Efficacy, safety and population pharmacokinetics of sapropterin in PKU patients <4 years: results from the SPARK open-label, multicentre, randomized phase IIIb trial
- Ania C. Muntau1Email author,
- Alberto Burlina2,
- François Eyskens3,
- Peter Freisinger4,
- Corinne De Laet5,
- Vincenzo Leuzzi6,
- Frank Rutsch7,
- H. Serap Sivri8,
- Suresh Vijay9,
- Milva Orquidea Bal10,
- Gwendolyn Gramer11,
- Renata Pazdírková12,
- Maureen Cleary13,
- Amelie S. Lotz-Havla14,
- Alain Munafo15,
- Diane R. Mould16,
- Flavie Moreau-Stucker17 and
- Daniela Rogoff17
© The Author(s). 2017
Received: 5 August 2016
Accepted: 23 February 2017
Published: 9 March 2017
Sapropterin dihydrochloride, a synthetic formulation of BH4, the cofactor for phenylalanine hydroxylase (PAH, EC 22.214.171.124), was initially approved in Europe only for patients ≥4 years with BH4-responsive phenylketonuria. The aim of the SPARK (Safety Paediatric efficAcy phaRmacokinetic with Kuvan®) trial was to assess the efficacy (improvement in daily phenylalanine tolerance, neuromotor development and growth parameters), safety and pharmacokinetics of sapropterin dihydrochloride in children <4 years.
In total, 109 male or female children <4 years with confirmed BH4-responsive phenylketonuria or mild hyperphenylalaninemia and good adherence to dietary treatment were screened. 56 patients were randomly assigned (1:1) to 10 mg/kg/day oral sapropterin plus a phenylalanine-restricted diet or to only a phenylalanine-restricted diet for 26 weeks (27 to the sapropterin and diet group and 29 to the diet-only group; intention-to-treat population). Of these, 52 patients with ≥1 pharmacokinetic sample were included in the pharmacokinetic analysis, and 54 patients were included in the safety analysis. At week 26 in the sapropterin plus diet group, mean phenylalanine tolerance was 30.5 (95% confidence interval 18.7–42.3) mg/kg/day higher than in the diet-only group (p < 0.001). The safety profile of sapropterin, measured monthly, was acceptable and consistent with that seen in studies of older children. Using non-linear mixed effect modelling, a one-compartment model with flip-flop pharmacokinetic behaviour, in which the effect of weight was substantial, best described the pharmacokinetic profile. Patients in both groups had normal neuromotor development and stable growth parameters.
The addition of sapropterin to a phenylalanine-restricted diet was well tolerated and led to a significant improvement in phenylalanine tolerance in children <4 years with BH4-responsive phenylketonuria or mild hyperphenylalaninemia. The pharmacokinetic model favours once per day dosing with adjustment for weight. Based on the SPARK trial results, sapropterin has received EU approval to treat patients <4 years with BH4-responsive phenylketonuria.
ClinicalTrials.gov, NCT01376908. Registered June 17, 2011.
KeywordsSapropterin Phenylalanine hydroxylase Phenylketonuria Hyperphenylalaninemia Pharmacokinetics SPARK
Hyperphenylalaninemia (HPA) is a rare inherited metabolic disorder caused by reduced activity of the hepatic enzyme phenylalanine hydroxylase (PAH, EC 126.96.36.199), which catalyses the conversion of phenylalanine (Phe) to tyrosine. Most cases of HPA (98%) in North American and European populations are due to mutations in the PAH gene but, in rare cases of HPA (1–2%), the cause can be a defect in the metabolism of the natural PAH cofactor, the R diastereoisomer of tetrahydrobiopterin (BH4) [1–3]. Owing to the reduced activity of PAH due to either mechanism, patients with HPA have an accumulation of Phe in the blood and body tissues and a relative deficiency of tyrosine and subsequent metabolites such as epinephrine [4, 5].
HPA can present with a spectrum of phenotypes that can be grouped into three main categories according to blood Phe concentrations before therapeutic intervention: classical PKU (Phe >1200 μmol/L); mild PKU (Phe 600–1200 μmol/L); mild HPA (Phe 120–600 μmol/L) [2, 5, 6]. PKU can lead to cognitive impairment and, if untreated, patients can develop mild-to-severe intellectual disability and other neurological sequelae [2, 5, 7].
