Evaluation of long-term effectiveness of the use of carglumic acid in patients with propionic acidemia (PA) or methylmalonic acidemia (MMA): study protocol for a randomized controlled trial

Marwan Nashabat, Abdulrahman Obaid, Fuad Al Mutairi, Mohammed Saleh, Mohammed Elamin, Hind Ahmed, Faroug Ababneh, Wafaa Eyaid, Abdulrahman Alswaid, Lina Alohali, Eissa Faqeih, Majed Aljeraisy, Mohamed A Hussein, Ali Alasmari, Majid Alfadhel, Marwan Nashabat, Abdulrahman Obaid, Fuad Al Mutairi, Mohammed Saleh, Mohammed Elamin, Hind Ahmed, Faroug Ababneh, Wafaa Eyaid, Abdulrahman Alswaid, Lina Alohali, Eissa Faqeih, Majed Aljeraisy, Mohamed A Hussein, Ali Alasmari, Majid Alfadhel

Abstract

Introduction: Propionic acidemia (PA) and methylmalonic acidemia (MMA) are rare autosomal recessive inborn errors of metabolism characterized by hyperammonemia due to N-acetylglutamate synthase (NAGS) dysfunction. Carglumic acid (Carbaglu®; Orphan Europe Ltd.) is approved by the US Food and Drug Administration (USFDA) for the treatment of hyperammonemia due hepatic NAGS deficiency. Here we report the rationale and design of a phase IIIb trial that is aimed at determining the long-term efficacy and safety of carglumic acid in the management of PA and MMA.

Methods: This prospective, multicenter, open-label, randomized, parallel group phase IIIb study will be conducted in Saudi Arabia. Patients with PA or MMA (≤15 years of age) will be randomized 1:1 to receive twice daily carglumic acid (50 mg/kg/day) plus standard therapy (protein-restricted diet, L-carnitine, and metronidazole) or standard therapy alone for a 2-year treatment period. The primary efficacy outcome is the number of emergency room visits due to hyperammonemia. Safety will be assessed throughout the study and during the 1 month follow-up period after the study.

Discussion: Current guidelines recommend conservative medical treatment as the main strategy for the management of PA and MMA. Although retrospective studies have suggested that long-term carglumic acid may be beneficial in the management of PA and MMA, current literature lacks evidence for this indication. This clinical trial will determine the long-term safety and efficacy of carglumic acid in the management of PA and MMA.

Trial registration: King Abdullah International Medical Research Center ( KAIMRC ): (RC13/116) 09/1/2014. Saudi Food and Drug Authority (SFDA) (33066) 08/14/2014. ClinicalTrials.gov (identifier: NCT02426775) 04/22/2015.

Keywords: Carbaglu®; Carglumic acid; Hyperammonemia; Methylmalonic acidemia; Propionic acidemia.

Conflict of interest statement

The clinical trial and the study medication are funded by Orphan Europe. The scientific design, data management, and data analysis are independent of the funding party.

Figures

Fig. 1
Fig. 1
The schedule of enrolment, interventions, and assessments. *indicates only for the key symbol used for the intervention
Fig. 2
Fig. 2
Power as a function of sample size for models with and without covariates

