The Norwegian Immunotherapy in Multiple Myeloma Study
- Sponsor
- St. Olavs Hospital
- Study ID
- NCT06855121
- Status
- Recruiting
Conditions
- AL Amyloidosis
- Myeloma Multiple
- Plasma Cell Leukemia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Teclistamab — DRUGReal-world use and dosing
- Elranatamab — DRUGReal-world use and dosing
- Ciltacabtagene Autoleucel — BIOLOGICALReal-world use.
- Talquetamab — DRUGReal-world use and dosing
- Idecabtagene vicleucel — BIOLOGICALReal-world use and dosing
Study Details
The goal of this observational study is to study the effectiveness and complications of novel immunotherapies used in the treatment of multiple myeloma in routine care in Norway. The aim is to close knowledge gaps, generate evidence for future clinical trials and contribute to future consensus on how to monitor for adverse events, and what mitigation strategies should be implemented, so that we can increase patient survival and quality-of-life.
Key Dates
- Start date
- Jan 15, 2025
- Status verified
- Feb 2025
- Primary completion
- Jan 31, 2029
- Completion
- Dec 1, 2037
Study Design
- Enrollment
- 400 participants (estimated)
Primary Outcome Measure
Determine the real-world overall response rates (ORR) [ Time Frame: From date of treatment start and until date of first documented progression or start of next line of therapy, whichever came first, assessed up to ten years. ]
Central Contacts
- Tobias S Slørdahl, MD PhD+4772825100
- Juni S Paulsen, MD+4772825100
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