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



Status:Enrolling by invitation
Healthy:No
Age Range:Any
Updated:9/14/2018
Start Date:November 9, 2016
End Date:March 2040

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Long-term Follow-up Study of Patients Who Have Previously Been Exposed to UCART19 (Allogeneic Engineered T-cells Expressing a Lentiviral-based Anti-CD19 Chimeric Antigen Receptor)

The purpose of this study is to evaluate the long-term safety and efficacy of UCART 19
administration to patients with advanced lymphoid malignancies.


Inclusion Criteria:

- Written informed consent obtained prior any study-specific procedure (patient or
parent(s) or legal representative)

- Patient dosed with UCART19 who completed or discontinued early from a sponsored or
from any investigator-initiated study that tested UCART19, or patients who were
administered UCART19 under a special access scheme (compassionate use);

- Female patients of childbearing potential and male patients with partners of
childbearing potential must continue to use an effective method of birth control as
well as their partners.

Exclusion Criteria:

- No exclusion criteria for this study
We found this trial at
5
sites
1515 Holcombe Blvd
Houston, Texas 77030
 713-792-2121
University of Texas M.D. Anderson Cancer Center The mission of The University of Texas MD...
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Houston, TX
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4650 Sunset Blvd
Los Angeles, California 90027
 (323) 660-2450
Childrens Hospital Los Angeles Children's Hospital Los Angeles is a 501(c)(3) nonprofit hospital for pediatric...
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Los Angeles, CA
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3400 Spruce St
Philadelphia, Pennsylvania 19104
 (215) 662-4000
Hospital of the University of Pennsylvania The Hospital of the University of Pennsylvania (HUP) is...
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Philadelphia, PA
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Boston, Massachusetts 02114
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from
Boston, MA
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from
Gent,
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