Recruiting

Multiple Myeloma Patient Registry in Germany

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Blood Protein Disorders+12

+ Cardiovascular Diseases

+ Hematologic Diseases

Over 18 Years
+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Other

Utilizing specific methods not covered by standard models in order to address unique research questions.
Observational
Study Start: December 2022
See protocol details

Summary

Principal SponsorProf. Dr. Hartmut Goldschmidt
Study ContactEileen Kurre
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: December 8, 2022

Actual date on which the first participant was enrolled.

This study is a comprehensive registry focused on multiple myeloma, a type of blood cancer, in Germany. It is organized by the German-speaking Myeloma Multicenter Group (GMMG) and gathers data from patients across 35 centers. The registry aims to collect information about patients' diagnoses, treatments, and long-term outcomes to improve understanding of multiple myeloma. It includes data from both past and ongoing studies, such as a trial that evaluated the effectiveness of adding a specific antibody, elotuzumab, to standard therapy for those eligible for a stem cell transplant. By analyzing this information, the registry seeks to enhance treatment strategies and improve survival rates for patients. Participants in the registry are monitored throughout their treatment until they pass away, lose contact, or decide to leave the study. Information about their health is collected every six months, and after the first signs of disease progression, it is updated annually. The study looks at important factors like how long patients live without the cancer worsening and overall survival rates. Data is managed confidentially using a secured system, with regular checks to ensure accuracy. The registry does not involve any new treatments or interventions, focusing solely on observing and recording patients' experiences with the standard care they receive.

Official TitleNational, Observational, Non-interventional, Retro- and Prospective Clinical Multiple Myeloma Registry GMMG
NCT07111884
Principal SponsorProf. Dr. Hartmut Goldschmidt
Study ContactEileen Kurre
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

999 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other

Some studies use unique or mixed approaches that don't fit standard categories. These may include innovative observational methods or studies tailored to specific research questions.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Blood Protein DisordersCardiovascular DiseasesHematologic DiseasesHemic and Lymphatic DiseasesHemorrhagic DisordersImmune System DiseasesImmunoproliferative DisordersLymphoproliferative DisordersMultiple MyelomaNeoplasmsNeoplasms by Histologic TypeParaproteinemiasVascular DiseasesHemostatic DisordersNeoplasms, Plasma Cell

Criteria

1 inclusion criteria required to participate
Previous participation in a a therapy study of the GMMG study group

1 exclusion criteria prevent from participating
patients with organ amyloidosis at time of diagnosis

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 35 locations

Recruiting

HELIOS Klinikum, Klinik für Hämatologie, Onkologie und Immunologie

Berlin, GermanyOpen HELIOS Klinikum, Klinik für Hämatologie, Onkologie und Immunologie in Google Maps
Recruiting

Charité Campus Benjamin Franklin, III. Med. Abt. (Hämatologie/Onkologie)

Berlin, Germany
Recruiting

Klinikum Bielefeld, Klinik für Hämatologie, Onkologie und Palliativmedizin

Bielefeld, Germany
Recruiting

Medizinische Universitätsklinik, Knappschaftskrankenhaus

Bochum, Germany
Recruiting
35 Study Centers