IP Library Granted Patent US 11,844,798
Granted Patent B2
US 11,844,798 · App. 17/130,387 · Granted Dec 19, 2023

Procaspase combination therapy for glioblastoma

Inventors: Paul J. Hergenrother (Champaign, IL); Rachel C. Botham (Champaign, IL); Timothy M. Fan (Mahomet, IL); Mark J. Gilbert (Seattle, WA); Michael K. Handley (Windsor, CO); Avadhut Joshi (Towson, MD); Gregory J. Riggins (White Hall, MD); Theodore M. Tarasow (San Ramon, CA)
Assignees: The Board of Trustees of the University of Illinois; Vanquish Oncology, Inc.; The Johns Hopkins University
A61K31/495A61K9/008A61K9/0019A61K9/2018A61K9/2054A61K9/4858A61K31/4188A61K31/53A61K47/10
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Quick Facts
Patent No.
US 11,844,798
App. No.
17/130,387
Granted
Dec 19, 2023
Kind
B2
Abstract

The invention provides compositions and methods for the induction of cell death, for example, cancer cell death. Combinations of compounds and related methods of use are disclosed, including the use of compounds in therapy for the treatment of cancer and selective induction of apoptosis in cells. The disclosed drug combinations can have lower neurotoxicity effects than other compounds and combinations of compounds.

Claims (7)

1. A method of treating a bone cancer in a subject in need thereof comprising administering to a subject, concurrently or sequentially, a therapeutically effective amount of each of the compounds temozolomide (TMZ) and first procaspase activating compound (PAC-1)

wherein the bone cancer is osteosarcoma, the TMZ and PAC-1 form a synergistic anticancer combination that is about 20% to about 93% more effective than an additive anticancer effect of TMZ and PAC-1, and osteosarcoma is thereby treated.

2. The method of claim 1 wherein a therapeutically effective concentration of PAC-1 is about 5 μM to about 30 μM, or about 50 mg/kg.

3. The method of claim 2 wherein a therapeutically effective concentration of TMZ is about 250 μM to about 750 μM, or about 50 mg/kg.

4. The method of claim 1 wherein the synergistic anticancer combination is more effective than an additive anticancer effect of TMZ and PAC-1, by about 20.34%, about 26.95%, about 37.72%, about 39.3%, about 39.96%, about 41.06%, about 45.3%, about 55.68%, about 62.57%, about 65.65%, about 69.3%, about 75.36%, about 79.42%, or about 93.49%.

5. The method of claim 1 wherein TMZ and PAC-1 are administered orally, intravenously, or a combination thereof.

6. The method of claim 1 wherein the synergistic anticancer combination is formed in vivo or in vitro.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2023
From: HERGENROTHER, PAUL J.; BOTHAM, RACHEL C.; FAN, TIMOTHY M.
To: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS
Reel/Frame 062530/0897 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2023
From: GILBERT, MARK J.; HANDLEY, MICHAEL K.; TARASOW, THEODORE M.
To: VANQUISH ONCOLOGY, INC.
Reel/Frame 062530/0915 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2023
From: JOSHI, AVADHUT; RIGGINS, GREGORY J.
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 062530/0953 →
Continuity (5)
Continuation 16148344 · Oct 1, 2018
Continuation 15243860 · Aug 22, 2016
Continuation 14383460
Provisional Application 61607103 · Mar 6, 2012
Related Publication 20210290616A1 · Sep 23, 2021