IP Library Granted Patent US 11,925,676
Granted Patent B2
US 11,925,676 · App. 18/175,112 · Granted Mar 12, 2024

Method for treating neoplasia with an anti-CD38 antibody and an IL-15:IL-15R complex

Inventors: Bai Liu (Culver City, CA); Peter Rhode (Culver City, CA); Wenxin Xu (Culver City, CA); Hing C. Wong (Culver City, CA)
Assignee: Altor Bioscience, LLC.
A61K38/2086A61K38/1793A61K39/39558A61K47/6425A61P35/00A61K39/04C07K14/35C07K14/5443C07K14/7155C07K16/2818C07K16/2827C07K16/2887C07K16/2896C07K16/32C07K2317/732C07K2319/30C07K2319/32
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Quick Facts
Patent No.
US 11,925,676
App. No.
18/175,112
Granted
Mar 12, 2024
Kind
B2
Abstract

The invention features combination therapies using an IL-15-based superagonist complex and an antibody to effectively treat subjects with cancer and infectious diseases.

Claims (23)

1. A method for treating a neoplasia. in a subject, the method comprising: administering to said subject an effective amount of an isolated anti-CD38 antibody and an effective amount of a pharmaceutical composition comprising an IL-15:IL-15RαSu complex, wherein the effective amount of the IL-15:IL-15RαSu complex is between 0.1 μg/kg and 100 mg/kg, thereby treating the neoplasia.

2. The method of claim 1 , wherein the IL-15:IL-15RαSu complex comprises a wild type IL-15 molecule.

3. The method of claim 1 , wherein the IL-15:IL-15RαSu complex comprises an IL-15 molecule having the amino acid sequence of SEQ ID NO:3.

4. The method of claim 1 , wherein the IL-15:IL-15RαSu complex comprises an IL-15RαSuFc fusion construct having the amino acid sequence of SEQ NO:6.

5. The method of claim 1 , wherein the IL-15:IL-15RαSu complex is Alt-803.

6. The method of claim 1 , wherein the subject is suffering from a neoplasia and the neoplasia is selected from the group consisting of a glioblastoma, prostate cancer, hematological cancer, B-cell neoplasms, multiple myeloma, B-cell lymphoma, Hodgkin's lymphoma, chronic lymphocytic leukemia, acute myeloid leukemia, cutaneous T-cell lymphoma, T-cell lymphoma, a solid tumor, urothelial carcinoma, bladder carcinoma, melanoma, lung cancer, renal cell carcinoma, breast cancer, gastric cancer, esophageal cancer, head and neck cancer, colorectal cancer, ovarian cancer, non-small cell lung carcinoma, B-Cell non-Hodgkin's lymphoma, and squamous cell head and neck carcinoma.

7. The method of claim 6 , wherein the subject is suffering from multiple myeloma.

8. The method of claim 1 , wherein the effective amount of the IL-15:IL-15RαSu complex is administered daily.

9. The method of claim 1 , wherein the effective amount of the IL-15:IL-15RαSu complex is administered once or twice per week.

10. The method of claim 1 , wherein the effective amount of the IL-15:IL-15RαSu complex is between 0.1 μg/kg and 1 mg/kg.

11. The method of claim 1 , wherein the pharmaceutical composition is administered by subcutaneous, intravenous, intraperitoneal, intramuscular, or intradermal injection, or by intravesicular instillation.

12. The method of claim 1 , wherein the anti-CD38 antibody is daratumumab.

13. The method of claim 1 , wherein antibody-dependent mediated cytotoxicity (ADCC) or antibody-dependent cellular phagocytosis (ADCP) mediated by said antibody against tumor cells in said subject is augmented by at least 5% following said administration.

14. The method of claim 1 , wherein said antibody and the IL-15:IL-15RαSu complex increase levels of blood NK cell, T cell, neutrophil or monocyte counts or activity.

15. The method of claim 1 , wherein said antibody and the IL-15:IL-15RαSu complex stimulate CD4+ or CD8+ T cells to kill tumor cells.

16. The method of claim 1 , wherein said antibody and the IL-15:IL-15RαSu complex stimulate NK cells to kill tumor cells.

17. The method of claim 1 , wherein said antibody and the IL-15:IL-15RαSu complex stimulate neutrophils or monocytic cells to kill tumor cells.

18. The method of claim 1 , wherein said administration results in a decrease in the number of tumor cells.

19. The method of claim 1 , wherein said administration results in a decrease in disease progression of the neoplasia.

20. The method of claim 1 , wherein said administration results in prolonged survival of said subject compared to untreated subjects.

21. The method of claim 1 , wherein said subject is a human.

22. The method of claim 1 , wherein said antibody and the IL-15:IL-15RαSu complex increase blood cytokine levels.

23. The method of claim 22 , wherein said cytokine comprises IFN-γ and/or IL-6.

Assignments (3)
SECURITY INTEREST Recorded Jan 2, 2024
From: IMMUNITYBIO, INC.; NANTCELL, INC.; RECEPTOME, INC.; VBC HOLDINGS LLC; ALTOR BIOSCIENCE, LLC; ETUBICS CORPORATION; IGDRASOL, INC.
To: INFINITY SA LLC, AS PURCHASER AGENT
Reel/Frame 066179/0074 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2023
From: LIU, BAI; RHODE, PETER; XU, WENXIN; WONG, HING C.
To: ALTOR BIOSCIENCE CORPORATION
Reel/Frame 063303/0352 →
MERGER Recorded Apr 12, 2023
From: ALTOR BIOSCIENCE CORPORATION
To: ALTOR BIOSCIENCE, LLC
Reel/Frame 063303/0489 →
Continuity (8)
Continuation 18063871 · Dec 9, 2022
Division 17825959 · May 26, 2022
Continuation 16925138 · Jul 9, 2020
Continuation 16444807 · Jun 18, 2019
Continuation 15921512 · Mar 14, 2018
Division 14755989 · Jun 30, 2015
Provisional Application 62018899 · Jun 30, 2014
Related Publication 20230233649A1 · Jul 27, 2023
Cited By (3)
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