Changing to burosumab, a monoclonal antibody targeting fibroblast growth factor 23, significantly improved phosphorus homeostasis, rickets, lower-extremity deformities, mobility, and growth versus continuing oral phosphate and active vitamin D (conventional therapy) in a randomized, open-label, phase 3 trial involving children aged 1–12 years with X-linked hypophosphatemia. Patients were randomized (1:1) to subcutaneous burosumab or to continue conventional therapy. We present patient-reported outcomes (PROs) from this trial for children aged ≥ 5 years at screening (n = 35), using a Patient-Reported Outcomes Measurement Information System (PROMIS) questionnaire and SF-10 Health Survey for Children. PROMIS pain interference, physical function mobility, and fatigue scores improved from baseline with burosumab at weeks 40 and 64, but changed little with continued conventional therapy. Pain interference scores differed significantly between groups at week 40 (− 5.02, 95% CI − 9.29 to − 0.75; p = 0.0212) but not at week 64. Between-group differences were not significant at either week for physical function mobility or fatigue. Reductions in PROMIS pain interference and fatigue scores from baseline were clinically meaningful with burosumab at weeks 40 and 64 but not with conventional therapy. SF-10 physical health scores (PHS-10) improved significantly with burosumab at week 40 (least-squares mean [standard error] + 5.98 [1.79]; p = 0.0008) and week 64 (+ 5.93 [1.88]; p = 0.0016) but not with conventional therapy (between-treatment differences were nonsignificant). In conclusion, changing to burosumab improved PRO measures, with statistically significant differences in PROMIS pain interference at week 40 versus continuing with conventional therapy and in PHS-10 at weeks 40 and 64 versus baseline.
Trial registration: ClinicalTrials.gov NCT02915705
X-linked hypophosphatemia (XLH) is a rare, heritable, lifelong phosphate-wasting disease. Loss-of-function mutations in the PHEX (phosphate-regulating endopeptidase homologue, X-linked) gene result in characteristic elevation of circulating fibroblast growth factor 23 (FGF23) levels, leading to reduced renal phosphate reabsorption and decreased production of active vitamin D (1,25[OH]2D) manifesting as chronic hypophosphatemia and impaired mineralization of bones and teeth, as well as muscle weakness [1, 2].
XLH typically manifests in early childhood as rickets, skeletal deformities, short stature, and in some children with dental abscesses [1,2,3,4]. Untreated or inadequately treated children commonly suffer impaired mobility and physical function, such as delayed walking, unusual gait, muscle weakness, bone, joint, and muscle pain, and emotional and social challenges [2,3,4]. Short stature acquired in childhood and skeletal deformities are irreversible, without surgery, after completion of growth. Elevated circulating FGF23 and hypophosphatemia persist into adulthood; adults often develop pseudofractures, fractures, enthesopathies, hyperparathyroidism, and early-onset osteoarthritis, and suffer increasing pain, stiffness, and loss of physical function .
For the past 40 years, therapy for XLH has primarily consisted of multiple daily doses of oral phosphate supplementation with active vitamin D (calcitriol or alfacalcidol; “conventional therapy”). Oral phosphate preparations can be unpalatable and can cause gastrointestinal symptoms, and the frequent dosing regimen is burdensome for patients and their caregivers [2, 3, 5]. Furthermore, regular monitoring and appropriate dose adjustments are needed to minimize the risk of complications of conventional therapy including nephrocalcinosis and hyperparathyroidism [1,2,3, 5].
Burosumab is a fully human monoclonal antibody (IgG1) that binds to FGF23 and inhibits its activity [6, 7]. The efficacy of burosumab in pediatric XLH has been demonstrated by increasing the levels of serum phosphorus in two phase 2 studies (UX023-CL201, NCT02163577; UX023-CL205, NCT02750618), as well as in children with rickets (rickets severity score [RSS] ≥ 2.0) in the randomized phase 3 trial of burosumab versus continued conventional therapy (UX023-CL301, NCT02915705). These trials demonstrated improvement in clinical outcomes, including rickets, lower-limb deformities, and mobility, as assessed by the 6-min walk test, with the CL301 trial demonstrating superiority of changing to burosumab over continuation of conventional therapy [2, 8, 9].
