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A Study Evaluating the Safety and Pharmacokinetics of ABBV-744 in Participants With Relapsed/Refractory Acute Myeloid Leukemia (AML) Cancer
This is an open-label, Phase 1, dose-escalation (Segment 1) and expansion (Segment 2) study to determine the maximum tolerated dose (MTD) and/or the recommended phase two dose (RPTD), and to assess the safety, preliminary efficacy, and pharmacokinetic (PK) profile of ABBV-744 in participants with relapsed/refractory Acute Myeloid Leukemia (AML).
Details
| Lead sponsor | AbbVie |
|---|---|
| Phase | PHASE1 |
| Status | TERMINATED |
| Enrolment | 30 |
| Start date | Fri Mar 16 2018 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Sat Dec 19 2020 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Acute Myeloid Leukemia (AML)
Interventions
- ABBV-744
Countries
United States