Claims for Patent: 10,441,645

Summary for Patent: 10,441,645

Title:	MSLN targeting DNA vaccine for cancer immunotherapy
Abstract:	The present invention relates to an attenuated mutant strain of Salmonella comprising a recombinant DNA molecule encoding Mesothelin. In particular, the present invention relates to the use of said attenuated mutant strain of Salmonella in cancer immunotherapy.
Inventor(s):	Springer; Marco (Wendlingen, DE), Lubenau; Heinz (Neustadt an der Weinstrasse, DE)
Assignee:	VAXIMM GMBH (DE)
Application Number:	15/785,743
Patent Claims:	1. A method for treating or vaccinating a patient against a cancer comprising administering to the patient an attenuated mutant strain of Salmonella comprising at least one copy of a recombinant DNA molecule comprising an expression cassette encoding Mesothelin (MSLN), wherein the MSLN is human MSLN, the attenuated mutant strain of Salmonella is Salmonella typhi Ty21a, and wherein the expression cassette is a eukaryotic expression cassette. 2. The method of claim 1, wherein the recombinant DNA molecule further comprises the kanamycin antibiotic resistance gene, the pMB1 ori, and wherein the eukaryotic expression cassette encoding human MSLN is under the control of a CMV promoter, wherein the human MSLN has the nucleic acid sequence as found in SEQ ID NO:2. 3. The method of claim 1, wherein the method further comprises administration of one or more further strain(s) of Salmonella comprising at least one copy of a recombinant DNA molecule comprising an expression cassette encoding a tumor antigen and/or a tumor stroma antigen, and wherein the one or more further strain(s) of Salmonella is/are Salmonella typhi Ty21a comprising a eukaryotic expression cassette. 4. The method of claim 3, wherein the one or more further strain(s) of Salmonella typhi Ty21a of claim 3, is co-administered with the attenuated mutant strain of Salmonella typhi Ty21a. 5. The method of claim 1, wherein the method further comprises administering chemotherapy, radiotherapy or a checkpoint inhibitory antibody to the patient. 6. The method of claim 1, wherein the attenuated mutant strain of Salmonella typhi Ty21a is administered orally. 7. The method of claim 1, wherein the cancer is selected from mesotheliomas, ovarian and pancreatic cancers, squamous cell carcinomas of the cervix, head and neck, vulva, lung and esophagus, lung adenocarcinomas, endometrial carcinomas, biphasic synovial sarcomas, desmoplastic small round cell tumors, and gastric adenocarcinomas. 8. The method of claim 1, wherein the single dose comprises from about 10.sup.5 to about 10.sup.11, particularly from about 10.sup.6 to about 10.sup.10, more particularly from about 10.sup.6 to about 10.sup.9, more particularly from about 10.sup.6 to about 10.sup.8, most particularly from about 10.sup.6 to about 10' colony forming units (CFU) of said attenuated mutant strain of Salmonella typhi Ty21a. 9. The method of claim 1 further comprising the step of assessing the MSLN expression pattern and/or the pre-immune response against MSLN of the patient, and wherein the treatment is individualized cancer immunotherapy treatment. 10. The method of claim 1, wherein MSLN has the amino acid sequence of SEQ ID NO:1 or is at least 80% identical to SEQ ID NO:1. 11. The method of claim 3, wherein said one or more further strain(s) of Salmonella typhi Ty21a comprise(s) a strain of Salmonella typhi Ty21 encoding human VEGFR-2. 12. The method of claim 5, wherein the attenuated mutant strain of Salmonella typhi Ty21a is administered before or during the chemotherapy or the radiotherapy treatment, or before or during administration of the checkpoint inhibitory antibody or before and during the chemotherapy or the radiotherapy treatment or administration of the checkpoint inhibitory antibody.

Details for Patent 10,441,645

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Bavarian Nordic A/s	VIVOTIF	typhoid vaccine live oral ty21a	Capsule	103123	December 15, 1989		2033-12-18