In addition to clinical outcomes, patient-reported outcome (PRO) data were collected in the phase 3 pediatric trial using Patient-Reported Outcomes Measurement Information System (PROMIS) instruments, the Short Form-10 (SF-10) Health Survey for Children, and the Faces Pain Scale—Revised (FPS-R) to quantify the impairment and compare their evolution on burosumab versus continued conventional therapy. Pain is prevalent in pediatric patients with XLH and is most frequently observed in the lower limbs, but also occurs in the back and hips . Children with XLH often have trouble performing age-appropriate gross motor activities, such as walking, running, and jumping, due to bowing of the femur, tibia, and fibula, and tibial rotation that causes the feet to turn in towards each other. Gait disturbance is common in pediatric patients with XLH, reported in > 80% of children .
Here, we present the PRO results from the phase 3 pediatric trial, specifically the endpoints of PROMIS pain interference, physical function mobility, and fatigue; health-related quality of life (HRQoL) according to SF-10; and pain intensity according to FPS-R. We also conducted a subgroup analysis to investigate whether PRO scores varied with rickets severity, sex, geographic region, or PHEX disease-causing variant.
Subjects and Methods
This open-label, randomized, active-controlled, phase 3 trial was conducted at 16 international sites with experience treating XLH. The institutional review board at each participating center approved the protocol. The trial was conducted in accordance with the Declaration of Helsinki and the Good Clinical Practice guidelines developed at the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use. Trial design details have been published previously  and are only briefly described here.
Eligibility criteria for this trial were as follows: age 1–12 years when informed consent was obtained; confirmed diagnosis of XLH according to fasting serum phosphorus < 0.97 mmol/L (3.0 mg/dL); a confirmed PHEX disease-causing variant or a variant of unknown significance in the patient, or in a directly related family member with appropriate X-linked dominant inheritance; radiographic evidence of rickets in the wrist and/or knee; a total Thacher RSS ≥ 2.0; and prior treatment with conventional therapy for ≥ 6 consecutive months (children aged < 3 years) or ≥ 12 consecutive months (children aged ≥ 3 years) up until enrollment. Parents or guardians provided written informed consent for their children to participate, and children gave written assent according to local guidelines. Patients were randomly assigned (1:1) to receive subcutaneous burosumab (starting dose 0.8 mg/kg every 2 weeks) or continue conventional therapy with oral phosphate and active vitamin D, the doses of which were titrated and individualized based on published recommendations [1, 6]. Patients received study medication for up to 64 weeks. PRO instruments were completed at baseline and at weeks 24, 40, and 64.
Patient-Reported Outcome Assessments
PROs were assessed using linguistically validated, approved instruments during the trial for patients aged ≥ 5 years only at the screening visit. PROMIS is a set of measures developed by the US National Institutes of Health to evaluate physical, mental, and social health [10, 11]. A fixed-length short-form PROMIS instrument comprising the pain interference, physical function mobility, and fatigue domains was created by selecting items from the three pediatric item banks of PROMIS (version 2.0; Online Resource, Table 2). Pain interference consisted of four items scored using five response options indicating the frequency of pain interference (“never,” “almost never,” “sometimes,” “often,” and “almost always”); physical function mobility consisted of 10 items scored using five response options to indicate severity (“with no trouble,” “with a little trouble,” “with some trouble,” “with a lot of trouble,” and “not able to do”); and fatigue consisted of eight items scored using five response options indicating the severity (“never,” “almost never,” “sometimes,” “often,” and “almost always”).
Items were selected using information from qualitative interviews of five children with XLH aged 8–12 years and their parents: one parent of an 8-year-old child with XLH and four parents of children with XLH aged 5–7 years. Item appropriateness was based on evidence from the concept elicitation, conceptual mapping, and cognitive debriefing exercises conducted as part of the qualitative interviews. The pain interference, physical function mobility, and fatigue items were well understood and found to be relevant and appropriate assessments of those concepts for the children and their parents. These qualitative data therefore established content validity of the selected PROMIS domains. An analysis of the psychometric properties of the PROMIS instrument (both the self-reported form for children aged ≥ 8 years and the parent proxy report form for children aged 5 to < 8 years) consisting of the three domains in the current trial (n = 35; children aged 5–12 years) confirmed it to be a reliable, valid, and responsive method for use in clinical trials in children with XLH .
