients With Cancers Harbouring MET Dysregulations

Cancer Research UK·interventional·Posted May 23, 2025·Updated Nov 24, 2025

In Brief

A Phase 3 clinical trial evaluating Capmatinib for Solid Tumour and 10 related conditions. Currently recruiting, targeting 30 participants across 17 sites.

Detailed Summary

This clinical trial is looking at a drug called capmatinib. Capmatinib is approved as standard of care treatment for adult patients with certain types of lung cancer. This means it has gone through clinical trials and been approved by the Medicines and Healthcare products Regulatory Agency (MHRA) in the UK. Capmatinib works in patients with lung cancer with a particular mutation in their cancer known as a METex14 skipping mutation. Investigators now wish to find out if it will be useful in treating patients with other cancer types which have the same mutation or other specific mutations or changes which take place in the MET gene. If the results are positive, the study team will work with the NHS and the Cancer Drugs Fund to see if these drugs can be routinely accessed for patients in the future. This trial is part of a trial programme called DETERMINE. The programme will also look at other anti-cancer drugs in the same way, through matching the drug to rare cancer types or ones with specific mutations.

Study Details

Timeline

Phase 3Recruiting
20252026202720282029
First PostedMay 23, 2025
Enrollment StartNov 19, 2024
Primary CompletionOct 1, 2029
TodayJul 1, 2026
Enrollment to primary: 4.9 yearsPosted 1.1 years agoPrimary completion in 3.3 years

Interventions

Capmatinibdrug

Patients will be administered capmatinib orally at a daily dose of 800 mg consisting of 400 mg (two 200mg tablets) twice daily. Each cycle of treatment will consist of 28 days and patients may continue on treatment until disease progression without clinical benefit, unacceptable AEs or withdrawal of consent.