TY - JOUR
T1 - Ammonia control and neurocognitive outcome among urea cycle disorder patients treated with glycerol phenylbutyrate
AU - Diaz, George A.
AU - Krivitzky, Lauren S.
AU - Mokhtarani, Masoud
AU - Rhead, William
AU - Bartley, James
AU - Feigenbaum, Annette
AU - Longo, Nicola
AU - Berquist, William
AU - Berry, Susan A.
AU - Gallagher, Renata
AU - Lichter-Konecki, Uta
AU - Bartholomew, Dennis
AU - Harding, Cary O.
AU - Cederbaum, Stephen
AU - Mccandless, Shawn E.
AU - Smith, Wendy
AU - Vockley, Gerald
AU - Bart, Stephen A.
AU - Korson, Mark S.
AU - Kronn, David
AU - Zori, Roberto
AU - Merritt, J. Lawrence
AU - Nagamani, Sandesh C.S.
AU - Mauney, Joseph
AU - Lemons, Cynthia
AU - Dickinson, Klara
AU - Moors, Tristen L.
AU - Coakley, Dion F.
AU - Scharschmidt, Bruce F.
AU - Lee, Brendan
PY - 2013/6
Y1 - 2013/6
N2 - Glycerol phenylbutyrate is under development for treatment of urea cycle disorders (UCDs), rare inherited metabolic disorders manifested by hyperammonemia and neurological impairment. We report the results of a pivotal Phase 3, randomized, double-blind, crossover trial comparing ammonia control, assessed as 24-hour area under the curve (NH3-AUC0-24hr), and pharmacokinetics during treatment with glycerol phenylbutyrate versus sodium phenylbutyrate (NaPBA) in adult UCD patients and the combined results of four studies involving short- and long-term glycerol phenylbutyrate treatment of UCD patients ages 6 and above. Glycerol phenylbutyrate was noninferior to NaPBA with respect to ammonia control in the pivotal study, with mean (standard deviation, SD) NH3-AUC0-24hr of 866 (661) versus 977 (865) μmol·h/L for glycerol phenylbutyrate and NaPBA, respectively. Among 65 adult and pediatric patients completing three similarly designed short-term comparisons of glycerol phenylbutyrate versus NaPBA, NH3-AUC0-24hr was directionally lower on glycerol phenylbutyrate in each study, similar among all subgroups, and significantly lower (P < 0.05) in the pooled analysis, as was plasma glutamine. The 24-hour ammonia profiles were consistent with the slow-release behavior of glycerol phenylbutyrate and better overnight ammonia control. During 12 months of open-label glycerol phenylbutyrate treatment, average ammonia was normal in adult and pediatric patients and executive function among pediatric patients, including behavioral regulation, goal setting, planning, and self-monitoring, was significantly improved. Conclusion: Glycerol phenylbutyrate exhibits favorable pharmacokinetics and ammonia control relative to NaPBA in UCD patients, and long-term glycerol phenylbutyrate treatment in pediatric UCD patients was associated with improved executive function (ClinicalTrials.gov NCT00551200, NCT00947544, NCT00992459, NCT00947297).
AB - Glycerol phenylbutyrate is under development for treatment of urea cycle disorders (UCDs), rare inherited metabolic disorders manifested by hyperammonemia and neurological impairment. We report the results of a pivotal Phase 3, randomized, double-blind, crossover trial comparing ammonia control, assessed as 24-hour area under the curve (NH3-AUC0-24hr), and pharmacokinetics during treatment with glycerol phenylbutyrate versus sodium phenylbutyrate (NaPBA) in adult UCD patients and the combined results of four studies involving short- and long-term glycerol phenylbutyrate treatment of UCD patients ages 6 and above. Glycerol phenylbutyrate was noninferior to NaPBA with respect to ammonia control in the pivotal study, with mean (standard deviation, SD) NH3-AUC0-24hr of 866 (661) versus 977 (865) μmol·h/L for glycerol phenylbutyrate and NaPBA, respectively. Among 65 adult and pediatric patients completing three similarly designed short-term comparisons of glycerol phenylbutyrate versus NaPBA, NH3-AUC0-24hr was directionally lower on glycerol phenylbutyrate in each study, similar among all subgroups, and significantly lower (P < 0.05) in the pooled analysis, as was plasma glutamine. The 24-hour ammonia profiles were consistent with the slow-release behavior of glycerol phenylbutyrate and better overnight ammonia control. During 12 months of open-label glycerol phenylbutyrate treatment, average ammonia was normal in adult and pediatric patients and executive function among pediatric patients, including behavioral regulation, goal setting, planning, and self-monitoring, was significantly improved. Conclusion: Glycerol phenylbutyrate exhibits favorable pharmacokinetics and ammonia control relative to NaPBA in UCD patients, and long-term glycerol phenylbutyrate treatment in pediatric UCD patients was associated with improved executive function (ClinicalTrials.gov NCT00551200, NCT00947544, NCT00992459, NCT00947297).
UR - https://www.scopus.com/pages/publications/84879118512
UR - https://www.scopus.com/pages/publications/84879118512#tab=citedBy
U2 - 10.1002/hep.26058
DO - 10.1002/hep.26058
M3 - Article
C2 - 22961727
AN - SCOPUS:84879118512
SN - 0270-9139
VL - 57
SP - 2171
EP - 2179
JO - Hepatology
JF - Hepatology
IS - 6
ER -