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Active Org.- |
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Active Indication- |
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Drug Highest PhaseDiscontinued |
First Approval Ctry. / Loc.- |
First Approval Date20 Jan 1800 |
A Phase 1 Study of SGN-CD48A in Patients With Relapsed or Refractory Multiple Myeloma
This study will test the safety and activity of SGN-CD48A in patients with multiple myeloma. SGN-CD48A will be given on Days 1, 8, and 15 of a 28-day cycle. Prior to protocol amendment 2, SGN-CD48A was given every 3 weeks.
100 Clinical Results associated with SLAMF2 x Tubulin
100 Translational Medicine associated with SLAMF2 x Tubulin
0 Patents (Medical) associated with SLAMF2 x Tubulin