The PROMIS domains were each measured at study assessment visits using a recall period of the previous 7 days. Children aged ≥ 8 years at screening completed a self-reported PROMIS instrument. For children aged 5 to < 8 years at screening, the parent or legal guardian completed the parent proxy version of the PROMIS instrument throughout the trial. PROMIS data were uploaded to the PROMIS online scoring system  to obtain the final scores for each domain. All raw scores generated from the PROMIS instrument were translated into standardized scores (termed T-scores), based on a calibration sample resulting in a calibration population mean of 50 and standard deviation (SD) of 10. The calibration sample consisted of a US cohort of 4,129 children aged 8–17 years, with 55% aged 8–12 years. The majority of children in the calibration sample (94%) were recruited from hospital-based general pediatric and subspecialty clinics, with 6% from school settings; 35% had consulted a clinician for a chronic illness diagnosis or treatment within 6 months, and 9% had two or more chronic illnesses (the most common chronic conditions were asthma, affecting 18% of children, followed by attention-deficit disorder/attention-deficit hyperactivity disorder [ADHD], arthritis, and gastrointestinal disorders) . Higher scores on the PROMIS pain interference and fatigue domains indicate greater detriment (i.e., worse pain and more fatigue), whereas a higher score on the PROMIS physical function mobility domain indicates less detriment (i.e., better physical function mobility).
Overall HRQoL was assessed using the SF-10 Health Survey for Children, a validated 10-item, caregiver-completed questionnaire designed to assess physical and psychosocial HRQoL in healthy and ill children. Each question has five response options (“Excellent,” “Very good,” “Good,” “Fair,” and “Poor”) with a recall period of the past 4 weeks. Responses were used to generate two component summary scores: physical health score (PHS-10) and psychosocial health score (PSS-10), scored according to published methods . The scale was scored so that a score of 50 corresponds to the average score in a 2006 sample, which comprised a combination of children from the general population and a supplemental sample with disability and chronic conditions; higher global scores are associated with better HRQoL.
The FPS-R was used to assess current pain at each study visit. The self-reported scale uses graphical facial representations of pain to allow self-reporting of current pain intensity at rest (not during or immediately after physical activity) on a 0–10 scale (0 = no hurt to 10 = hurts worst; even numbers only) and has been validated in children aged 5–16 years .
The primary endpoint for this trial, namely change in rickets severity from baseline to week 40, has been reported previously . Changes from baseline in PROMIS scores were assessed as secondary endpoints, and changes from baseline in SF-10 PHS-10 and PSS-10 were assessed as exploratory endpoints. Here, we report data for changes to week 64 to provide longer-term information on XLH in children. SAS® software version 9.4 or higher (SAS Institute, Cary, NC, USA) was used for statistical analyses.
PRO endpoints were analyzed using a generalized estimating equation repeated-measures analysis. Treatment, visit, and interaction of treatment-by-visit were included as categorical variables, and baseline measures and baseline total RSS stratification factor were included as independent variables in the model. Total RSS was used in this model, as it has been validated in 52 children with XLH, with higher total RSS associated with greater impairment in walking ability as assessed by the 6-min walk test . Data for model-based estimates of the changes from baseline, standard error (SE), and corresponding 95% confidence intervals (CIs) were assessed for significance at the 5% level. Missing data were treated as missing for all analyses. Only data for patients with a baseline measurement and at least one post-baseline measurement were included in analyses of change from baseline.
As the trial was not powered to assess differences in between-group changes beyond the primary endpoint, within-group changes from baseline were reported for variables with nonsignificant between-group differences. A change of 2–3 points is considered clinically meaningful for PROMIS pediatric scales . To interpret within-group trial results, clinically relevant differences were explored based on a minimally important difference (MID) threshold of 3 points .
