Safety and Efficacy of Lacutamab in Patients With Relapsed/Refractory Peripheral T-cell Lymphoma That Express KIR3DL2

PHASE1CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

March 17, 2022

Primary Completion Date

November 19, 2023

Study Completion Date

February 8, 2024

Conditions
Peripheral T Cell Lymphoma
Interventions
BIOLOGICAL

lacutamab

Patients will receive a fixed dose of 750mg as 1-hour IV infusion

Trial Locations (20)

10065

Memorial Sloan Kettering Cancer Center- David H. Koch Center for Cancer Care, New York

15224

Allegheny Health, Pittsburgh

21201

University of Maryland, Baltimore

29425

Medical University of South Carolina - Health Hollings Cancer Center, Charleston

35015

Chungnam National University Hospital, Daejeon

35294

University of Alabama at Birmingham- O'Neal Comprehensive Cancer Center, Birmingham

46202

Indiana University School of Medicine, Indianapolis

46526

Goshen Health- Goshen Hospital, Goshen

52242

University of Iowa, Iowa City

77030

The University of Texas MD Anderson Cancer Center, Houston

92868

University of California at Irvine - Chao Family Comprehensive Cancer Center, Orange

Unknown

Inje University Busan Paik Hospital, Busan

Seoul National University Bundang Hospital, Gyeonggi-do

Gachon University Gil Medical Center, Incheon

Asan Medical Center, Seoul

Korea University Anam Hospital, Seoul

Samsung Medical Center, Seoul

Seoul National University Hospital, Seoul

Severance Hospital Yonsei University Health System, Seoul

07345

The Catholic University of Korea, Yeouido St. Mary's Hospital, Seoul

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Innate Pharma

INDUSTRY