drugset / Trial / NCT02978235

A Dose Finding Study Followed by a Safety and Efficacy Study for Patients With Multiple Myeloma or Lymphoma

NCT02978235 ↗

Phase 1 Terminated 11 enrolled Taiho Oncology, Inc.
NaSingle-groupOpen-labelTreatment

Summary

The Phase 1 portion of this study will determine the safety of TAS4464 and the most appropriate dose for patients with Multiple Myeloma or Lymphoma.

Timeline

Start
2017-03-01
Primary completion
2018-02-01
Completion
2018-02-01

Outcome

Outcome not reported

Stopped: “The trial was put on Clinical Hold and subsequently terminated prior to Phase 2 due to cases of drug induced liver injury meeting the criteria for Hy's Law”

Drugs

EvaluationDrugModalityDoseRoute
Subject TAS4464 Unknown — Intravenous