Summary
The primary purpose of the phase 1 part of the study is to evaluate safety and tolerability
of AMG 701 monotherapy to identify the RP2D for AMG 701 monotherapy followed by a
dose-confirmation part to gather further safety data for AMG 701 monotherapy at the RP2D in
adult subjects with relapsed/refractory multiple myeloma (RRMM). In addition, this study will
include a sequential dose exploration part to identify the RP2D of AMG 701 in combination
with pomalidomide, with and without dexamethasone (AMG 701-P+/-d). Phase 2 will consist of
the dose-expansion part to gain further efficacy and safety experience with AMG 701
monotherapy in adult subjects with RRMM.