Multiple Myeloma Clinical Trial
This is:
- A prospective, randomized, open, phase II, multi-centre, interventional study. Patients
who are in at least PR and have received lenalidomide as 2nd line treatment for MM will
be recruited.
- The patients will be randomized into two groups. Group R will receive lenalidomide 25
mg/day p.o. continuously for 21 days and group Rb will receive a similar dose of
lenalidomide with the addition of 40 mg of dexamethasone p.o. on days 1, 8, 15 and 22
of every 28 day treatment cycle. Study includes a maximum of 24 cycles including two
consolidating cycles per patients.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
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|
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|
Phase 1/Phase 2 | |
| Withdrawn |
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|
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| Recruiting |
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