References

    1. Online Mendelian Inheritance in Man. Methylmalonic Aciduria Due To Methylmalonyl-Coa Mutase Deficiency 1986 [30/04/2018]. Available from: . Accessed 2 May 2019.
    1. Online Mendelian Inheritance in Man. Propionic Acidemia 2001 [04/30/2018]. Available from: . Accessed 2 May 2019.
    1. Hamilton RL, Haas RH, Nyhan WL, Powell HC, Grafe MR. Neuropathology of propionic acidemia: a report of two patients with basal ganglia lesions. J Child Neurol. 1995;10(1):25–30. doi: 10.1177/088307389501000107.
    1. Chapman KA, Summar ML. Propionic acidemia consensus conference summary. Mol Genet Metab. 2012;105(1):3–4. doi: 10.1016/j.ymgme.2011.08.007.
    1. Coude FX, Sweetman L, Nyhan WL. Inhibition by propionyl-coenzyme a of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia. J Clin Invest. 1979;64(6):1544–1551. doi: 10.1172/JCI109614.
    1. Daniotti M, la Marca G, Fiorini P, Filippi L. New developments in the treatment of hyperammonemia: emerging use of carglumic acid. Int J Gen Med. 2011;4:21–28.
    1. Yudkoff M, Ah Mew N, Payan I, Daikhin Y, Nissim I, Nissim I, et al. Effects of a single dose of N-carbamylglutamate on the rate of ureagenesis. Mol Genet Metab. 2009;98(4):325–330. doi: 10.1016/j.ymgme.2009.07.010.
    1. US Food and Drug Administration . Drug approval package: Carbaglu (Carglumic acid) tablets: U.S Food and Drug Administrations. 2010.
    1. Baumgartner MR, Horster F, Dionisi-Vici C, Haliloglu G, Karall D, Chapman KA, et al. Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia. Orphanet J Rare Dis. 2014;9:130. doi: 10.1186/s13023-014-0130-8.
    1. Signorini DF. Sample size for Poisson regression. Biometrika. 1991;78(2):446–450. doi: 10.1093/biomet/78.2.446.
    1. Hsieh FY, Bloch DA, Larsen MD. A simple method of sample size calculation for linear and logistic regression. Stat Med. 1998;17(14):1623–1634. doi: 10.1002/(SICI)1097-0258(19980730)17:14<1623::AID-SIM871>;2-S.
    1. Hsieh FY, Lavori PW. Sample-size calculations for the Cox proportional hazards regression model with nonbinary covariates. Control Clin Trials. 2000;21(6):552–560. doi: 10.1016/S0197-2456(00)00104-5.
    1. Haybittle J. Repeated assessment of results in clinical trials of cancer treatment. Br J Radiol. 1971;44(526):793–797. doi: 10.1259/0007-1285-44-526-793.
    1. Peto R, Pike M, Armitage P, Breslow N, Cox D, Howard SV, et al. Design and analysis of randomized clinical trials requiring prolonged observation of each patient. I. Introduction and design. Br J Cancer. 1976;34(6):585–612. doi: 10.1038/bjc.1976.220.
    1. Alfadhel M, Al Othaim A, Al Saif S, Al Mutairi F, Alsayed M, Rahbeeni Z, et al. Expanded newborn screening program in Saudi Arabia: incidence of screened disorders. J Paediatr Child Health. 2017;53(6):585–591. doi: 10.1111/jpc.13469.
    1. Alfadhel M, Mutairi FA, Makhseed N, Jasmi FA, Al-Thihli K, Al-Jishi E, et al. Guidelines for acute management of hyperammonemia in the Middle East region. Ther Clin Risk Manag. 2016;12:479–487. doi: 10.2147/TCRM.S93144.
    1. Fraser JL, Venditti CP. Methylmalonic and propionic acidemias: clinical management update. Curr Opin Pediatr. 2016;28(6):682–693. doi: 10.1097/MOP.0000000000000422.
    1. Vara R, Turner C, Mundy H, Heaton ND, Rela M, Mieli-Vergani G, et al. Liver transplantation for propionic acidemia in children. Liver Transpl. 2011;17(6):661–667. doi: 10.1002/lt.22279.
    1. Chakrapani A, Sivakumar P, McKiernan PJ, Leonard JV. Metabolic stroke in methylmalonic acidemia five years after liver transplantation. J Pediatr. 2002;140(2):261–263. doi: 10.1067/mpd.2002.121698.
    1. Kaplan P, Ficicioglu C, Mazur AT, Palmieri MJ, Berry GT. Liver transplantation is not curative for methylmalonic acidopathy caused by methylmalonyl-CoA mutase deficiency. Mol Genet Metab. 2006;88(4):322–326. doi: 10.1016/j.ymgme.2006.04.003.
