drugset / Trial / NCT02152956

Flotetuzumab in Primary Induction Failure (PIF) or Early Relapse (ER) Acute Myeloid Leukemia (AML)

NCT02152956 ↗

Phase 1/2 Terminated 244 enrolled MacroGenics
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Open-label, multi-dose, single-arm, multi-center, Phase 1/2 study conducted in three segments: the Single Patient Dose Escalation Segment (complete), followed by the Multi-Patient Dose Escalation Segment (complete) and the Maximum Tolerated Dose and Schedule (MTDS) Expansion Cohort Segment (closed). Having characterized safety and determined the maximum tolerated dose and schedule, the primary objective of this study now is to assess the anti-neoplastic activity of flotetuzumab in patients with PIF/ER AML, as determined by the proportion of patients who achieve CR or CRh. Starting with Cycle 2, patients who are benefiting from flotetuzumab may receive up to a maximum of 8 cycles of treatment. Patients will receive daily increasing doses of flotetuzumab for the first week of Cycle 1 (Lead-In Dosing) followed by 3 weeks of continuous intravenous infusion at a the assigned dose. Subsequent cycles are each 4 weeks of continuous infusion at the assigned dose. Dosing may continue for up to 8 cycles. Follow up visits may continue for 6 months after treatment is discontinued.

Timeline

Start
2014-06-09
Primary completion
2022-07-05
Completion
2022-07-05

Outcome

Outcome not reported

Stopped (Business): “Business decision”

Drugs

EvaluationDrugModalityDoseRoute
Subject Flotetuzumab Monoclonal antibody 3 ng —
Subject Flotetuzumab Monoclonal antibody 10 ng —
Subject Flotetuzumab Monoclonal antibody 30 ng —
Subject Flotetuzumab Monoclonal antibody 100 ng —
Subject Flotetuzumab Monoclonal antibody 300 ng —
Subject Flotetuzumab Monoclonal antibody 500 ng —
Subject Flotetuzumab Monoclonal antibody 700 ng —
Subject Ruxolitinib Small molecule — Oral