PHARMACEUTICAL COMPOSITION COMPRISING ANTIEMETIC COMPOUNDS AND POLYORTHOESTER
The present disclosure provides for sustained release pharmaceutical formulations which can deliver both a 5-hydroxytryptamine 3 (5HT3) receptor antagonist and a neurokinin-1 (NK1) receptor antagonist to a subject in need thereof. Formulations described herein are suitable for subcutaneous administration. Also described are methods of treatment of various disorders, including chemotherapy-induced nausea and vomiting (CINV). The disclosed compositions and methods provide for less frequent dosing of the therapeutic agents, thereby increasing subject comfort and compliance.
1 . A pharmaceutical composition comprising a 5-HT3 receptor antagonist or a pharmaceutically acceptable salt thereof, a NK-1 receptor antagonist or a pharmaceutically acceptable salt thereof and a polyorthoester.
2 . The pharmaceutical composition of claim 1 , comprising about 10-50 weight percent of a polyorthoester-compatible liquid excipient and about 1-5 weight percent granisetron, the polyorthester comprising subunits selected from:
where
x is an integer selected from 1, 2, 3, and 4,
the total amount of p is an integer selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 and 20,
s is an integer selected from 1, 2, 3, and 4,
the mole percentage of α-hydroxyacid containing subunits in the polyorthoester is from about 0.1 to about 25 mole percent,
and the polyorthoester has a molecular weight in a range of about 1000 to 10,000.
3 . The composition of claim 1 , wherein the 5-HT3 receptor antagonist is granisetron or ondansetron.
4 . The composition of claim 1 , wherein the NK-1 receptor antagonist is aprepitant or fosaprepitant.
5 . The composition of claim 1 , wherein the 5-HT3 receptor antagonist is granisetron and the NK-1 receptor antagonist is aprepitant or fosaprepitant.
6 . The composition of claim 1 , wherein the 5-HT3 receptor antagonist is ondansetron and the NK-1 receptor antagonist is aprepitant or fosaprepitant.
7 . The composition of claim 1 , wherein the pharmaceutical composition is formulated for subcutaneous administration.
8 . A method of treating a subject suffering from chemotherapy-induced nausea and vomiting comprising subcutaneously administering to the subject a pharmaceutical composition comprising a 5-HT3 receptor antagonist or a pharmaceutically acceptable salt thereof, a NK-1 receptor antagonist or a pharmaceutically acceptable salt thereof and a polyorthoester.
9 . The method of claim 8 , wherein the 5-HT3 receptor antagonist is granisetron or ondansetron and the NK-1 receptor antagonist is aprepitant or fosaprepitant.
10 . The method of claim 8 , wherein the composition comprises about 10-50 weight percent of a polyorthoester-compatible liquid excipient and about 1-5 weight percent of the 5-HT3 receptor antagonist or a pharmaceutically acceptable salt thereof, the polyorthester comprising subunits selected from:
where
x is an integer selected from 1, 2, 3, and 4,
the total amount of p is an integer selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 and 20,
s is an integer selected from 1, 2, 3, and 4,
the mole percentage of α-hydroxyacid containing subunits in the polyorthoester is from about 0.1 to about 25 mole percent,
and the polyorthoester has a molecular weight in a range of about 1000 to 10,000.
11 . A method of treating a subject suffering from chemotherapy-induced nausea and vomiting comprising, a first pharmaceutical composition comprising a 5-HT3 receptor antagonist or a pharmaceutically acceptable salt thereof and a polyorthoester, and a second pharmaceutical composition comprising a NK-1 receptor antagonist or a pharmaceutically acceptable salt thereof and a polyorthoester.
12 . A subcutaneous dosage form comprising aprepitant or a pharmaceutically acceptable salt thereof and a polyorthoester, wherein the polyorthester comprises subunits selected from:
where
x is an integer selected from 1, 2, 3, and 4,
the total amount of p is an integer selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 and 20,
s is an integer selected from 1, 2, 3, and 4,
the mole percentage of α-hydroxyacid containing subunits in the polyorthoester is from about 0.1 to about 25 mole percent,
and wherein the polyorthoester has a molecular weight in a range of about 1000 to 10,000.
13 . A subcutaneous dosage form comprising fosaprepitant or a pharmaceutically acceptable salt thereof and a polyorthoester, wherein the polyorthester comprises subunits selected from:
where
x is an integer selected from 1, 2, 3, and 4,
the total amount of p is an integer selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 and 20,
s is an integer selected from 1, 2, 3, and 4,
the mole percentage of α-hydroxyacid containing subunits in the polyorthoester is from about 0.1 to about 25 mole percent,
and wherein the polyorthoester has a molecular weight in a range of about 1000 to 10,000.