Myeloma Registry Platform (MYRIAM)
Clinical Research Platform for Molecular Testing, Treatment and Outcome of Patients With Multiple Myeloma (Myeloma Registry Platform; MYRIAM)
iOMEDICO AG
2,200 participants
Sep 25, 2017
OBSERVATIONAL
Conditions
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.
Eligibility
Inclusion Criteria6
- 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 Criteria2
- No systemic therapy for myeloma
- Patients already enrolled in studies that prohibit any participation in other studies
Interventions
Physician's choice according to patient's needs.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT03308474