A Study to Evaluate the Safety and Tolerability of CAEL-101 in Patients With AL Amyloidosis
Completed · Phase 2
Conditions studied: AL Amyloidosis
In brief
AL amyloidosis begins in the bone marrow where abnormal proteins misfold and create free light chains that cannot be broken down. These free light chains bind together to form amyloid fibrils that build up in the extracellular space of organs, affecting the kidneys, heart, liver, spleen, nervous system and digestive tract. The primary purpose of this study is to determine the recommended dose of CAEL-101 to facilitate progression of further clinical trials and evaluate safety and tolerability of CAEL-101 in combination with the standard of care (SoC) cyclophosphamide-bortezomib-dexamethasone (CyBorD) chemotherapy and daratumumab .
Key facts
- Study ID
- NCT04304144
- Run by
- Alexion Pharmaceuticals, Inc.
- People needed
- 25
- Starts
- 2020-03-18
- Expected to finish
- 2023-11-14
- Last updated by the study team
- 2025-03-05
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Research Site — Stanford, California, United States
- Research Site — Detroit, Michigan, United States
- Research Site — Cleveland, Ohio, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.