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8– 10 The objective of this post hoc analysis was to evaluate the variability in pancreatic enzyme concentrations in type 2 diabetic and obese nondiabetic (control) populations.
The objective of this post hoc analysis was to examine the efficacy and safety of ULT with febuxostat or allopurinol in a subset of elderly subjects enrolled in the CONFIRMS trial.
The objective of this post hoc analysis was to evaluate the efficacy and safety of pregabalin in older patients with neuropathic pain using pooled double-blind, randomized, placebo-controlled studies of pregabalin in patients with DPN or PHN.
The objective of this post hoc analysis was to examine the efficacy and safety profile of LDX by sex and age group in children with ADHD in a laboratory school setting.
The objective of this post hoc analysis was to assess the influence of seasonality on bleeding frequency and patient-assessed pain in these patients with haemophilia B receiving on-demand therapy.
The objective of this post hoc subgroup analysis described herein was to identify a "better efficacy" patient population within VELOUR study that may have derived greater clinical benefit from treatment with FOLFIRI plus aflibercept.
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The objective of this post-hoc analysis was to compare the demographics and clinical features of patients with normal PAP, borderline mPAP (BoPAP), and elevated PAP (PAH) in a large international cohort of patients with SSc who participated in the DETECT study.
The objective of this post-hoc exploratory analysis was to evaluate the frequency of cognitive impairment in patients with FMS using a brief and widely used quantitative measure of the cognitive status in adults such as the Mini Mental State Examination.
In a context of ageing of the older European population, the objectives of this post hoc analysis of the data collected during the ARIZONA study was to determine whether, beyond 70 years, age remained a risk factor for PHN and increased the burden of the disease, and whether a new age threshold could be defined in the most elderly patients.
3 The objectives of this post hoc analysis were to assess: 1) changes in serum calcium in patients with high serum PINP (>200 μg/L) at any time point during the study; and 2) changes in serum PINP and serum calcium in patients with calcium metabolism-related adverse events (AEs) during the study.
The objectives of this post-hoc 48-week GAM analysis were to assess exposure response relationship and other possible predictive factors, as before.
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