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Clinical Trial Summary

This is a multicenter, randomized, open-label, parallel-group study to compare mLSG15 + KW-0761 to mLSG15 in subjects with CCR4-positive adult T-cell leukemia-lymphoma (untreated primary disease). The primary variable is an efficacy of KW-0761 used as an add-on therapy to mLSG15 as measured in terms of complete response rate (CR/CRu) in the best overall response assessment for antitumor effect. The secondary variables include response rate (CR/CRu/PR) in the best overall response assessment for antitumor effect, complete or response rates by lesion site in the best overall response assessment for antitumor effect, progression-free survival and overall survival. The safety and pharmacokinetic profiles of KW-0761 will be also determined.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01173887
Study type Interventional
Source Kyowa Hakko Kirin Co., Ltd
Contact
Status Completed
Phase Phase 2
Start date July 2010
Completion date April 2012

See also
  Status Clinical Trial Phase
Completed NCT01724177 - A Phase 2 Study of Lenalidomide in Patients With Relapsed or Recurrent Adult T-cell Leukemia-lymphoma Phase 2
Completed NCT01626664 - KW-0761 or Investigator's Choice in Subjects With Previously Treated Adult T-cell Leukemia-Lymphoma (ATL) Phase 2
Completed NCT00920790 - Phase II Study of KW-0761 in Subjects With CCR4-positive Adult T-cell Leukemia-lymphoma Phase 2
Completed NCT01169298 - A Phase I, Multicenter, Open-label, Dose-escalation Study to Assess the Safety of Lenalidomide in Patients With Advanced Adult T-cell Leukemia-lymphoma and Peripheral T-cell Lymphomaperipheral T-cell Lymphoma Phase 1
Recruiting NCT02737046 - Belinostat Therapy With Zidovudine for Adult T-Cell Leukemia-Lymphoma Phase 2