A Study to Evaluate the Long-term Safety of Patients With Advanced Lymphoid Leukemia Who Have Been Previously Administered With UCART19

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

March 10, 2021

Primary Completion Date

September 30, 2028

Study Completion Date

September 30, 2028

Conditions
Advanced Lymphoid Leukemia
Interventions
BIOLOGICAL

UCART19 follow-up

UCART19 will not be administered during the study period. Patients who will be rolled-over from the parent study to this long term follow-up study, have previously received UCART19. The roll-over occurs at the end of the parent study, or at any time after UCART19 administration, in case of premature discontinuation from the parent study.

Trial Locations (16)

19104

Children's Hospital of Philadelphia, Philadelphia

33612

Moffit Cancer Center, Tampa

75010

Hôpital Saint-Louis, Paris

75019

Hôpital Robert-Debré, Paris

75235

University of Texas Southwestern Medical Center, Dallas

75571

Hôpital Saint-Antoine, Paris

77030

University of Texas MD Anderson Cancer Center, Houston

80219

Colorado Blood Cancer Institute, Denver

90027

Children's Hospital Los Angeles, Los Angeles

02129

Massachussetts General Hospital, Charlestown

812-8582

Kyushyu University Hospital, Fukuoka

060-8648

Hokkaido University Hospital, Sapporo

08950

Hospital San Juan De Dios, Barcelona

SE5 9RS

King's College Hospital NHS Foundation Trust, London

Unknown

UCL Great Ormond Hospital, London

M20 4BX

The Christie NHS Foundation Trust, Manchester

All Listed Sponsors
collaborator

ADIR, a Servier Group company

INDUSTRY

lead

Institut de Recherches Internationales Servier

OTHER