Connect® MM- The Multiple Myeloma Disease Registry
Stopped: Business objectives have changed
United States3,011 participantsStarted 2009-09-01
Plain-language summary
The purpose of the Connect® MM Registry is to explore the natural history and real world management of patients with newly diagnosed symptomatic multiple myeloma (MM) and provide unique insights into the management of MM and the impact of this hematologic disorder on patients.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
Cohort 1 and 2
* Newly diagnosed with symptomatic MM within 2 months of enrollment in Connect® MM registry
* Age ≥18 years
* Willing and able to provide signed informed consent
* Agrees to complete patient assessment questionnaires either alone or with minimal assistance from caregivers and/or trained site personnel
Cohort 3
* Received 1L therapy for symptomatic active MM and subsequently has evidence of disease progression. Prior 1L MM treatment received, including anti-myeloma therapy, transplant, chemotherapy, radiation, and surgery, must be known.
* Initiated or intends to initiate 2L systemic therapy for MM after the first documented relapsed/refractory date (i.e. 1L PD).
* Enrollment date must be within 90 days of start date (or intended start date) of 2L systemic therapy.
Exclusion Criteria:
Cohort 1 and 2
\- None
Cohort 3
* Patient's 1L MM treatment was for smoldering MM or MGUS, and not for symptomatic MM
* Currently active in any MM Registry, including but not limited to, the Connect® MM registry or another Celgene/BMS-Sponsored registry.
* Patients who have discontinued from Connect® MM or another Celgene/BMS-Sponsored registry could be considered for enrollment in Cohort 3, if inclusion and exclusion criteria are met.
* Currently enrolled or intending to enroll within 90 days in any interventional clinical trial in which any treatment is an investigational product that cannot be identified
What they're measuring
1
Participant baseline demographics
Timeframe: Baseline
2
Participant medical history
Timeframe: Baseline
3
Participant Multiple Myeloma diagnosis information
Timeframe: Baseline
4
Participant Multiple Myeloma treatment history
Timeframe: Baseline
5
Multiple Myeloma-related supportive concomitant medications and procedures
Timeframe: Baseline, every 3-months up to 5 years (Cohort 3), or up to 16 years (Cohort 1 & 2), or date of early discontinuation
6
Occurance of second primary malignancy
Timeframe: Baseline, every 3-months up to 5 years (Cohort 3), or up to 16 years (Cohort 1 & 2), or date of early discontinuation
7
Number of participants enrolled in a clinical trial
Timeframe: Baseline, every 3-months up to 16 years or date of early discontinuation