In an exploratory analysis, testing for treatment-by-subgroup was used to detect treatment effect heterogeneity across four subgroups (RSS: ≤ 2.5, > 2.5; sex: male, female; region: Japan, rest of world; PHEX status: clearly pathogenic PHEX variants, or likely pathogenic/variant of unknown significance) on the PRO domains using week 40 and week 64 data.
PRO assessments were completed (by the child or their parent/guardian) for all participants aged ≥ 5 years at screening, which included 15/29 patients in the burosumab group and 20/32 patients in the conventional therapy group. Baseline assessments occurred at randomization for all participants after a 7-day washout period from prior conventional therapy. Baseline characteristics for all participants (patients aged 1–12 years at screening) and those aged ≥ 5 years at screening are presented in Table 1. Overall, baseline characteristics were similar between the two age cohorts; however, serum 1,25(OH)2D concentration was lower in the cohort aged ≥ 5 years than in the total patient group (mean ± SD: 91 ± 36 vs 103 ± 43 pmol/L, respectively), particularly in the burosumab group (96 ± 38 vs 110 ± 48 pmol/L) (Table 1). Patients aged ≥ 5 years had received conventional therapy for a mean of 5.54 years.
PROMIS Pain Interference
Higher scores on the pain interference domain reflect pain having a greater impact on daily activities, with decreases in scores reflecting improvements in this domain. At baseline, the mean ± SD pain interference T-score was 53.1 ± 10.95 for burosumab and 49.9 ± 12.02 for continued conventional therapy, broadly comparable to the mean of the calibration sample of 50 . Eight of the 35 patients (23%) had pain interference scores ≥ 1 SD higher (worse) than the calibration sample average (Fig. 1a). Pain interference score decreased from baseline in the burosumab group (least-squares [LS] mean [SE] change: − 5.31 [1.705] at week 40 and − 3.55 [1.873] at week 64), indicating reduced levels of pain interference, but changed little in the group who continued to receive conventional therapy (− 0.29 [1.539] at week 40 and − 1.29 [1.267] at week 64). The change in pain interference score exceeded the 3-point MID threshold in patients receiving burosumab at both weeks 40 and 64, consistent with a clinically meaningful reduction in pain interference for this group. The change from baseline in the group continuing conventional therapy was less than the 3-point MID threshold. Burosumab was associated with a significantly greater change from baseline than conventional therapy at week 40 (between-group difference − 5.02, 95% CI − 9.29 to − 0.75; p = 0.0212) but not at week 64 (− 2.26, 95% CI − 6.61 to + 2.09; p = 0.3091) (Fig. 2a). Descriptive item-level results at baseline and week 64 can be found in the appendix (Online Resource, Table 3).
PROMIS Physical Function Mobility
Higher scores on the PROMIS physical function mobility domain indicate less detriment (i.e., better physical function mobility), with increases in scores reflecting improvements in this domain. At baseline, the mean ± SD physical function mobility T-score was 45.2 ± 9.05 for burosumab and 45.5 ± 9.86 for continued conventional therapy, similar to the mean of 50 of the calibration sample . Twelve of the 35 patients (34%) had impaired physical function indicated by physical function mobility scores ≥ 1 SD lower (worse) than the calibration sample average (Fig. 1b). Physical function mobility score increased numerically from baseline in the burosumab group (LS mean [SE]: + 2.78 [1.336] at week 40 and + 2.82 [1.648] at week 64), indicating improved physical function mobility, but showed little change in the continued conventional therapy group (+ 0.10 [0.966] at week 40 and + 0.92 [0.962] at week 64). Neither group had achieved a meaningful change from baseline based on a 3-point MID. Differences between treatment groups were not statistically significant at either week 40 (+ 2.68, 95% CI − 0.52 to + 5.89; p = 0.1009) or week 64 (+ 1.90, 95% CI − 1.80 to + 5.59; p = 0.3145) (Fig. 2b). Descriptive item-level results at baseline and week 64 can be found in the appendix (Online Resource, Table 3).
