METHODS OF TREATING UREA CYCLE DISORDERS
The present disclosure provides novel methods for determining an effective dosage of a PAA prodrug and for treating a UCD that incorporate body surface area and urinary PAGN concentration. The disclosure further provides novel methods for assessing compliance with PAA prodrug administration that incorporate urinary PAGN concentration, and the subject's current dosing regimen, BSA, or age. The disclosure further provides novel methods of treating a UCD in a subject in need thereof that incorporate urinary PAGN concentration, and the subject's current dosing regimen, BSA, and/or age.
1 - 20 . (canceled)
21 . A method of treating a urea cycle disorder (UCD) in a subject in need thereof who is less than two years of age comprising:
a) administering glyceryl tri-[4-phenylbutyrate] to the subject whose urinary PAGN level is above 9000 μg/ml at the previously administered dosage, or
b) administering an adjusted dosage of the glyceryl tri-[4-phenylbutyrate] to the subject whose urinary PAGN level is below 9000 μg/ml.
22 . The method of claim 21 , wherein the dosage of glyceryl tri-[4-phenylbutyrate] is administered orally.
23 . The method of claim 21 , wherein the effective dosage is 5 to 12.4 g/m 2 /day.
24 . The method of claim 23 , wherein the effective dosage is at or about 7 to 9.5 g/m 2 /day, 7.5 to 9 g/m 2 /day, 8.0 to 8.5 g/m 2 /day, or 8.3 to 8.5 g/m 2 /day.
25 . The method of claim 24 , wherein the effective dosage is at or about 8.02 or 8.35 g/m 2 /day.
26 . The method of claim 21 , wherein the subject has not previously been administered one or more dosages of glyceryl tri-[4-phenylbutyrate].
27 . The method of claim 21 , wherein the subject in need thereof lacks systemic control of endogenous blood ammonia levels.
28 . A method of assessing compliance in a subject suffering from a urea cycle disorder (UCD) who is less than two years of age comprising:
a) testing urinary PAGN level of the subject; and
b) administering glyceryl tri-[4-phenylbutyrate] to the subject whose urinary PAGN level is above 9000 μg/ml at the previously administered dosage, or
c) administering an adjusted dosage of the glyceryl tri-[4-phenylbutyrate] to the subject whose urinary PAGN level is below 9000 μg/ml.