US2023255993A1PendingUtilityA1
Treatment of triple negative breast cancer
Assignee: PARADOX PHARMACEUTICALS INCPriority: Mar 2, 2020Filed: Apr 21, 2023Published: Aug 17, 2023
Est. expiryMar 2, 2040(~13.6 yrs left)· nominal 20-yr term from priority
A61K 31/704A61K 47/14A61P 35/00A61K 47/02A61K 47/10A61K 9/0019
49
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present invention relates to compositions comprising at least one of pivarubicin and benzarubicin, or a pharmaceutically acceptable salt thereof, and methods for using the compositions in the treatment of triple negative breast cancer (TNBC) by administering an effective amount of the compositions to a subject. In some instances, the subject is a mammal, including at least one of human, feline, and canine mammals.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A method for treating triple negative breast cancer (TNBC), said method comprising administering to a subject an effective amount of at least one of pivarubicin and benzarubicin, or a pharmaceutically acceptable salt thereof.
2 . The method of claim 1 , wherein said subject is a mammal.
3 . The method of claim 1 , wherein treating TNBC further comprises inhibiting tumor growth.
4 . A composition comprising at least one of pivarubicin and benzarubicin, or a pharmaceutically acceptable salt thereof, and further comprising a nonionic surfactant.
5 . The composition of claim 4 , wherein said nonionic surfactant comprises polyethyleneglycol (15)-hydroxystearate.
6 . The composition of claim 5 , wherein said composition further comprises an alcohol.
7 . The composition of claim 4 , wherein the nonionic surfactant is present in an amount of about 0.1% to 1.0%.
8 . The composition of claim 4 , wherein the pivarubicin is present in an amount of about 0.5-3.0 mg/mL.
9 . The composition of claim 4 , wherein the pivarubicin is present in an amount of about 1 mg/mL.
10 . The composition of claim 4 , wherein the benzarubicin is present in an amount of about 0.5-3.0 mg/mL.
11 . The composition of claim 4 , wherein the benzarubicin is present in an amount of about 1 mg/mL.
12 . The composition of claim 4 , wherein the pivarubicin is present in an amount of about 0.5-3.0 mg/mL, and wherein the benzarubicin is present in an amount of about 0.5-3.0 mg/mL.
13 . The composition of claim 4 , wherein said composition is formulated for parenteral administration.
14 . A method for treating triple negative breast cancer (TNBC), said method comprising administering to a subject an effective amount of the composition according to claim 4 .
15 . The method of claim 12 , wherein said effective amount is about 0.5-3.0 mg/mL.
16 . The method of claim 12 , wherein the pivarubicin is present in an amount of about 300-750 mg cumulative dose.
17 . The method of claim 12 , wherein the benzarubicin is present in an amount of about 300-750 mg cumulative dose.
18 . The method of claim 12 , wherein the at least one of pivarubicin and benzarubicin is provided in a composition comprising 10% to 30% ethanol and 70% to 90% sterile saline.
19 . The method of claim 16 , wherein the nonionic surfactant in the composition according to claim 4 comprises polyethyleneglycol (15)-hydroxystearate.
20 . The method of claim 12 , wherein the at least one of pivarubicin and benzarubicin is provided in a composition comprising about 20% ethanol and about 80% sterile saline, and further comprising about 0.125% polyethyleneglycol (15)-hydroxystearate.Join the waitlist — get patent alerts
Track US2023255993A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.