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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03409692
Other study ID # Horizon2020 - FTI Pilot Study
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 14, 2017
Est. completion date July 25, 2022

Study information

Verified date June 2023
Source University of Turin, Italy
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 278
Est. completion date July 25, 2022
Est. primary completion date November 30, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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: -

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Gene Expression Profiling
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.

Locations

Country Name City State
Italy University of Turin Turin

Sponsors (1)

Lead Sponsor Collaborator
Mario Boccadoro

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary MMpredictor as a personalised medicine tool 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. 1 year
Secondary - Genetic subtyping with the MMprofiler of 800 bio-banked MM patient samples 2 years
Secondary - Clinical validation of genetic subtypes correlating with specific treatment effect 2 years
Secondary - Establish a treatment decision matrix that will guide physicians in treatment decision-making 2 years
Secondary - Perform a Medical Technology Assessment (MTA) to evaluate health economic benefits 2 years
Secondary - File addendum to current CE-IVD registration, while also renaming the test to "MMpredictor" 2 years
Secondary - Develop and execute commercialisation and marketing plan for the MMpredictor 2 years
See also
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Completed NCT02812706 - Isatuximab Single Agent Study in Japanese Relapsed AND Refractory Multiple Myeloma Patients Phase 1/Phase 2
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Active, not recruiting NCT03989414 - A Study to Determine the Recommended Dose and Regimen and to Evaluate the Safety and Preliminary Efficacy of CC-92480 in Combination With Standard Treatments in Participants With Relapsed or Refractory Multiple Myeloma (RRMM) and Newly Diagnosed Multiple Myeloma (NDMM) Phase 1/Phase 2
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Completed NCT02546167 - CART-BCMA Cells for Multiple Myeloma Phase 1