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Clinical Trial Summary

The treatment with oral melphalan and prednisone has been recommended as standard treatment of AL amyloidosis but the results are rather disappointing. Another therapeutic option is pulsed high-dose dexamethasone + melphalan (Mel-Dex) with more encouraging results regarding the achievement of a faster disease response and higher rates of haematological remission. In the last 5 - 10 years, promising treatment outcomes after therapy with high-dose melphalan and autologous stem cell support have been reported by several groups but only highly selected patients are eligible for this treatment. Lenalidomide has been shown to be effective in phase II and III trials in MM patients. Because of the relationship to MM, Lenalidomide is a promising therapeutic option also for patients with AL amyloidosis. The addition of Lenalidomide to Mel-Dex could improve rate of complete response (CR) and organ response in patients not eligible for or refused high-dose chemotherapy.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00883623
Study type Interventional
Source Heidelberg University
Contact
Status Completed
Phase Phase 2
Start date April 2009
Completion date February 2013

See also
  Status Clinical Trial Phase
Completed NCT00651937 - Trial of Two Stem Cell Doses To Reduce Transplant Induced Symptom Burden Phase 2
Completed NCT00807872 - Radioimmunoimaging of AL Amyloidosis Phase 1
Completed NCT02555969 - Minimal Residual Disease as a Possible Predictive Factor for Relapse in Patients With AL Amyloidosis
Completed NCT01707264 - Phase 1/2, Open Label, Dose Escalation Study of NEOD001 in Subjects With Light Chain (AL) Amyloidosis Phase 1/Phase 2