Sign in

NCT03308474Recruiting

Myeloma Registry Platform (MYRIAM)

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

Source: ClinicalTrials.gov · Last updated 13 Jul 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
2200 (estimated)
First submitted
25 Sept 2017
Start date
25 Sept 2017
Primary completion date
31 Dec 2026
Lead sponsor
iOMEDICO AG
NCT number
NCT03308474

What you commit to

  • Study type: Observational
  • Planned participants: 2200
  • From 25 Sept 2017 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • No systemic therapy for myeloma

Other

  • Patients already enrolled in studies that prohibit any participation in other studies

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Multiple sites all over germany
Coordinator of this site? Confirm its status
Multiple SitesGermanyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.