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Clinical Trials/NCT03308474
NCT03308474
Recruiting
N/A

Clinical Research Platform for Molecular Testing, Treatment and Outcome of Patients With Multiple Myeloma (Myeloma Registry Platform; MYRIAM)

iOMEDICO AG1 site in 1 country2,200 target enrollmentSeptember 25, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Multiple Myeloma
Sponsor
iOMEDICO AG
Enrollment
2200
Locations
1
Primary Endpoint
Course of treatment (treatment reality)
Status
Recruiting
Last Updated
3 months ago

Overview

Brief Summary

The purpose of the project is to set up a national, prospective, longitudinal, multicenter cohort study with associated satellites, a tumor registry platform, to document uniform data on characteristics, molecular diagnostics, treatment and course of disease, to collect patient-reported outcomes and to establish a decentralized biobank for patients with Multiple Myeloma in Germany.

Detailed Description

MYRIAM is a national, observational, prospective, longitudinal, multicenter cohort study (tumor registry platform) with the purpose to record information on the antineoplastic treatment of multiple myeloma in Germany. The registry will follow patients for up to five years. It will identify common therapeutic sequences and changes in the treatment of the disease. At inclusion, data in patient characteristics, comorbidities, tumor characteristics and previous treatments are collected. During the course of observation data on all systemic treatments, radiotherapies, surgeries, and outcome are documented. Health-realted quality of life in patients with multiple myeloma (MyLife) will be evaluated for up to five years.

Registry
clinicaltrials.gov
Start Date
September 25, 2017
End Date
December 1, 2028
Last Updated
3 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • MM requiring systemic (first-, second- or third-line) treatment (closed for first-line / second-line recruitment)
  • Age ≥ 18 years
  • Written informed consent
  • Patients participating in the PRO satellite: signing of informed consent and completion of baseline questionnaire before, but not more than eight weeks before the start of respective systemic treatment
  • Patients not participating in the PRO satellite: signing of informed consent not later than four weeks after start of respective treatment, and not more than eight weeks before the start of respective systemic treatment
  • Sufficient German language skills for participation in the PRO satellite

Exclusion Criteria

  • No systemic therapy for myeloma
  • Patients already enrolled in studies that prohibit any participation in other studies

Outcomes

Primary Outcomes

Course of treatment (treatment reality)

Time Frame: 5 years per patient

Documentation of anamnestic data and therapy sequences

Secondary Outcomes

  • Health-related quality of life (Patient-reported outcome)(5 years per patient)
  • Best Response(5 years per patient)
  • Progression-free survival(5 years per patient)
  • Myeloma-specific health-related quality of life (Patient-reported outcome)(5 years per patient)
  • Quality of life (Patient-reported outcome)(5 years per patient)
  • Overall survival(5 years per patient)

Study Sites (1)

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