Intravenous infusion dosage form
The present invention refers to an intravenous infusion dosage form comprising a composition containing pemetrexed or its pharmaceutically acceptable salt, an osmagent and an aquous vehicle. The composition is present in a flexible infusion container containing an inert gas in the headspace. Additionally, a second container may be present surrounding the flexible infusion container.
1. An intravenous infusion dosage form comprising:
a) an aqueous composition comprising about 0.7 mg/ml to about 21 mg/ml of pemetrexed or its pharmaceutically acceptable salt, and an osmogent; and
b) a flexible infusion container containing the aqueous composition in a volume ranging from about 50 ml to about 1000 ml:
wherein the dosage form has less than 0.5% by weight of individual impurity B or impurity C after storage at 15-30° C. for at least 12 months, and
the aqueous composition is free of antioxidants.
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 container comprises a headspace, wherein the headspace is optionally occupied with an inert gas.
4. The intravenous infusion dosage form of claim 1 , wherein the dosage form comprises a second container surrounding the flexible infusion container, and the dosage form has a space between the second container and the flexible infusion container.
5. The intravenous infusion dosage form of claim 4 , wherein the second container is a flexible container or a solid container.
6. The intravenous infusion dosage form of claim 4 , wherein the space between the two containers optionally has an inert gas or oxygen scavenger.
7. The intravenous infusion dosage form of claim 1 , wherein the level of total impurities is less than 2.0% by weight after storage at 15-30° C. for at least 12 months.
8. The intravenous infusion dosage form of claim 1 , wherein the oxygen content in the dosage form is maintained below 2 ppm for at least 12 months.
9. The intravenous infusion dosage form of claim 8 , wherein the oxygen content is maintained by inert gas purging and/or filling.
10. The intravenous infusion dosage form of claim 4 , wherein the second container is made of aluminum.
11. The intravenous infusion dosage of claim 6 , wherein the inert gas is selected from nitrogen, argon and helium.
12. A method of treating cancer in a patient in need thereof, the method comprising administering an intravenous infusion dosage form to the patient, wherein the intravenous infusion dosage comprises:
a) an aqueous composition comprising about 0.7 mg/ml to about 21 mg/ml of pemetrexed or its pharmaceutically acceptable salt, and an osmogent; and
b) a flexible infusion container containing the composition in a volume ranging from about 50 ml to about 1000 ml;
wherein the dosage form has less than 0.5% by weight of individual impurity B or impurity C after storage at 15-30° C. for at least 12 months, and
the aqueous composition is free of antioxidants.
13. The method of claim 12 , wherein the cancer is selected from lung cancer, breast cancer, cervical cancer, colorectal cancer, cutaneous squamous cell carcinoma, endometrial carcinoma, esophageal cancer, gastric cancer, head and neck cancer, squamous cell cancer, hepatocellular carcinoma, Hodgkin lymphoma, malignant pleural mesothelioma, melanoma, Merkel cell carcinoma, microsatellite instability-high or mismatch repair-deficient cancer (unresectable or metastatic), non-small cell lung cancer, primary mediastinal large B-cell lymphoma, renal cell carcinoma, small cell lung cancer, and urothelial carcinoma.
14. The method of claim 13 , wherein the lung cancer is small cell or non-small cell lung cancer.
15. An intravenous infusion dosage form comprising:
a) an aqueous composition consisting essentially of about 0.7 mg/ml to about 21 mg/ml of pemetrexed or its pharmaceutically acceptable salt, and an osmogent; and
b) a flexible infusion container containing the aqueous composition in a volume ranging from about 50 ml to about 1000 ml:
wherein the dosage form has less than 0.5% by weight of individual impurity B or impurity C after storage at 15-30° C. for at least 12 months.
16. The intravenous infusion dosage form of claim 1 , wherein the dosage form is a ready to use infusion dosage form.