Manufacture of Degarelix
The present invention provides methods for producing a lyophilized degarelix product which, upon reconstitution with water for injection in an amount of 20 mg/ml, shows a viscosity of up to 15 mPas. The present invention also provides a lyophilized degarelix drug substance which shows, upon dissolution in water in an amount of 20 mg/ml, a viscosity of up to 3.2 mPas, and processes for providing this lyophilized degarelix drug substance.
1. A method for producing a degarelix drug substance comprising:
a. purifying degarelix obtained by solid phase peptide synthesis to obtain a degarelix solution with a purity of at least 95%, as determined by high-performance liquid chromatography (HPLC);
b. concentrating the degarelix solution to obtain aggregated degarelix;
c. deaggregating the aggregated degarelix with acetic acid to obtain deaggregated degarelix; and
d. lyophilizing the deaggregated degarelix to provide the degarelix drug substance.
2. The method of claim 1 , wherein concentrating the degarelix solution involves evaporating from the degarelix solution solvent.
3. The method of claim 1 , wherein the purity of the degarelix solution is at least 97.5%.
4. The method of claim 1 , wherein the deaggregated degarelix has an acetic acid concentration of 15 to 35% (v/v).
5. The method of claim 1 , wherein the deaggregated degarelix has a temperature of minus 5 (−5) to 30 degrees centigrade.
6. The method of claim 1 , wherein the deaggregated degarelix has a free base concentration of 10 to 35 g/l.
7. A method for producing a degarelix drug substance comprising:
a. purifying degarelix to obtain a degarelix solution with a purity of at least 95%, as determined by high-performance liquid chromatography (HPLC);
b. loading the degarelix solution onto a chromatographic column;
c. eluting degarelix from the column to provide eluted degarelix;
d. lyophilizing the eluted degarelix to provide the degarelix drug substance.
8. The method of claim 7 , wherein the eluted degarelix is filtered prior to lyophilization.
9. The method of claim 7 , wherein the purity of the degarelix solution is at least 97.5%.
10. The method of claim 7 , wherein the degarelix is deaggregated with acetic acid to form a deaggregated degarelix drug substance.
11. The method of claim 10 , wherein the deaggregated degarelix has an acetic acid concentration of 15 to 35% (v/v).
12. The method of claim 10 , wherein the deaggregated degarelix has a temperature of minus 5 (−5) to 30 degrees Centigrade.
13. The method of claim 7 , wherein the deaggregated degarelix has a free base concentration of 10 to 35 WI.
14. A method for producing a degarelix drug substance comprising:
a. purifying degarelix to obtain a degarelix solution with a purity of at least 95%, as determined by high-performance liquid chromatography (HPLC);
b. adjusting an acetic acid concentration of the purified degarelix solution to 6 to 40% (w/w); and
c. spray-drying the degarelix solution to provide the degarelix drug substance.