IP Library Granted Patent US 9,328,156
Granted Patent B2
US 9,328,156 · App. 14/107,302 · Granted May 3, 2016

Use of chimeric antigen receptor-modified T cells to treat cancer

Inventors: Carl H. June (Merion Station, PA); Bruce L. Levine (Cherry Hill, NJ); David L. Porter (Springfield, PA); Michael D. Kalos (Philadelphia, PA); Michael C. Milone (Cherry Hill, NJ)
Assignee: The Trustees of the University of Pennsylvania
C07K14/70578A61K35/17A61K39/0011A61K39/39558C07K14/70517C07K14/70596C07K16/2896C12N5/0636C12N15/85A61K2039/505A61K2039/5156A61K2039/5158C07K2317/80C12N2501/515C12N2510/00
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Quick Facts
Patent No.
US 9,328,156
App. No.
14/107,302
Granted
May 3, 2016
Kind
B2
Abstract

The present invention provides compositions and methods for treating cancer in a human. The invention includes relates to administering a genetically modified T cell to express a CAR wherein the CAR comprises an antigen binding domain, a transmembrane domain, a costimulatory signaling region, and a CD3 zeta signaling domain.

Claims (15)

1. A pharmaceutical composition comprising an anti-tumor effective amount of a population of human T cells, wherein the T cells comprise a nucleic acid sequence that encodes a chimeric antigen receptor (CAR), wherein the CAR comprises a CD19 antigen binding domain, a transmembrane domain, a 4-1BB costimulatory signaling region, and a CD3 zeta signaling domain comprising the amino acid sequence of SEQ ID NO: 24, wherein the T cells are of a human having cancer.

2. The composition of claim 1 , wherein the anti-tumor effective amount of T cells is 10 4 to 10 9 cells per kg body weight of a human in need of such cells.

3. The composition of claim 2 , wherein the anti-tumor effective amount of T cells is 10 5 to 10 6 cells per kg body weight of a human in need of such cells.

4. The composition of claim 1 , wherein the CD19 antigen binding domain is an antibody or an antigen-binding fragment thereof.

5. The composition of claim 4 , wherein the antigen binding fragment is a Fab or scFv.

6. The composition of claim 5 , wherein the antigen binding fragment is an scFv.

7. The composition of claim 6 , wherein the scFv comprises the amino acid sequence of SEQ ID NO: 20.

8. The composition of claim 1 , wherein the transmembrane domain is CD8α transmembrane domain.

9. The composition of claim 8 , wherein the CD8α transmembrane domain comprises the amino acid sequence of SEQ ID NO: 22.

10. The composition of claim 1 , wherein the CAR further comprises a hinge domain.

11. The composition of claim 1 , wherein the 4-1BB costimulatory signaling region comprises the amino acid sequence of SEQ ID NO: 23.

12. The composition of claim 6 , wherein the scFv is encoded by a nucleic acid sequence comprising SEQ ID NO: 14.

13. The composition of claim 8 , wherein the CD8α transmembrane domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 16.

14. The composition of claim 1 , wherein the 4-1BB costimulatory signaling region is encoded by a nucleic acid sequence comprising SEQ ID NO: 17.

15. The composition of claim 1 , wherein the CD3 zeta signaling domain is encoded by a nucleic acid sequence comprising SEQ ID NO: 18.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 3, 2024
From: JUNE, CARL H.; LEVINE, BRUCE L.; PORTER, DAVID L.; KALOS, MICHAEL D.; MILONE, MICHAEL C.
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 067599/0455 →
CONFIRMATORY LICENSE Recorded Mar 17, 2015
From: UNIVERSITY OF PENNSYLVANIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 035218/0777 →
Continuity (4)
Continuation 13992622
Provisional Application 61502649 · Jun 29, 2011
Provisional Application 61421470 · Dec 9, 2010
Related Publication 20140106449A1 · Apr 17, 2014