The therapeutic range of Phe concentration varies according to different guidelines [8, 9], and there is no international consensus. The US diagnostic and management guidelines recommend that the initiation of treatment for PKU should be undertaken as early as possible, preferably within the first week after birth, with a goal of having blood Phe in the range 120–360 μmol/L within the first 2 weeks of life, to prevent permanent neurological damage . The European guidelines recommend target concentrations of 120-360 μmol/L for individuals aged 0-12 years and for maternal PKU . In both, this is largely achieved by a natural protein-restricted diet and Phe-free synthetic amino-acid supplementation [10, 11]. However, adherence to a Phe-restricted diet is burdensome owing to the need for long-term dietary counselling and daily micronutrient supplementation . The management guidelines also stipulate that a course of treatment with BH4 should be investigated [10, 11].
Sapropterin dihydrochloride (sapropterin, Kuvan®, Merck, Geneva, Switzerland, an affiliate of Merck KGaA, Darmstadt, Germany, and BioMarin, Novato, CA, USA) is a synthetic formulation of BH4 that has been shown to be effective in lowering serum Phe concentrations and/or improving dietary Phe tolerance in a subset of patients with PKU or mild HPA who respond to treatment with BH4 (known as responders) and in the rare patients with a defect in BH4 synthesis . Based on the results of the SPARK (Safety Paediatric efficAcy phaRmacokinetics with Kuvan®) study, the European Medicines Agency has recently extended the indication for sapropterin from the treatment of BH4-responsive PKU in adults and children aged ≥4 years and in all BH4-deficient adults and children [12, 13] to now include children with BH4-responsive PKU <4 years old, for whom the previous standard of care was a Phe-restricted diet.
The primary aim of the SPARK study was to evaluate the efficacy (increase in Phe tolerance, defined as the amount of Phe a patient may consume while maintaining blood Phe concentrations within the target range of 120–360 μmol/L); safety of 26 weeks of treatment with sapropterin dihydrochloride plus a Phe-restricted diet compared with a Phe-restricted diet alone in children <4 years of age with BH4-responsive PKU or mild HPA; to document the relationship between exposure and response; and to support the posology in this age-group. Although population pharmacokinetic (PopPK) data for sapropterin have been published for infants and young children in the USA and Canada , there are no PopPK data for sapropterin in this age range in the European Union (EU); therefore, a secondary aim of SPARK was to develop a PopPK model for sapropterin in this population. The other secondary endpoints were to document the concentrations of blood Phe during the study and extension periods, to document the change in dietary Phe tolerance, and to monitor blood pressure, growth parameters, and neuromotor developmental milestones.
The SPARK trial (NCT01376908) is a 26-week open-label, multicentre, randomized phase IIIb study to assess the efficacy, safety and PopPK of sapropterin in patients aged <4 years with BH4-responsive PKU or mild HPA. SPARK was conducted at 22 sites in nine countries: Austria (n = 2), Belgium (n = 2), Czech Republic (n = 1), Germany (n = 4), Italy (n = 5), Netherlands (n = 2), Slovakia (n = 3), Turkey (n = 1) and the United Kingdom (n = 2). The study was performed in accordance with the protocol and subsequent protocol amendments and with the ethical principles laid down in the Declaration of Helsinki, in accordance with the International Conference on Harmonisation (ICH), Note for Guidance on Good Clinical Practice (ICH Topic E6, 1996) and applicable regulatory requirements. The local ethics committee/institutional review board at each of the participating centres approved the protocol.
Male or female patients aged <4 years at randomization were eligible for entry into the study if they had participated in the screening protocol <42 days before study day 1, had a confirmed diagnosis of mild HPA or PKU (a defined level of Phe tolerance consistent with a diagnosis of PKU, ≥2 previous blood Phe concentrations ≥400 μmol/L obtained on two separate occasions), were responsive to BH4 (a decrease of >30% in Phe concentrations following a 20 mg/kg BH4 challenge of at least 24 h), good adherence to dietary treatment and maintenance of blood Phe concentrations within the therapeutic target range (120–360 μmol/L) for 4 months prior to screening or at least the last four values of Phe (either from venous blood or dry blood spot) were to be assessed, out of which 75% had to be within the above therapeutic range. Patients were excluded if they had used sapropterin or any preparation of BH4 within the previous 30 days (unless for the purposes of the BH4 responsiveness test), had known hypersensitivity to sapropterin, its excipients, or to other approved or non-approved formulations of BH4, or had a previous diagnosis of BH4 deficiency.
