ClinicalTrials.gg
RecruitingNCT07227922RENALUpdated Dec 23, 2025

Clofutriben Pharmacokinetics in Patients With Impaired Renal Function

A Phase 1 interventional study of 12mg clofutriben in Moderate Renal Impairment, sponsored by Sparrow Pharmaceuticals. Recruiting at 1 site in United States. Open to participants aged 18 Years to 83 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-12-23.

Sponsored by Sparrow Pharmaceuticals · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Apr 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started Nov 2025; still recruiting 11 months later.
Phase
Phase 1
Study type
Interventional
Enrollment
16
Allocation
Not applicable
Ages
18 Years to 83 Years
Sex
All
01

Study summary

This is a Phase 1, single-center, open-label, single-dose trial. Sixteen participants are planned: 8 participants with moderate renal impairment and 8 matched control participants with normal renal function.

Read the detailed description

Following Screening, enrolled participants will be confined to a clinical research unit for 6 days. Each participant will receive a single oral dose of clofutriben. Clofutriben PK, safety, and tolerability will be assessed. The participants will be contacted by telephone 4 weeks after clofutriben administration for safety follow-up.

02

Conditions studied

  • Moderate Renal Impairment

Keywords

  • Renal
03

In context

Lead sponsor

Sparrow Pharmaceuticals is the lead sponsor of 8 studies on the registry; 2 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

04

Who can participate

Ages eligible
18 Years to 83 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Male and female participants with stable moderate renal impairment (estimated [eGFR]: 30 to \<60 mL/min) and matched (by sex, age, and weight) control participants with normal renal function (eGFR: ≥90 mL/min) will be enrolled in this trial.

Exclusion criteria

Exclusion Criteria:

  • Participant whose current or recent medical conditions, medications, or procedures could increase participant's safety risk, or whom the Investigator considers not suitable for entry into the trial or the participant, or who has abnormal 12-lead (ECG)/ vital sign measurements/ laboratory test results at Screening and Check-in, will not be enrolled
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
16 participants (estimated)

Study arms

  • Experimental
    clofutriben

    Drug: 12mg clofutriben

Interventions

  • Each participant will receive a single oral dose of clofutriben

06

What researchers measure

Primary outcomes

  1. 1. Maximum plasma concentration (Cmax)

    Conclusions that clofutriben and AS2570469 exposures (separately) are not altered by moderate renal impairment will be reached if the 95% CIs of the geometric mean estimates of AUC0-t, AUC0-inf, and Cmax of clofutriben and AS2570469 fall within the \[60%, 140%\] range.

    Time frame: from enrollment through treatment for 6 days.

  2. 2. Area under the plasma time-concentration curve (AUC0-t, AUC0-inf)

    Conclusions that clofutriben and AS2570469 exposures (separately) are not altered by moderate renal impairment will be reached if the 95% CIs of the geometric mean estimates of AUC0-t, AUC0-inf, and Cmax of clofutriben and AS2570469 fall within the \[60%, 140%\] range.

    Time frame: from enrollment through treatment for 6 days.

07

Study locations

1 of 1 sites recruiting
  • Orlando Clinical Research Center
    Orlando, Florida 32809, United States
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 23, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07227922
Lead sponsor
Sparrow Pharmaceuticals
Responsible party
Sponsor
First posted
Nov 13, 2025
Start date
Nov 30, 2025
Primary completion
Apr 30, 2026 (estimated)
Completion
Jul 1, 2026 (estimated)
Last update
Dec 23, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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Discussion

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Studies of the drug tested here: ASP3662

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