Last updated: May 2, 2024
Sponsor: All4Cure
Overall Status: Active - Recruiting
Phase
N/A
Condition
Multiple Myeloma
Bone Diseases
Leukemia
Treatment
All4Cure Platform
Multiple Myeloma Pathway
Documentation Pathway
Clinical Study ID
NCT06149910
All4Cure03
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Diagnosis of multiple myeloma
- Diagnosis must occur on or after the formal launch of the MRD-targeted clinicalpathway in the Exigent network
- Diagnosis must be indicated by the presence of any of the following diagnosticcodes for multiple myeloma: [C90.00]
- Diagnosis must be confirmed on human review of the medical record
- Age ≥ 18 years at qualifying diagnosis.
- Patient has continued to receive care at a QCCA/Exigent Research practice for at least 90 days after the index date. Patients in the Documentation Cohort must meet the following additional inclusion criteria.
• Evidence in the record of a threshold level of adherence to the clinical pathway, orimplied intention to adhere to the clinical pathway. In addition to the inclusion criteria for the documentation cohort, patients in thePlatform Cohort must meet the following additional inclusion criteria.
- A record of registration by the patient for participation in the All4Cure platform,including signed HIPAA release forms that allow All4Cure to access their medicalrecords.
- A record of registration by the patient's primary treating physician for participationin the All4Cure platform.
Exclusion
Exclusion Criteria:
- Patients with a concurrent other malignancy (except basal cell carcinoma, squamouscell carcinoma of the skin, or in situ malignancies of breast or cervix), or those whohave received treatment of another malignancy within three years prior to diagnosis ofmultiple myeloma (except for treatment of basal cell carcinoma, squamous cellcarcinoma of the skin, or in situ malignancies of breast or cervix), are excluded fromeligibility.
- Patients with multiple myeloma subtypes Immunoglobulin D (IgD) or Immunoglobulin E (IgE) are excluded due to the very low rate of these subtypes.
- Patients who transfer their care to another facility outside the QCCA/Exigent Researchnetwork within the first 90 days after NDMM diagnosis are excluded.
Study Design
Total Participants: 450
Treatment Group(s): 3
Primary Treatment: All4Cure Platform
Phase:
Study Start date:
April 18, 2024
Estimated Completion Date:
December 01, 2026
Study Description
Connect with a study center
All4Cure
Seattle, Washington 98126
United StatesActive - Recruiting
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