Higher scores on the PROMIS fatigue domain reflect greater levels of fatigue, with decreases in scores reflecting improvements in this domain. At baseline, the mean ± SD fatigue T-score was 48.8 ± 9.60 for burosumab and 47.0 ± 13.70 for continued conventional therapy, similar to the mean of 50 of the calibration sample . Seven of the 35 patients (20%) had fatigue scores at least 1 SD higher (worse) than the calibration sample average (Fig. 1c). Fatigue scores decreased from baseline to weeks 40 and 64 in burosumab-treated patients (LS mean [SE], − 4.29 [1.709] at week 40 and − 3.65 [2.119] at week 64), reflecting reduced levels of fatigue, but showed little change in those continuing to receive conventional therapy (LS mean [SE], − 1.05 [1.754] at week 40 and − 2.57 [1.547] at week 64). Meaningful change from baseline was achieved for the burosumab group at weeks 40 and 64, based on a 3-point MID. There was no meaningful change for the conventional therapy group at weeks 40 or 64. Between-group differences did not reach statistical significance at either week 40 (− 3.25, 95% CI − 7.86 to + 1.37; p = 0.1676) or week 64 (− 1.08, 95% CI − 6.21 to + 4.06; p = 0.6810) (Fig. 2c). Descriptive item-level results at baseline and week 64 can be found in the appendix (Online Resource, Table 3).
SF-10 Health Survey for Children
The trial population had baseline scores below the 25th percentile for PHS-10 (mean [SD] score; 40.47 [13.14] total population, 40.03 [10.07] burosumab, 40.74 [15.30] conventional therapy) and below the 50th percentile for PSS-10 (mean [SD] score; 51.92 [9.42] total population, 50.76 [9.65] burosumab, 52.79 [9.40] conventional therapy) (Fig. 3). Patients receiving burosumab showed significant improvements in LS mean (SE) PHS-10 scores from baseline at both week 40 (+ 5.98 [1.79]; p = 0.0008) and week 64 (+ 5.93 [1.88]; p = 0.0016) (Fig. 4a). By contrast, there were no statistically significant changes from baseline in the conventional therapy group at week 40 (+ 1.65 [2.17]) or week 64 (+ 0.44 [2.22]). The LS mean (SE) differences between the burosumab and continued conventional therapy groups did not meet statistical significance at either week 40 (+ 4.33 [2.82]) or week 64 (+ 5.49 [2.91]). There were no statistically significant changes in LS mean (SE) PSS-10 scores from baseline to weeks 40 or 64 for either burosumab (+ 1.53 [1.52] and + 0.94 [1.176], respectively) or continued conventional therapy (− 0.66 [1.38] and + 1.44 [1.21], respectively), with no significant differences between the two treatment groups (LS mean difference [SE]: + 2.19 [2.10] at week 40; − 0.50 [2.12] at week 64) (Fig. 4b).
Faces Pain Scale—Revised
Most children in both treatment groups reported no pain at baseline, week 40, or week 64 according to the FPS-R. Median FPS-R scores were 0 at all time points for both groups, and there were no significant differences between groups (p = 0.8786).
Treatment effect heterogeneity was assessed for the trial population in predefined subgroups: RSS: ≤ 2.5 (n = 22), > 2.5 (n = 39); sex: male (n = 27), female (n = 34). Data by region (Japan [n = 5], rest of world [n = 56]) and PHEX status (clearly pathogenic PHEX variant [n = 55], or PHEX variants that were likely pathogenic/variant of unknown significance [n = 6]) were removed from this analysis because of the imbalance in patient numbers in these groups. No statistically significant interactions (p < 0.05) were identified among the five PRO domains for the RSS and sex subgroup categories.
Children with XLH whose PRO scores indicate pain interference, fatigue, physical function mobility impairment, and reduced HRQoL despite conventional therapy would benefit from a disease-modifying treatment that alleviates the disorder’s long-term physical and psychosocial complications . Our phase 3 CL301 trial demonstrated that burosumab results in greater improvement in phosphorus homeostasis, growth, lower-extremity deformities, and healing of rickets in children with XLH compared with continuing conventional therapy . In the present analyses, we determined the impact of switching from conventional therapy to burosumab treatment compared to continuing conventional therapy on PROs of pain interference, physical function mobility, fatigue, and HRQoL.