Patients’ parent(s)/guardian(s) gave written informed consent for participation in the study before any trial-related procedures were performed. Parent(s) and/or guardian(s) had to be willing to comply with all study procedures, maintain strict adherence to the diet, and be willing and able to provide written, signed informed consent after the nature of the study had been explained and prior to any study procedures. Where required, separate informed consent was obtained from the patients’ parents or guardians to obtain samples for pharmacokinetic analysis.
Algorithm for phenylalanine (Phe) intake adjustments according to mean Phe concentrations
Mean Phe concentration, μmol/L
Phe intake adjustment
At Week 2
Increase by 5 mg/kg/day
No adjustment required
No adjustment required, but monitor concentration at next visit
Increase by 15 mg/kg/day
Increase by 10 mg/kg/day
Increase by 5 mg/kg/day
No change in dietary Phe intake
Determine if the subject had one or more previous dietary Phe intake increases
• If so, remove the dietary Phe in the order that it was previously increased, beginning with the amount of the last increase
• If not, no adjustment required
If this is first occasion at this concentration, monitor concentration at the next visit and if second occasion is at this concentration, provide dietary counseling
If this is first occasion at this concentration, provide dietary counseling and monitor concentration at the next visit and if second occasion is at this concentration, provide dietary counseling and terminate from the trial
Blood Phe concentrations were measured twice weekly via dried blood spot cards using a high-performance liquid chromatography/tandem mass spectrometry method for Phe detection. The results were verified every 3 months using venous blood plasma. Blood Phe samples could be obtained more frequently at the investigator’s discretion.
Secondary endpoints included neuromotor development and physical growth parameters (height or length, weight and maximal occipital-frontal head circumference). Neuropsychological development was assessed using the adaptive behaviour composite score with the Bayley III and the social-emotional composite score in the WPPSI-III, although these results are not reported in this manuscript.
The PopPK analysis population comprised all randomized subjects with ≥1 pharmacokinetic sample. PopPK parameters were apparent clearance (CL/F), apparent volume of distribution (V/F), absorption rate constant (Ka), and endogenous BH4 (C0). These were used to compute the area under the curve (AUC0–∞), peak serum concentration (Cmax), time of Cmax (Tmax), and half-life (t1/2). Plasma samples were collected for endogenous BH4 measurement at baseline and sparsely thereafter between weeks 5–12 after oral administration of sapropterin 10 mg/kg/day. In order to ensure that the sparse pharmacokinetic sampling provided sufficient information and that samples were taken at informative times, the sampling had been planned using D-optimization . During this process, competing maturation functions were considered [16, 17].
PopPK modelling was conducted using NONMEM® (software version 7, level 2; Icon Development Solutions, Ellicott City, MD, USA) using standard model building and evaluation approaches. Covariates, including age, weight and sex, were evaluated using standard methodology to determine if these factors were predictive of BH4 pharmacokinetics. The final model was subsequently used to derive metrics of exposure and to determine the exposure relative to adult PKU patients.
All standard blood chemistry, hematologic and urine analysis, as well as specialized testing for Phe and tyrosine concentrations, were performed at a central laboratory.
The safety population consisted of all subjects who had some safety assessment data available. Safety was assessed at the clinic on a monthly basis during the 26-week study period or until 4 weeks post-treatment, by recording, reporting, and analysis of baseline medical conditions and adverse events (AEs) and physical examination findings (including vital signs). Standard blood chemistry, hematologic, and urine analyses were performed every 3 months during the study period for safety analysis.
PAH genotype data were collected at screening for enrolled patients, after a separate informed consent was obtained from the patients’ parents or guardians. Genotype testing was performed by a central laboratory.
