Oral forms of a phosphonic acid derivative
Novel solution complexes of zoledronic acid are described which give rise to improved properties of zoledronic acid. The invention includes aqueous solution and molecular complexes of zoledronic acid with and optical isomers of asparagine, histidine, arginine and proline as well as pharmaceutical complexes containing them and methods of treatment using them.
1. A pharmaceutical formulation comprising:
about 1% to about 99% by weight of a solution complex of zoledronic acid and a coformer selected from the group consisting of asparagine, histidine, arginine and proline; and
about 99% to about 1% by weight of a pharmaceutical excipient.
2. A pharmaceutical formulation of claim 1 , wherein the amino acid is selected from the group consisting of L-asparagine, DL-asparagine, L-histidine, DL-histidine, L-arginine, DL-arginine, L-proline, and DL-proline.
3. A pharmaceutical formulation of claim 2 , wherein the complex is:
a solution complex of zoledronic acid and L-histidine having an aqueous solubility of zoledronic acid to greater than 350 mg/ml,
a solution complex of zoledronic acid and DL-histidine having an aqueous solubility of zoledronic acid to greater than 350 mg/ml,
a solution complex of zoledronic acid and L-arginine having an aqueous solubility of zoledronic acid to greater than 235 mg/ml,
a solution complex of zoledronic acid and DL-arginine having an aqueous solubility of zoledronic acid to greater than 235 mg/ml,
a solution complex of zoledronic acid and L-asparagine having an aqueous solubility of zoledronic acid to greater than 50 mg/ml, or
a solution complex of zoledronic acid and DL-asparagine having an aqueous solubility of zoledronic acid to greater than 50 mg/ml.
4. A pharmaceutical formulation of claim 1 , wherein the formulation is an oral dosage form.
5. A pharmaceutical formulation of claim 4 , wherein the formulation is a solution, a suspension, or solution in capsule of the solution complex.
6. A method for the treatment of disease states associated with osteoporosis, tumor induced hypercalcemia (TIH), or Paget's disease comprising the step of administering to a patient in need thereof a therapeutically effective amount of a pharmaceutical formulation of claim 1 .
7. A method for the treatment of disease states associated with osteoporosis, tumor induced hypercalcemia (TIH), or Paget's disease comprising the step of administering to a patient in need thereof a therapeutically effective amount of a pharmaceutical formulation of claim 4 .
8. A method for the treatment of disease states associated with osteoporosis, tumor induced hypercalcemia (TIH), or Paget's disease comprising the step of administering to a patient in need thereof a therapeutically effective amount of a pharmaceutical formulation of claim 5 .
9. A method of claim 6 , wherein the pharmaceutical formulation is administered orally or parenterally.