Pharmaceutical oxaliplatinum preparation for parenteral administration and method for obtaining same

1. A stable pharmaceutical preparation of oxaliplatin for parenteral administration, in which the oxaliplatin is in solution in a solvent at a concentration of at least 7 mg/ml, and wherein the solution of oxaliplatin has been subjected to an operation of wet heat treatment with steam in the saturation state and under pressure at a temperature not exceeding 110° C., and wherein the solvent of said solution which contains the oxaliplatin comprises a sufficient amount of at least one hydroxylated derivative chosen from 1,2-propanediol, glycerol, maltitol, sucrose and inositol.

2. The stable pharmaceutical preparation of oxaliplatin as claimed in claim 1 , characterized in that said solution has been subjected to an operation of wet heat treatment at a temperature of between 110° C. and about 70° C.

3. The stable pharmaceutical preparation of oxaliplatin as claimed in claim 1 , characterized in that said solution has been subjected to an operation of wet heat treatment at a temperature of about 80° C.

4. The stable pharmaceutical preparation of oxaliplatin as claimed in claim 1 , characterized in that said wet heat treatment operation is carried out in the course of at least two cycles composed of a phase of heating at said temperature and then a phase of returning to aid standing at ambient temperature.

5. The stable pharmaceutical preparation of oxaliplatin as claimed in claim 4 , characterized in that said phase of heating at the temperature lasts about 30 minutes and the phase of returning to and standing at ambient temperature lasts about 24 hours.

6. The stable pharmaceutical preparation of oxaliplatin as claimed in claim 1 , characterized in that said solvent also comprises water.

7. A method for obtaining a stable pharmaceutical preparation of oxaliplatin for parenteral administration, in which the oxaliplatin is in solution in a solvent at a concentration of at least 7 mg/ml, comprising dissolving oxaliplatin in a solvent comprising a sufficient amount of at least one hydroxylated derivative chosen from 1,2-propanediol, glycerol, maltitol, sucrose and inositol, and subjecting the solution to an operation of wet heat treatment with steam in the saturation state and under pressure at a temperature not exceeding 110° C.

8. The method as claimed in claim 7 , which also comprises, prior to said wet heat treatment operation, the implementation of the following steps:

a) bringing an amount of oxaliplatin into contact, at a temperature less than 80° C., with a sufficient amount of said solvent in order to obtain a concentration of oxaliplatin of at least 7 mg/ml; and

b) establishing the mixture obtained in step a) at a temperature of between 15° C. and 30° C.