The primary efficacy analysis population was the intention-to-treat (ITT) population comprising all randomized patients. The per-protocol (PP) population included all ITT patients who completed the study with no prohibited concomitant medication and without major protocol deviation. A missing pre-study Phe tolerance, lack of adherence to Phe-restricted diet over the past 3 months, lack of adherence to sapropterin, and a sapropterin-dose adjustment not conducted as per protocol were considered to be major protocol deviations leading to exclusion from the PP population. The safety population comprised all patients with safety assessment data available (≥1 visit for vital signs, AEs or laboratory results) and who had received ≥1 dose of sapropterin or were randomly assigned to Phe-restricted diet alone.
The sample size was planned to be 23 patients per group, to ensure a power of 80% to demonstrate a treatment group difference, assuming a dietary Phe tolerance of 20 mg/kg/day under dietary therapy alone, a difference of 75% with the sapropterin plus diet group, and a common standard deviation of 17.5 mg/kg/day. To compensate for possible dropouts, a total of 50 subjects were to be randomized.
The dietary Phe tolerance was analyzed using the repeated measures analysis of covariance (ANCOVA) on the observed records for the ITT population, with baseline Phe tolerance, treatment group, age group, visit, baseline blood Phe concentration and treatment by visit interaction as fixed effects. Secondary endpoints were described using summary statistics.
Non-linear mixed-effect modelling (NONMEM® software version 7, level 2) was applied to estimate the pharmacokinetic parameters and their variability. The final model was evaluated using a number of methods, which included bootstrapping and visual predictive checks, as conducted previously in children aged 0–6 years .
In order to evaluate the differences in exposure expected from the original model and the current model, simulated concentration–time profiles for the reference subject were generated.
Patient disposition and demographics
Demographic and baseline characteristics (ITT population)
Sapropterin + Phe- restricted diet (n = 27)
Phe-restricted diet only (n = 29)
Age group, n (%)
12 − <24 months
24 − <48 months
Males, n (%)
Age at PKU diagnosis, days
Blood Phe concentration at diagnosis, μmol/L
879.9 ± 596.5
PKU severitya n (%)
The overall mean adherence to sapropterin (defined as the proportion between the actual dose administered and the prescribed dose) over the study was 100% (range 82 to 107%). Most patients (n = 25, 92.6%) continued on 10 mg/kg/day after 4 weeks of treatment, with only two patients switching to 20 mg/kg/day. The overall mean (±SD) adherence to diet, as assessed by a 3-day food diary, was 94.6±9.4% (range 69 to 111%) in the sapropterin-treated group and 92.1±23.8% (range 65 to 183%) in the diet-only treated group.
Dietary Phe tolerance after 26 weeks
Blood Phe concentrations
Phe concentrations from dried blood spots were lower than those from venous blood spots but this was consistent with differences reported in the literature [19–21]. In the Phe-restricted diet group, the adjusted mean blood Phe concentrations in the ITT population were stable over time, with a mean (±SD) increase of 23.1 (±21.9) μmol/L at week 26 (Fig. 2b). In the sapropterin plus Phe-restricted diet group, the mean (±SD) blood concentrations decreased by 110.7 (±20.1) μmol/L at week 4 and gradually returned to concentrations similar to those seen in the Phe-restricted diet group, reflecting the increase in Phe intake and Phe tolerance. At week 26, the adjusted mean (±SD) blood Phe concentrations were similar: 300.1 (±115.2) μmol/L in the sapropterin plus Phe-restricted diet group and 343.3 (±118.4) μmol/L in the diet-only group (adjusted between-group difference 33.2 μmol/L [95% CI −94.8, 28.4], p = 0.290). It is important to note that patients were expected to maintain blood Phe concentrations within this range; therefore, differences in blood Phe concentrations were not anticipated.
The observed proportion of patients with blood Phe concentrations maintained in the range 120–360 μmol/L throughout the whole study was greater in the sapropterin plus Phe-restricted diet group (n = 9/27, 33.3%) than in the diet-only group (n = 3/29, 10.3%). 21 of 27 (77.8%) sapropterin-treated patients and 15 of 27 (55.6%) patients on only the Phe-restricted diet had ≥1 blood Phe concentration at or below the 120 μmol/L threshold established by the British PKU Registry . However, very few instances of Phe concentration below the normal range thresholds of 40 and 26 μmol/L were observed during the study.
