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Clinical Trials/NCT03409692
NCT03409692
Completed
Not Applicable

Validation of a Personalised Medicine Tool for Multiple Myeloma That Predicts Treatment Effectiveness in Patients

Mario Boccadoro1 site in 1 country278 target enrollmentJune 14, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Multiple Myeloma
Sponsor
Mario Boccadoro
Enrollment
278
Locations
1
Primary Endpoint
MMpredictor as a personalised medicine tool
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The consortium aims to commercialise the MMpredictor as a personalised medicine tool that predicts the most effective treatment strategy for individual Multiple Myeloma (MM) patients. MM is the second most common form of blood cancer contributing to 15% of all blood cancers and ~1,5% and 2% of all cancer deaths annually in the EU and US, respectively.

Patients show a large variability in treatment response and side effects due to tumour heterogeneity and the patient's intrinsic characteristics. Therefore, not every treatment will be suitable for each patient, and treatment strategies are often based on trial-and-error. The availability of multiple (>20) treatment options complicates treatment decision-making even more. With the current development of many more promising treatments, there is an urgent unmet clinical need for a diagnostic assay that supports personalised cancer treatment in order to improve patient health outcomes, prevent side effects and reduce healthcare costs.

SkylineDx has previously developed the MMprofiler, a microarray-based diagnostic test that can subtype MM patients and reliably predict MM patient survival (prognosis). In this project, the test's clinical value will be expanded to include the prediction of treatment effectiveness in individual patients based on Gene Expression Profiling. An addendum for new intended use will be filed to the current in vitro diagnostic (IVD) registration, while renaming the test to MMpredictor. The project will also focus on positioning the test as a cost-effective IVD test for personalised medicine, that will increase health outcome and quality of life of patients and reduce healthcare costs.

The consortium consists of a life science SME specialised in molecular diagnostics, clinical centres with world renowned KOLs, a leading health economic institute, and a European MM patient advocacy organisation combining all the required complementary expertise to successfully bring the MMpredictor to market.

Registry
clinicaltrials.gov
Start Date
June 14, 2017
End Date
July 25, 2022
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Mario Boccadoro
Responsible Party
Sponsor Investigator
Principal Investigator

Mario Boccadoro

Director of Department of Molecular Biotechnology and Health Sciences

University of Turin, Italy

Eligibility Criteria

Inclusion Criteria

  • The bio-banked MM patient samples and clinical data will be obtained from previous European clinical trials that have been conducted over the past 5 years within the participating clinical centres and other clinical centers. The samples were not collected for the purposes of this project. The subjects from which the data was initially taken cannot be identified from the data/records. However, the patients from the above mentioned trial have explicitly consented for the use of their samples for other (future) clinical research purposes.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

MMpredictor as a personalised medicine tool

Time Frame: 1 year

The main objective of the MMpredict project is to commercialise the MMpredictor as a personalised medicine tool that predicts the most effective treatment strategy for individual Multiple Myeloma (MM) patients.

Secondary Outcomes

  • - Clinical validation of genetic subtypes correlating with specific treatment effect(2 years)
  • - Perform a Medical Technology Assessment (MTA) to evaluate health economic benefits(2 years)
  • - Establish a treatment decision matrix that will guide physicians in treatment decision-making(2 years)
  • - Develop and execute commercialisation and marketing plan for the MMpredictor(2 years)
  • - Genetic subtyping with the MMprofiler of 800 bio-banked MM patient samples(2 years)
  • - File addendum to current CE-IVD registration, while also renaming the test to "MMpredictor"(2 years)

Study Sites (1)

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