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  <body><![CDATA[<p><strong>&quot;Chimeric Antigen Receptor T Cells: Clinical Development, FDA Approval, and What&rsquo;s Coming Next&quot;</strong></p>

<p><strong>Bruce Levine, Ph.D.<br />
Barbara and Edward Netter Professor in Cancer Gene Therapy<br />
University of Pennsylvania Perelman School of Medicine</strong></p>

<p>Since the 1990&rsquo;s, we have conducted clinical trials of gene modified T cells. Chimeric antigen receptor (CAR) T cells targeting CD19 on B cells leukemias and lymphomas have induced durable complete responses in patients who are relapsed or refractory to all other available treatments.&nbsp;</p>

<p>This synthetic biology technology has now undergone global multi-center clinical trials and recently received FDA approval (Kymriah<sup>TM</sup>, Novartis) in relapsed/refractory acute lymphoid leukemia in children and young adults.&nbsp;CAR T cells targeting new targets in hematologic malignancies and in solid tumors are underway and provide demonstration that it is possible to design immunity at will for therapeutic application.&nbsp;&nbsp;</p>
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