    1. Kasahara M, Horikawa R, Tagawa M, Uemoto S, Yokoyama S, Shibata Y, et al. Current role of liver transplantation for methylmalonic acidemia: a review of the literature. Pediatr Transplant. 2006;10(8):943–947. doi: 10.1111/j.1399-3046.2006.00585.x.
    1. Nyhan WL, Gargus JJ, Boyle K, Selby R, Koch R. Progressive neurologic disability in methylmalonic acidemia despite transplantation of the liver. Eur J Pediatr. 2002;161(7):377–379. doi: 10.1007/s00431-002-0970-4.
    1. Charbit-Henrion F, Lacaille F, McKiernan P, Girard M, de Lonlay P, Valayannopoulos V, et al. Early and late complications after liver transplantation for propionic acidemia in children: a two centers study. Am J Transplant. 2015;15(3):786–791. doi: 10.1111/ajt.13027.
    1. Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, et al. Acute management of propionic acidemia. Mol Genet Metab. 2012;105(1):16–25. doi: 10.1016/j.ymgme.2011.09.026.
    1. Picca S, Bartuli A, Dionisi-Vici C. Medical management and dialysis therapy for the infant with an inborn error of metabolism. Semin Nephrol. 2008;28(5):477–480. doi: 10.1016/j.semnephrol.2008.05.007.
    1. Filippi L, Gozzini E, Fiorini P, Malvagia S, la Marca G, Donati MA. N-carbamylglutamate in emergency management of hyperammonemia in neonatal acute onset propionic and methylmalonic aciduria. Neonatology. 2010;97(3):286–290. doi: 10.1159/000255168.
    1. de Baulny HO, Benoist JF, Rigal O, Touati G, Rabier D, Saudubray JM. Methylmalonic and propionic acidaemias: management and outcome. J Inherit Metab Dis. 2005;28(3):415–423. doi: 10.1007/s10545-005-7056-1.
    1. Gebhardt B, Dittrich S, Parbel S, Vlaho S, Matsika O, Bohles H. N-carbamylglutamate protects patients with decompensated propionic aciduria from hyperammonaemia. J Inherit Metab Dis. 2005;28(2):241–244. doi: 10.1007/s10545-005-5260-7.
    1. Jones S, Reed CA, Vijay S, Walter JH, Morris AA. N-carbamylglutamate for neonatal hyperammonaemia in propionic acidaemia. J Inherit Metab Dis. 2008;31(Suppl 2):S219–S222. doi: 10.1007/s10545-008-0777-1.
    1. Levrat V, Forest I, Fouilhoux A, Acquaviva C, Vianey-Saban C, Guffon N. Carglumic acid: an additional therapy in the treatment of organic acidurias with hyperammonemia? Orphanet J Rare Dis. 2008;3:2. doi: 10.1186/1750-1172-3-2.
    1. Ah Mew N, McCarter R, Daikhin Y, Nissim I, Yudkoff M, Tuchman M. N-carbamylglutamate augments ureagenesis and reduces ammonia and glutamine in propionic acidemia. Pediatrics. 2010;126(1):e208–e214. doi: 10.1542/peds.2010-0008.
    1. Guffon N, Gessler P, Galloway P, Martinez-Pardo M, Meli C, Mulder F. M, et al. treatment of NAGS deficiency: retrospective data on 23 patients treated with carglumic acid over 16 years. Mol Genet Metab. 2011;102(3):286–287.
    1. US Food and Drug Administration . Carbaglu® prescribing information. 2010.
    1. European Medical Agency . Committee for Medicinal Products for human use (CHMP), editor. EMA/532759/2016 ed. London: European Medications Agency; 2016. Assessment report for paediatric studies submitted according to article 46 of the regulation (EC) no 1901/2006: Carbaglu - carglumic acid; pp. 1–26.
    1. Burlina A, Cazzorla C, Zanonato E, Viggiano E, Fasan I, Polo G. Clinical experience with N-carbamylglutamate in a single-Centre cohort of patients with propionic and methylmalonic aciduria. Mol Genet Metab Rep. 2016;8:34–40. doi: 10.1016/j.ymgmr.2016.06.007.
    1. Tummolo A, Melpignano L, Carella A, Di Mauro AM, Piccinno E, Vendemiale M, et al. Long-term continuous N-carbamylglutamate treatment in frequently decompensated propionic acidemia: a case report. J Med Case Rep. 2018;12(1):103. doi: 10.1186/s13256-018-1631-1.

Source: PubMed

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