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Precision Cancer Therapy in Rare Cancers

The MATRIX Clinical Studies of Precision Cancer Therapy for Rare Cancers

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06119789
Acronym
MATRIX-Rare
Enrollment
96
Registered
2023-11-07
Start date
2025-03-20
Completion date
2036-08-01
Last updated
2025-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rare Malignant Neoplasm

Brief summary

Some rare cancers are hard-to-treat and patients have a poor prognosis. It is known that some of these patients have targetable molecular alterations, and some benefit from targeted drugs. However in many cases these drugs are not approved for the rare cancers. In this study the aim is to do advanced molecular diagnostics to identify possible targets for therapy, and to treat accordingly.

Detailed description

All patients will have the tumour cells diagnosed with a large genepanel, analyzing more than 500 genes on DNA / RNA level. Patients will be treated based on the molecular characteristics of the tumor cells.

Interventions

DRUGImatinib

imatinib treatment based on molecular alterations

DRUGTrametinib

According to biomarkers

DRUGDabrafenib

According to biomarkers

Sponsors

Helse Stavanger HF
CollaboratorOTHER_GOV
University Hospital of North Norway
CollaboratorOTHER
StOlavs Hospital
CollaboratorUNKNOWN
Nordlandssykehuset HF
CollaboratorOTHER
Helse Nord-Trøndelag HF
CollaboratorOTHER
Sorlandet Hospital HF
CollaboratorOTHER_GOV
Møre og Romsdal Hospital Trust
CollaboratorOTHER
The Hospital of Vestfold
CollaboratorOTHER
Helse Fonna
CollaboratorOTHER
Haukeland University Hospital
CollaboratorOTHER
Sykehuset Ostfold
CollaboratorOTHER
Helse Forde
CollaboratorOTHER
Sykehuset Innlandet HF
CollaboratorOTHER
Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

simon two stage model

Eligibility

Sex/Gender
ALL
Age
16 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* ECOG 0-2, * identified biomarker, * reasonable biochemistry

Exclusion criteria

* ECOG 3-5 * serious other diseases

Design outcomes

Primary

MeasureTime frameDescription
Radiological response evaluation at 16 weeks of treatment16 weeksStandard radiological response evaluation, like RECIST criteria.

Secondary

MeasureTime frameDescription
Molecular analyses predicting responses2 yearsSequencing of tumor material and blood samples

Countries

Norway

Contacts

Primary ContactÅslaug Helland, MD PhD
ahelland@medisin.uio.no+4795940863
Backup ContactKathinka Slørdahl, MD PhD
katslo@ous-hf.no

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026