Multi-arm polymer prodrugs
View Patent ↗Provided herein are water-soluble prodrugs, compositions comprising such prodrugs, and related methods of making and administering the same. The prodrugs of the invention comprise a water-soluble polymer having three or more arms, at least three of which are typically covalently attached to an active agent, e.g., a small molecule. The conjugates of the invention provide an optimal balance of polymer size and structure for achieving improved drug loading, since the conjugates of the invention possess three or more active agents releasably attached to a multi-armed water-soluble polymer. The prodrugs of the invention are therapeutically effective, and exhibit improved properties in-vivo when compared to unmodified parent drug.
1. A method of treating cancer in a mammalian subject, said method comprising:
administering a therapeutically effective amount of a composition comprising a prodrug having the structure:
or a pharmaceutically acceptable salt form thereof,
where n ranges from 40 to 500, to a subject having one or more cancerous solid tumors, over a duration of time effective to produce an inhibition of growth of said one or more cancerous solid tumors in said subject.
2. The method of claim 1 , wherein said cancerous solid tumor type is selected from the group consisting of colorectal, ovarian, breast, non-small cell lung and prostate.
3. The method of claim 2 , wherein the cancer is breast cancer.
4. The method of claim 2 , wherein the cancer is colorectal cancer.
5. The method of claim 2 , wherein the cancer is non-small cell lung cancer.
6. The method of claim 2 , wherein the cancer is prostate cancer.
7. The method of claim 2 , wherein the cancer is ovarian cancer.
8. The method of claim 1 , wherein the mammalian subject is human.
9. The method of claim 1 , wherein the overall nominal average molecular weight of the prodrug ranges from about 20,000 to about 80,000 daltons.
10. The method of claim 1 , wherein the composition further comprises one or more additional prodrugs having a structure selected from the group consisting of:
or a pharmaceutically acceptable salt form thereof,
wherein O-Irinotecan is
L is the site of attachment, and
n ranges from 40 to 500.
11. The method of claim 1 , wherein the composition further comprises a pharmaceutically acceptable carrier.
12. The method of claim 1 , wherein said administering is parenteral.
13. The method of claim 12 , wherein said parenteral administering is via a route selected from intraperitoneal, intravenous, subcutaneous, and intramuscular injection.
14. The method of claim 13 , wherein said administering is by intravenous infusion.
15. The method of claim 14 , wherein the composition comprises a sterile aqueous preparation of the prodrug.
16. The method of claim 7 , wherein the dosage administered comprises from about 10.0 to about 60 mg irinotecan/kg body weight of the subject.