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NCT05216354 · ClinicalTrials.gov registry record · Phase 1

Fruquintinib Renal Impairment Study

A Phase 1 study of Renal Impairment, sponsored by Hutchmed.

Completed
Registry status
Phase 1
Development phase
24
Enrollment target
2
Study locations

NCT05216354: Completed Phase 1 study of Renal Impairment, sponsored by Hutchmed.

NCT05216354 is a Phase 1 study of Renal Impairment that has completed, run by Hutchmed. The registered enrollment target is 24 participants, below the 34-participant average among 32 other Renal Impairment trials with a reported enrollment target (29% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05216354, a Phase 1 study of Renal Impairment, has completed, sponsored by Hutchmed.

COMPLETED
Registry status
Phase 1
Development phase
24 participants
Enrollment target
2
Study locations

Study Summary

A multicenter, open label, single-dose, single-period, sequential study to assess the effect of renal impairment on the pharmacokinetics of Fruquintinib

Primary Outcome

Area under the plasma concentration-time curve from time 0 to time of the last measurable concentration

Conditions Studied

Interventions

  • DRUG Fruquintinib

Study Locations (2)

Florida

  • Clinical Pharmacology of Miami - Miami
  • Orlando Clinical Research Center - Orlando

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2022-03-11
Est. Completion 2023-06-26
Phase Phase 1
Hutchmed

17 total trials

What the finished NCT05216354 record still lists

NCT05216354 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 34-participant average among 32 other Renal Impairment trials with a reported enrollment target (29% lower).

The record links to 1 condition, with Renal Impairment appearing as the primary indexed condition, and to 1 intervention - of which Fruquintinib is the first listed.

NCT05216354 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT05216354 about?

NCT05216354 is a clinical study titled "Fruquintinib Renal Impairment Study". A multicenter, open label, single-dose, single-period, sequential study to assess the effect of renal impairment on the pharmacokinetics of Fruquintinib

What is the current status of trial NCT05216354?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2022-03-11. Estimated completion is 2023-06-26.

What conditions does trial NCT05216354 study?

This clinical trial studies the following conditions: Renal Impairment.

What interventions are being tested in trial NCT05216354?

The interventions under investigation include: Fruquintinib (DRUG).

Who is sponsoring clinical trial NCT05216354?

This trial is sponsored by Hutchmed, which has 17 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05216354 being conducted?

This trial has 2 study locations across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Renal Impairment

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05216354's enrollment target sits among peer trials

24 23rd of 32 higher than 9 of 32 other Renal Impairment trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Renal Impairment trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05216354, the US trial registry maintained by the National Library of Medicine. NCT05216354 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.