The present invention relates to a pharmaceutical combination product for cancer therapy. The combination product comprises the two active ingredients glutaminase and 6-diazo-5-oxo-L-norleucine (DON). The invention further relates to the use of such a combination product for the treatment of cancers.
1. A combination product for cancer treatment, which combination product comprises the active ingredients
a) glutaminase and
b) 6-diazo-5-oxo-L-norleucine (DON),
where active ingredient a) is present in a dosage of from 40 I.U./m 2 to 300 I.U./m 2 based on a recipient; and
where active ingredient b) is present in a dosage of from 105 to 185 mg/m 2 based on a recipient, where in the glutaminase is a glutaminase asparaginase from Pseudomonas 7A.
2. The combination product as claimed in claim 1 , characterized in that active ingredient a) is modified and/or provided with one or more protective substances.
3. The combination product as claimed in claim 1 , characterized in that active ingredient a) is present in a concentration of from 50 I.U./m 2 to 200 I.U./m 2 (international units per body surface area of recipient), based on a recipient, in the combination product.
4. The combination product as claimed in claim 1 , characterized in that active ingredient a) is intended for administration three times a week to once every four weeks.
5. The combination product as claimed in claim 1 , characterized in that active ingredient b) is intended for administration four times a week to once every two weeks.
6. The combination product as claimed in claim 1 , characterized in that active ingredients a) and b) are present in a conjoint administration unit.
7. The combination product as claimed in claim 6 , characterized in that active ingredients a) and b) are present in two separate administration units
A) comprising active ingredient a) and
B) comprising active ingredient b).
8. The combination product as claimed in claim 7 , characterized in that at least one administration unit is in injectable form.
9. The combination product as claimed in claim 7 , characterized in that at least one administration unit is in intravenous form.
10. The combination product as claimed in claim 7 , characterized in that at least one administration unit is in oral form.