abstract |
A process for preparing a sealed vial or cartridge containing a ready for parenteral administration liquid pharmaceutical formulation, comprising: (a) combining human parathyroid hormone, a buffer to maintain a pH from greater than 3 to about 7, and a stabilizer, thereby forming a solution, and (b) sealing the vial or cartridge containing said solution, from which a therapeutically effective dose of parathyroid hormone can be withdrawn for use by a patient. פירוט זה נבחן בהתאם לתקנה 35 לתקנות הפטנטים, תשכ" ח-1968 This specification was examined in accordance with regulation 35 of the Patent Regulations, 5728-1968. |