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CompletedNCT02752633Updated Apr 9, 2024Results posted

Effect of Allopurinol and Febuxostat on Urinary 2,8-Dihydroxyadenine Excretion

A Phase 4 interventional study of Allopurinol and Febuxostat in Adenine Phosphoribosyltransferase Deficiency, sponsored by Landspitali University Hospital. Completed at 1 site in Iceland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-04-09.

Sponsored by Landspitali University Hospital · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
9
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study summary

This exploratory pilot study was an open-label, crossover, single-center and non-randomized clinical trial designed to compare the effect of the standardly employed doses of allopurinol (400 mg/day) and febuxostat (80 mg/day) on the urinary 2,8-dihydroxyadenine (DHA) excretion in patients with adenine phosphoribosyltransferase (APRT) deficiency.

Read the detailed description

This exploratory pilot study was an open-label, crossover, single-center and non-randomized clinical trial designed to compare the effect of the standardly employed doses of allopurinol (400 mg/day) and febuxostat (80 mg/day) on the urinary DHA excretion in patients with APRT deficiency. The study was conducted between May 2013 and May 2015 as participants were enrolled at different times. The only study site was Landspitali - The National University Hospital of Iceland in Reykjavik, Iceland. The Data (Observational) Safety Monitoring Board (D/OSMB) constituted by the National Institutes of Health had oversight responsibility of the Data Safety Monitoring Plan for this clinical trial. The monitoring board reviewed accrual, patterns and frequencies of all adverse events, and protocol compliance every 6-12 months. All study subjects gave a written informed consent for their participation.

Study participants were recruited from a group of patients with confirmed APRT deficiency enrolled in the National Institutes of Health supported APRT Deficiency Registry of the Rare Kidney Stone Consortium (RKSC, http://www.rarekidneystones.org/). Confirmation of APRT deficiency was based upon the determination of known biallelic pathogenic APRT mutations or absent APRT enzyme activity. Participants were eligible for inclusion if they a) were currently receiving allopurinol therapy (the currently recommended treatment for patients with APRT deficiency); b) were willing to interrupt their allopurinol treatment for a total of 3 weeks as outlined below and c) were at least 18 years of age. There were no other exclusion criteria if the above inclusions criteria were met.

Study interventions After a 7-day washout period, all consenting subjects were prescribed 400 mg of allopurinol in a single daily dose for 14 days. After a second 7-day washout period, all subjects were prescribed 80 mg febuxostat in a single daily dose for another 14 days. Twenty-four hour and first morning urine samples were collected at the end of the first washout period, and at the end of allopurinol and febuxostat treatment periods, respectively (days 7, 21 and 42). To minimize the potential adverse effect of dietary purine intake on the results, participants were asked to keep a food record while they collected the first 24 hr urine sample and adhere to the same diet when they collected the other two 24 hr urine samples. No further measures were taken to control dietary purine intake during the study period. At the end of the study, all patients were advised to return to their regular allopurinol dosing regimens.

Measurements Urinary DHA was measured using a rapid and robust ultra high power liquid chromatography - electrospray tandem mass spectrometry (UPLC-MS/MS)), recently developed by our group. The 24-hour urinary DHA excretion (mg/24-hours) was measured and the urinary DHA-to-creatinine ratio (mg/mmol) in first morning urine samples was calculated. Urine and serum creatinine concentrations were measured with an isotope dilution mass spectrometry (IDMS) standardized laboratory method.

Outcome measures The primary trial endpoint is the 24 hr urinary DHA excretion and in patients taking the two study drugs, allopurinol (daily dose 400 mg) and febuxostat (daily dose 80 mg), evaluated at the conclusion of each 14 day drug treatment period.

Statistical Analysis Data are presented as urinary DHA excretion (mg/day) for timed collections and urinary DHA-to-creatinine ratio in first morning urine samples. Data for the whole group are presented as a median (range). Differences in the median urinary DHA excretion and the urinary DHA-to-creatinine ratio, off pharmacotherapy and on the two study drugs, febuxostat and allopurinol, were compared with a paired t-test.

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Conditions studied

  • Adenine Phosphoribosyltransferase Deficiency

Keywords

  • Xanthine dehydrogenase inhibitor treatment, pharmacotherapy
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In context

Lead sponsor

Landspitali University Hospital is the lead sponsor of 20 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • All patients 18 year and older who are enrolled in the APRT Deficiency Registry of The Rare Kidney Stone Consortium.

