Myeloma Registry Platform (MYRIAM)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsoriOMEDICO AG

About this trial

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 criteria

Qualifiers

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

Disqualifiers

No systemic therapy for myeloma

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

Trial design

Treatments tested in this trial

  • Routine care as per site standard.

Treatment groups

No treatment groups listed

Locations

1

Map coordinates are unavailable for these locations. Locations are shown below instead.

Multiple sites all over germanyRecruiting Multiple SitesGermanyGermany

Sponsors and collaborators

iOMEDICO AG

Lead sponsor

Deutsche Studiengruppe Multiples Myelom (DSMM)

Collaborator