Change from baseline in dietary Phe tolerance
The mean change in dietary Phe tolerance between baseline and the last Phe tolerance observation was assessed within each treatment group. The mean (±SD) change from baseline to week 26 in patients receiving sapropterin plus Phe-restricted diet was 36.9 (±27.3) mg/kg/day (p < 0.001). The mean change from baseline in patients only on the Phe-restricted diet was 13.1 (±19.6) mg/kg/day (p = 0.002).
Parameter estimates for final model
Coefficient describing effect of weight on CL/F
Coefficient describing effect of weight on V/F
Residual error (%CV)
From the model, an elimination half-life of approximately 1 h can be computed, with an absorption half-life (ln2/Ka) of approximately 3 h, suggesting flip-flop kinetics where the absorption becomes the rate-limiting step of drug disposition.
Effect of weight on clearance and volume of distribution
% of reference
% of reference
Overall, the exposure across all age groups is comparable, although the number of patients in all age groups is small. The exposure in pediatric patients was lower than the expected exposure in adults, based on the simulated concentration–time profiles following the 10 mg/kg/day dose across a range of body weights. This analysis shows that the concentrations remain above the endogenous concentration, which is set at a concentration below that for a person not diagnosed with PKU, for a daily dose interval and support the current approach to treatment as conservative (Fig. 4).
Summary of safety data showing the proportion of patients reporting adverse events (AEs) (Safety population)
Sapropterin + Phe-restricted diet (n = 27)
Phe-restricted diet alone (n = 27)
Patients, n (%)
Patients, n (%)
AEs related to sapropterin
Infections and infestations related to sapropterin
Gastrointestinal disorders related to sapropterin
Amino acid concentrations decrease related to sapropterin
AEs leading to discontinuation
The most common TEAEs in the sapropterin plus Phe-restricted diet group and in the Phe-restricted diet group were: pyrexia (63.0 and 66.7%), cough (48.1 and 48.1%) and nasopharyngitis (48.1 and 40.7%), respectively. The most common TEAEs classified as related to sapropterin were amino acid concentration decrease (six patients [22.2%]), rhinitis, and vomiting (two patients each [7.4%]), and one patient (3.7%) each for pharyngitis, diarrhea, abdominal pain, mouth ulceration and increased amino acid concentration.
Although the proportion of patients who reported a serious AE (SAE) was higher in the sapropterin plus Phe-restricted diet group compared with the Phe-restricted diet (11.1 vs. 3.7%), all SAEs were assessed as unrelated to sapropterin treatment (Table 5).
Of 109 patients who were screened, 73 agreed to participate in the pharmacogenetics sub-study. Of the 73 patients who agreed, 36 were screening failures, leaving genotype data for 37 responders (Additional file 1: Table S1).
Neuromotor development and growth parameters
Most patients in both treatment groups had normal neuromotor development, including fine motor, gross motor, language, and personal and social function, and there were no statistically significant differences between treatment groups in any of the neuromotor developmental milestones at baseline, 12 and 26 weeks (Additional file 1: Figure S1).
Patients in both treatment groups had stable growth parameters, including body mass index SD score (SDS), height SDS, maximum occipital-frontal head circumference SDS and weight SDS. There were no statistically significant differences between the treatment groups for any of the growth parameters.
In PKU, blood Phe concentrations need to be controlled from birth to prevent neurological sequelae, such as cognitive impairment and mild-to-severe intellectual disability, linked to PKU [5, 7]. Until July 2015 there was no licensed pharmacological treatment available in the EU for children with PKU aged <4 years, and the standard of care was a Phe-restricted diet. The results of the SPARK study, which was the first clinical trial of sapropterin in patients 0–4-years-old with BH4-responsive PKU or mild HPA in Europe, showed that daily dosing with 10 or 20 mg/kg/day sapropterin in combination with a Phe-restricted diet led to statistically and clinically significant improved dietary Phe tolerance at week 26 compared with a Phe-restricted diet alone, while maintaining mean blood Phe concentrations within the protocol-specified range. These results were consistent with those seen in children aged 4–12 years treated with 20 mg/kg/day sapropterin, in whom the mean amount of Phe supplement tolerated had increased at 10 weeks of treatment . The results were also consistent with those reported in a study from the USA and Canada in children aged 0–6 years old, in whom 20 mg/kg/day sapropterin treatment lowered blood Phe concentrations, enabling, in some cases, an increase in dietary Phe intake .