Baseline PROMIS pain interference, physical function mobility, and fatigue scores were similar to the PROMIS calibration sample, which included 4,129 children primarily from hospital-based general pediatric and subspecialty clinics. In this sample, 35% of children had consulted a clinician for a chronic illness diagnosis or treatment within 6 months, and 9% had two or more chronic illnesses . Baseline PROMIS pain interference, physical function mobility, and fatigue scores were similar to those reported for other lifetime diseases that start in childhood, such as sickle cell disease, Crohn disease, juvenile arthritis, juvenile dermatomyositis, chronic kidney disease, or systemic lupus erythematosus [20,21,22,23,24,25,26,27].
Baseline SF-10 scores indicate impaired HRQoL in the present trial population, especially with regard to physical health, with lower baseline PHS-10 scores (mean score, 40.03) than those seen in children with asthma, attention-deficit hyperactivity disorder, depression, or learning disabilities (mean range, 43.83–48.23) . However, SF-10 is a caregiver-completed questionnaire, which may underestimate the child’s health and well-being . The FPS-R tool is validated to assess current pain, though it has not been psychometrically validated specifically in children with XLH. At all study visits, the XLH patients indicated no pain, suggesting that the FPS-R assessment of current pain at rest may not reliably assess the burden of pain severity in this population.
In patients who received burosumab, the decrease from baseline in pain interference was significantly greater than in those who continued conventional therapy, although only up to week 40. The improvement with burosumab was not fully sustained from week 40 to week 64 but did not return to baseline levels. The lack of a persistent benefit with burosumab up to week 64 may be explained by small patient numbers and possible increased activity-related pain for patients who had received early benefit from burosumab. Furthermore, pain and its associated impact in XLH is complex and multifactorial [1, 4], and expected improvements in bone health with burosumab may not be sufficient to fully address all aspects of pain syndrome over a short period of time.
Improvements from baseline in the PROMIS physical function mobility and fatigue domains were also achieved with burosumab versus conventional therapy, although the differences between groups were not statistically significant. Patients receiving burosumab did have clinically meaningful changes (based on 3-point MIDs) in two of the three PROMIS domains (pain interference and fatigue) by week 40, which were maintained at week 64. Burosumab also significantly improved the physical health domain (PHS-10) by approximately 10% at week 40, which was maintained at week 64. In patients receiving conventional therapy, changes in physical health from baseline were not seen; differences between treatment groups did not reach statistical significance, although the trial was not powered to show differences in these endpoints. There were no statistically significant interactions among the five PRO domains for the predefined subgroup categories investigated (RSS and sex).
Improvements in PROs are reflected by mobility data from the 6-min walk test reported in the primary manuscript . These data showed that patients randomized to burosumab had significantly greater improvements from baseline in percent predicted distance walked over 6 min than those continuing to receive conventional therapy at week 64 (LS mean change from baseline 9% vs 2%; 95% CI 0.01–14.52; p = 0.0496) .
Improvements in pain interference, physical function mobility, fatigue, and HRQoL may be explained by the mechanism of action of burosumab. Burosumab addresses the deficiency of serum phosphate by directly binding to FGF23 and inhibiting its signaling, increasing tubular phosphate reabsorption, as well as increasing serum 1,25(OH)2D levels and increasing gastrointestinal phosphate absorption . Increased serum phosphate levels result in improved bone mineralization , improved muscular function , and restoration of ATP synthesis [31,32,33], and thus ultimately may manifest as improvements in patient-reported symptoms, function, and HRQoL.
