Overview

TKI258 in Subjects With Refractory or Relapsed Multiple Myeloma

Status:
Terminated
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
The primary objective of this study is to determine the maximum tolerated dose (MTD), dose limiting toxicity (DLT), and safety profile of CHIR-258 when administered to subjects with refractory or relapsed multiple myeloma (MM).
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Novartis
Criteria
Inclusion Criteria:

- Confirmed diagnosis of multiple myeloma

- Evidence of relapsed or refractory disease

Exclusion Criteria:

- Intracranial disease or epidural disease

- Clinically significant cardiac disease

- Diabetes mellitus