Intravenous infusion dosage form
The present invention relates to an intravenous infusion dosage form of pemetrexed or its pharmaceutically acceptable salt, having long term stability.
1. An intravenous infusion dosage form comprising
a) a composition consisting essentially of pemetrexed or its pharmaceutically acceptable salt present at a concentration ranging from about 0.7 mg/ml to about 21 mg/ml, an osmogent and an inert gas in solution in a parenteral aqueous vehicle, the solution having a volume ranging from about 50 ml to 1000 ml,
b) a flexible infusion container containing the composition of (a) and an inert gas in a headspace of the infusion container,
c) a second container surrounding the flexible infusion container with an inert gas or vacuum in the space between the flexible infusion container and the second container,
wherein the total impurities are less than 2.0% by weight.
2. The intravenous infusion dosage form of claim 1 , wherein the dosage form is subjected to moist heat sterilization.
3. The intravenous infusion dosage form of claim 1 , wherein the second container is made up of aluminum.
4. The intravenous infusion dosage form of claim 1 , wherein the inert gas is selected from nitrogen, argon or helium.
5. The intravenous infusion dosage form of claim 1 , wherein the dosage form is prepared by a method comprising the steps of
a) dissolving pemetrexed or its pharmaceutically acceptable salt and an osmogent in a parenteral aqueous vehicle,
b) filling the solution of step (a) into a flexible infusion container,
c) sealing the filled flexible infusion container,
d) surrounding the flexible infusion container by a second container and sealing the second container,
e) subjecting the container of step (d) to moist heat sterilization,
wherein in each of the above steps, low oxygen conditions are maintained in the solution and/or in the head space of the flexible infusion container and in the space between the flexible infusion container and the second container.
6. The intravenous infusion dosage form of claim 5 , wherein the method further comprises maintaining the dosage form of step (d) for at least 12 hours prior to step (e).
7. The intravenous infusion dosage form of claim 5 , wherein the increase in total impurities of Pemetrexed during moist heat sterilization is less than 0.2%.
8. An intravenous infusion dosage form comprising:
a) a composition consisting essentially of pemetrexed or its pharmaceutically acceptable salt present at a concentration ranging from about 0.7 mg/ml to about 21 mg/ml, an osmogent and an inert gas in solution in a parenteral aqueous vehicle, the solution having a volume ranging from about 50 ml to 1000 ml,
b) a rigid infusion container containing the composition of (a) and an inert gas in a headspace of the infusion container,
wherein the dosage form is subjected to moist heat sterilization and wherein the total impurities are less than 2.0% by weight.
9. The intravenous infusion dosage form of claim 8 wherein the infusion container is surrounded by a second container, with an inert gas or vacuum in the space between the infusion container and the second container.