The benefits of initiating sapropterin therapy in patients younger than 4 years have been highlighted by a post-marketing study conducted in Japan between 1995 and 2001, which reported that all patients who started treatment with sapropterin before the age of 4 years maintained serum Phe concentrations within the recommended range for the duration of the study . Previous reports have shown that neurocognitive function was preserved and no neurodevelopmental penalty was reported in patients who started sapropterin therapy between 0 and 6 years of age , and that treatment with BH4 may enable relaxation of the dietary regimen, leading to improved quality of life . Patients with mild HPA, who comprised almost a half of the population in this study, retain substantial enzyme activity and will, therefore, likely respond to sapropterin treatment. However, the indication for treatment of mild HPA differs between countries due to weak evidence. US guidelines recommend treatment at a Phe concentration above 360 μmol/L , while other countries start treatment at Phe concentrations above 600 μmol/L .
In this study, the addition of sapropterin to a Phe-restricted diet in patients <4 years old with BH4-responsive PAH deficiency significantly improved Phe tolerance compared with a Phe-restricted diet alone. In the sapropterin-treated group, blood Phe concentrations initially fell at the beginning of treatment (4 weeks), but they slowly increased over the course of the study to reach concentrations similar to those at baseline by week 12 (Fig. 2), while increasing dietary Phe-intake. The observed increase in Phe tolerance reported in patients on the Phe-restricted diet compared with the tolerance at baseline may be explained by the fact that the patients in this group were not at their maximum Phe tolerance in daily practice before starting the study. This observation confirms the expectation that under the tight control of study conditions using a strict algorithm of Phe escalation, dietary Phe tolerance may be further optimized . Because of the potential for Phe concentrations to drop below either the normal or the desired therapeutic concentrations owing to the action of sapropterin, careful monitoring and adjustment of therapeutic dose and dietary Phe concentrations was necessary.
The pharmacokinetics of BH4 can be well described by a one-compartment model that respects the principle of parsimony and provides accurate estimates that describe BH4 profiles virtually identical to those from a two-compartment model evaluated in a previous study . The terminal and absorption half-lives are suggestive of flip-flop pharmacokinetic behavior, in which absorption is the rate-limiting step of drug disposition. Sapropterin exposure was similar across all age groups studied here. With this in mind, a once-daily dosing regimen is justified. Weight was the only covariate that had an effect on the clearance and volume distribution of sapropterin, meaning that dose adjustments based on weight are appropriate .
The secondary endpoints of growth and neuromotor development were considered to be normal in the patient population throughout the study and no difference between groups was observed, suggesting no treatment effect on these growth and development parameters. However, the time scale in the study was too short to expect clinically meaningful changes in neuromotor development.
The safety profile for sapropterin was acceptable and similar to that reported in studies of patients >4 years old  and in those <4 years old , with no deaths, severe TEAEs or withdrawals reported. Although four patients had SAEs, none of these was deemed to be related to treatment. The number of TEAEs was similar between the two groups and was commonly associated with normal childhood illness.
In conclusion, the addition of sapropterin to a Phe-restricted diet in patients aged <4 years old with BH4-responsive PKU, mild PKU or mild HPA was well tolerated and led to a significant improvement in Phe tolerance compared with only a Phe-restricted diet. The pharmacokinetics of sapropterin in patients aged <4 years are adequately described by a one-compartment model, and favor once-a-day dosing with dose adjustment for weight. These data led to the approval of sapropterin for individuals with BH4-responsive PKU or mild HPA aged <4 years, and will thus change treatment management for this subset of patients in the first week of life.
