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A Phase 1/2a Open-label, Dose-escalation, Dose-expansion, Parallel Assignment Study to Evaluate the Safety and Clinical Activity of PBCAR0191 in Subjects with Relapsed/Refractory (r/r) Non-Hodgkin Lymphoma (NHL) and r/r B-cell Acute Lymphoblastic Leukemia

Clinical Trial Details

This clinical trial is for men and women who have Non-Hodgkin Lymphoma and B-Cell Acute Lymphoblastic Leukemia.
 
The purpose of this research is to gather information on the safety and effectiveness of PBCAR0191. PBCAR0191 is a new investigational treatment for certain types of blood cancers, such as leukemia and lymphoma, and is made from a type of blood cells known as T cells. 

Investigational means that PBCAR0191 has not yet been approved by the United States Food and Drug Administration (FDA).

The T cells in PBCAR0191 come from people who have donated their blood. The donated T cells have been genetically changed so that they may be able to kill some types of cancer cells. 
     
All participants will receive PBCAR0191 through an IV infusion at a dose determined by the study team. Participation in this research will last about 24 months.

Key Eligibility: 

-Men and women with a confirmed diagnosis of Non-Hodgkin Lymphoma or B-Cell Acute Lymphoblastic Leukemia        

Detailed eligibility will be reviewed when participants contact the study team.

Study contact by location

Upper East Side - Manhattan

Contact(s)

June Greenberg, RN
(212) 746-2651
jdg2002@med.cornell.edu

Primary Investigator(s)

Protocol ID(s)

Weill Cornell Medicine IRB #:

2005022153

ClinicalTrials.gov:

NCT03666000

Sponsor:

PBCAR0191-01

Status

Open to Enrollment

Age Group

Adult

Sponsor