drugset / Trial / NCT02556346

Pharmacokinetics (PK), Pharmacodynamics (PD), Safety, Tolerability of Multiple Dose Regimens of MT-3724 for the Treatment of Patients With Relapsed Chronic B-cell Lymphocytic Leukemia or Small Lymphocytic Lymphoma

NCT02556346 ↗

Phase 1 Withdrawn Molecular Templates, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This Phase I, multiple ascending dose study will seek to enroll subjects with relapsed/refractory Chronic B-cell Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL) with confirmed and measurable disease who have received standard treatment with at least one anti-CD20 antibody (e.g.; rituximab, ofatumumab) containing front-line regimen that resulted in initial response, followed by relapse/recurrence and who are not eligible for any further approved biologic therapy, chemotherapy and/or autologous stem transplantation and/or refuse alternative approved therapies and/or are unlikely to achieve clinical benefit from any therapy of higher priority by Investigator assessment.

Timeline

Start
2015-11
Primary completion
2016-08
Completion
2016-12

Outcome

Outcome not reported

Stopped: “The patient population (CLL \& SLL) was included in another ongoing study involving NHL patients.”

Drugs

EvaluationDrugModalityDoseRoute
Subject MT-3724 Unknown 5 ug/kg Intravenous
Subject MT-3724 Unknown 10 ug/kg Intravenous
Subject MT-3724 Unknown 20 ug/kg Intravenous
Subject MT-3724 Unknown 50 ug/kg Intravenous