Analysis of covariance
Area under the curve
- Cmax :
Peak serum concentration
International Conference on Harmonisation
- Ka :
Adsorption rate constant
Safety paediatric efficacy pharmacokinetics with Kuvan®
- T1/2 :
- Tmax :
Time of Cmax
Apparent volume of distribution
The authors would like to thank patients, investigators, co-investigators, and the study teams at each of the participating centres and at Merck KGaA, Darmstadt, Germany and EMD Serono, Boston, MA, USA. The authors would also like to thank Anita MacDonald who contributed significantly to the design and running of the study, including suggesting changes to the protocol, dietetic monitoring requirements, and helping to recruit patients. The authors would like to acknowledge the SPARK investigators for their contribution, without whom this study would not be possible: Dr Med Michaela Brunner-Krainz (University Hospital, Graz, Austria); Professor Daniela Karall (Clinic for Pediatrics I, Innsbruck, Austria); Professor Philippe Goyens (Hôpital Universitaire des Enfants, Brussels, Belgium); Dr Patrick Verloo (UZ Gent, Belgium); Dr Giovanna Cotugno (Ospedale Pediatrico Bambino Gesù, Rome, Italy); Dr Enrica Riva (Clinica Pediatrica - Ospedale San Paolo, Milan, Italy); Dr Annet Bosch (Academisch Medisch Centrum, Amsterdam, The Netherlands); Dr Estela Rubio-Gozalbo (Maastricht Universitair Medisch Centrum; Maastricht, The Netherlands); Dr Katarina Hálová (Detská fakultná nemocnica s poliklinikou Banska Bystrica, Slovakia); Dr Ludmila Potocnakova (Detská fakultná nemocnica Kosice, Metabolická ambulancia, Kosice, Slovakia); Dr Oto Urge (Univerzitna nemocnica Bratislava, Nemocnica sv. Cyrila a Metoda, Bratislava, Slovakia); Dr Ilaria Bettocchi, Graziana D’Addabbo, Carla Musiani (Department of Pediatrics, University of Bologna, Bologna, Italy).
Finally, the authors thank Steven Goodrick and Andrew Thomson of inScience Communications, Springer Healthcare, UK (supported by Merck KGaA, Darmstadt, Germany), for assistance with the preparation of this manuscript.
This study was supported by Merck, Switzerland, an affiliate of Merck KGaA, Darmstadt, Germany.
Availability of data and materials
Data are available on request.
ACM contributed to the study design, acted as an international coordinator of the study and participated in data analysis and interpretation and in writing of the manuscript. AB performed the patient examinations. FE participated in the study as a principal investigator at his study site and was responsible for patient enrolment and coordination. PF contributed to the acquisition, analysis and interpretation of the data and was responsible for the conduct of the study at his study site. CDL contributed to the interpretation of the data. VL was involved in the acquisition, analyses and interpretation of the biochemical data. FR made a substantial contribution to the acquisition, analysis and interpretation of the data. HSS made a substantial contribution to the clinical study. SV contributed to the acquisition of the clinical data, as one of the principal investigators on the study. MOB contributed to all the clinical steps of the study. GG participated as investigator in the clinical trial and provided patient data. RP was responsible for the collection and interpretation of the data from the patients in the Czech Republic. MC was involved in the execution of the study and in the review of the study report. AL-H participated in the collection of patient data. AM contributed to the development of the population pharmacokinetic analysis plan and the interpretation of these data. DRM conducted the population PK analysis. FM-S participated in the design of the study and performed the statistical analysis. DR contributed to the review of the data. All authors were involved in the writing, revision and final approval of the manuscript of the manuscript.
ACM has participated in strategic advisory boards and has received honoraria as a consultant and as a speaker from Merck KGaA, Darmstadt, Germany. GG has received support for travel expenses to the SSIEM congress from Merck. FR has participated in advisory boards and has received honoraria as a consultant from Merck KGaA, Darmstadt, Germany. Both DR and FM-S are employees of EMD Serono, Inc, Billerica, MA, USA, a business of Merck KGaA, Darmstadt, Germany. AM is an employee of the Merck Institute for Pharmacometrics, Lausanne, Switzerland, a subsidiary of Merck KGaA, Darmstadt, Germany. AB is an advisory board member for Danone and Merck. PF has received grants from Merck. CDL has received travel fees and provided data management support. MC has been an advisory board member for, and her institution has received a grant from, Merck. A L-H has received travel grants from Merck. DRM was also a paid consultant of Merck KGaA, Darmstadt, Germany. All authors have received fees as an investigator for Merck KGaA, Darmstadt, Germany.
Consent for publication
Consent to publish has been obtained from all parents and guardians.
Ethics approval and consent to participate
The local ethics committee/institutional review board at each of the participating centres approved the protocol. Patients’ parent(s)/guardian(s) gave written informed consent for participation in the study before any trial-related procedures were performed. Ethics committee: Lead Ethics Committee of the LMU, Munich, Germany (ethikkommission.med.uni-muenchen.de).
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