In relation to PRO measurements, this trial has several limitations. Our trial was not powered to assess between-group differences for secondary and exploratory outcomes, such as PROs, nor for subgroup analyses. For example, sample size was insufficient to explore whether higher phosphate concentration or rapidity of correction of alkaline phosphatase reflected PRO measurements. Therefore, it remains unknown whether mid-range serum phosphate levels improve PROs to a greater extent than low-normal values. Children aged younger than 1 year or older than 12 years were not recruited, and children younger than 5 years did not complete PROs, precluding extrapolation of results to these age groups and limiting the sample size to 15 patients in the burosumab group and 20 patients in the conventional therapy group. Further, only those with RSS ≥ 2 were enrolled in this trial; thus, the baseline PRO scores or the degree of expected improvement with treatment for those with lower RSS scores is not known. This trial only randomized treatment for 64 weeks, while XLH is a lifelong chronic disease. Further follow-up is warranted to determine longer-term effects on HRQoL and patient-reported pain interference, physical function mobility, and fatigue. Furthermore, compared with the prior clinical standard of care, children on conventional treatment in this trial were perhaps more meticulously monitored and managed, because of the frequent visits and rigorous trial requirements. High levels of compliance and adherence to conventional treatment in clinical trial settings can result in greater improvements in outcomes with conventional therapy than that seen in routine standard of care [34,35,36,37].
In conclusion, in this phase 3 trial, changing from conventional therapy to burosumab was associated with numerical increases in PROMIS physical function mobility, clinically meaningful reductions in PROMIS pain interference and fatigue up to 64 weeks, and a statistically significant reduction in PROMIS pain interference up to 40 weeks. Statistically significant improvements in SF-10 PHS-10 were observed up to 64 weeks from baseline in children aged 5–12 years with XLH.
The corresponding author had full access to all the data in the study.
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We thank the clinical nurse coordinators at our sites, who ensured that the questionnaires were completed by patients or their caregivers. Medical writing and editorial support were provided by OPEN Health Medical Communications, with funding provided by Kyowa Kirin International. LMW is supported by a University of Ottawa Research Chair Award.
This study was funded by Kyowa Kirin International.
Conflict of interest
The following authors served as clinical investigators for one or more studies, including this trial, sponsored by Ultragenyx Pharmaceutical Inc. in partnership with Kyowa Kirin International plc: RP, MPW, FHG, CFM, LMW, ON, AAP, JHS, NN, HIC, PP, ES, WH, KM, HT, GSG, AB, FP, and EAI. AAP, NN, FP, and EAI have also received honoraria for serving as advisory board members or for lectures from Ultragenyx Pharmaceutical Inc. RP has received personal fees from Ultragenyx Pharmaceutical Inc. and Kyowa Kirin International plc, a research grant, consultation fees, honoraria, and travel grants from Kyowa Kirin International plc and Alexion UK, and non-financial support from Kyowa Kirin International plc. MPW has received research grant support, honoraria, and travel from Alexion Pharmaceutical Inc. FHG has received personal fees from Kyowa Kirin International plc and research funding from Amgen and Mereo BioPharma. LMW has served as a consultant to Ultragenyx, with funds to LMW’s institution. NN has received personal fees and non-financial support from Kyowa Kirin International plc and Ultragenyx Pharmaceutical Inc. during the conduct of the study, and personal fees and non-financial support (honoraria, consulting fees, and travel support) from Alexion UK outside the submitted work. PP has received research funding from Ultragenyx Pharmaceutical Inc. and is currently an employee of Ascendis Pharma Inc. WH has received honoraria, consulting fees, and travel support from Ultragenyx Pharmaceutical Inc. and research funding, honoraria, and travel support from Kyowa Kirin. GSG has received consulting fees from Ultragenyx Pharmaceutical Inc. AW and WS are employees of Kyowa Kirin International plc. AN is an employee of Chilli Consultancy and has received consultancy fees from Kyowa Kirin International plc to support the development of this manuscript. AC and AS are employees and stockholders of Ultragenyx Pharmaceutical Inc.
Human and Animal Rights and Informed Consent
The study was conducted in accordance with the Declaration of Helsinki and the Good Clinical Practice guidelines developed at the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use. Parents or guardians provided written informed consent for their children to participate, and children gave written assent according to local guidelines.
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Padidela, R., Whyte, M.P., Glorieux, F.H. et al. Patient-Reported Outcomes from a Randomized, Active-Controlled, Open-Label, Phase 3 Trial of Burosumab Versus Conventional Therapy in Children with X-Linked Hypophosphatemia. Calcif Tissue Int 108, 622–633 (2021). https://doi.org/10.1007/s00223-020-00797-x
- X-linked hypophosphatemia
- Patient-reported outcomes
- Patient-reported outcomes measurement information system