Exclusion criteria

Exclusion Criteria:

  • Patients do not want to interrupt drug (allopurinol) treatment for a total of two weeks as requested in protocol. No other exclusion criteria if inclusion criteria are met.
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Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
9 participants (actual)

Study arms

  • Experimental
    Study subjects

    Following a 7 day washout period all patients receive allopurinol (400 mg/day) as a single daily dose for 2 weeks. Following another 7 day washout period all participants receive febuxostat, 80 mg/day as a single daily dose, for 2 weeks.

    Drug: Allopurinol · Drug: Febuxostat

Interventions

  • DrugAllopurinol

    This is a clinical trial comparing the effect of 80 mg/day of febuxostat to 400 mg/day of allopurinol on the urinary excretion of 2,8-dihydroxyadenine in patients with APRT deficiency.

    Also known as: Apurin, ATC Code M04AA01

  • DrugFebuxostat

    This is a clinical trial comparing the effect of 80 mg/day of febuxostat to 400 mg/day of allopurinol on the urinary excretion of 2,8-dihydroxyadenine in patients with APRT deficiency.

    Also known as: Uloric, ATC Code M04AA03

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What researchers measure

Primary outcomes

  1. Urinary 2,8-dihydroxyadenine Excretion

    Time frame: 7, 21 and 42 days

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Results

Posted Dec 27, 2017

Participant flow

Participant flow — Overall Study
MilestoneAllopurinol/Febuxostat Treatment
Started9
Completed8
Not completed1
Withdrew: Withdrawal by subject1

Outcome measures

PrimaryUrinary 2,8-dihydroxyadenine Excretion
Time frame:
7, 21 and 42 days
Reported as:
Median · mg/24-h
Urinary 2,8-dihydroxyadenine Excretion
mg/24-hAllopurinol/Febuxostat Treatment
Baseline116 (75 to 289)
On allopurinol treatment45 (13 to 112)
On febuxostat treatment13 (10 to 13)
Statistical analysis
  • Allopurinol/Febuxostat Treatment · Wilcoxon (Mann-Whitney) · p = <.05

Adverse events

Collected over Throughout the study, 42 days.. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Allopurinol/Febuxostat Treatment0/9 (0%)0/9 (0%)0/9 (0%)

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Allopurinol/Febuxostat Treatment
<=18 years0
Between 18 and 65 years8
>=65 years1
Age, Continuous
Age, Continuous(years)Allopurinol/Febuxostat Treatment
Median54 (28 to 67)
Sex: Female, Male
Sex: Female, Male(Participants)Allopurinol/Febuxostat Treatment
Female5
Male4
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Allopurinol/Febuxostat Treatment
Race — American Indian or Alaska Native0
Race — Asian0
Race — Native Hawaiian or Other Pacific Islander0
Race — Black or African American0
Race — White9
Race — More than one race0
Race — Unknown or Not Reported0
Region of Enrollment
Region of Enrollment(participants)Allopurinol/Febuxostat Treatment
Iceland9
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Study locations

1 site
  • Landspitali - The National University Hospital of Iceland
    Reykjavik, 101, Iceland
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References and documents

Publications

  • Runolfsdottir HL, Palsson R, Agustsdottir IM, Indridason OS, Edvardsson VO. Kidney Disease in Adenine Phosphoribosyltransferase Deficiency. Am J Kidney Dis. 2016 Mar;67(3):431-8. doi: 10.1053/j.ajkd.2015.10.023. Epub 2015 Dec 25. PubMed 26724837 ↗

Individual participant data

Plan to share: Yes — Published in Eur J Intern Med. 2017 Dec 11, 2017. PMID: 29241594 DOI: 10.1016/j.ejim.2017.10.007

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 9, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02752633
Lead sponsor
Landspitali University Hospital
Collaborators
Mayo Clinic, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Responsible party
Sponsor
First posted
Apr 27, 2016
Start date
May 2013
Primary completion
May 2015
Completion
May 2015
Results posted
Dec 27, 2017
Last update
Apr 9, 2024

Study contacts

Vidar O Edvardsson, MD
principal investigator · Landspitali - The National University Hospital of Iceland, Reykjavik

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2017. You cannot join it, but the record below documents what was studied.

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