New hope for rare blood disease: teclistamab trial targets AL amyloidosis
NCT ID NCT06649695
First seen Jun 27, 2026 · Last updated Jul 21, 2026 · Updated 2 times
Summary
This study tests a drug called teclistamab in 30 people with AL amyloidosis, a rare disease where abnormal proteins damage organs. Participants have already had other treatments. The goal is to see if teclistamab can reduce or eliminate the harmful proteins in the blood. The study is currently recruiting.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CHU Limoges
Limoges, France
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Fondazione I.R.C.C.S Policlinico "San Matteo"
Pavia, Italy
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General Hospital of Athens "Alexandra"
Athens, Greece
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South Australia Health
Adelaide, Australia
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UMC Utrecht
Utrecht, Netherlands
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University Hospital Essen
Essen, Germany
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University Hospital Heidelberg
Heidelberg, Germany
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University Hospital Würzburg
Würzburg, Germany
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Westmead Hospital
Sydney, Australia
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a Dual-Targeting antibody stop amyloid buildup in its tracks?
- Can a radioactive peptide spot hidden amyloid in the heart?
- Real-world data on multiple myeloma immunotherapies could reshape monitoring and improve survival
- Nationwide registry aims to crack the code of a rare protein-clogging disease
- New scan spots hidden organ damage before symptoms start
- Could a simple scan unlock better heart treatment?