Multiple Myeloma Clinical Trial
Official title:
Phase II Clinical Trial of Oral Suberoylanilide Hydroxamic Acid (SAHA) in Patients With Advanced Multiple Myeloma
The purposes of this study are:
- To determine the maximum tolerated dose (MTD) of SAHA administered every 12 hours for 14
consecutive days followed by 7 days of rest during the first two cycles (i.e., first 6
weeks) in patients with advanced multiple myeloma;
- To assess the safety and overall response rate to SAHA in patients with advanced
multiple myeloma.
n/a
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