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NCT03284164 · ClinicalTrials.gov registry record · Phase 1

Evaluation of Effect of Renal Impairment on the PK of Tenofovir Exalidex

A Phase 1 study of Renal Impairment, sponsored by ContraVir Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
16
Enrollment target
1
Study location

NCT03284164: Completed Phase 1 study of Renal Impairment, sponsored by ContraVir Pharmaceuticals.

NCT03284164 is a Phase 1 study of Renal Impairment that has completed, run by ContraVir Pharmaceuticals. The registered enrollment target is 16 participants, below the 34-participant average among 32 other Renal Impairment trials with a reported enrollment target (53% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03284164, a Phase 1 study of Renal Impairment, has completed, sponsored by ContraVir Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
16 participants
Enrollment target
1
Study location

Study Summary

This is a Phase 1 study to investigate the effects of Renal Impairment on the pharmacokinetics of Tenofovir exalidex

Primary Outcome

Measuring Cmax : the peak plasma concentration

Conditions Studied

Interventions

  • DRUG Tenofovir Exalidex (TXL)

Study Locations (1)

Florida

  • Orlando Clinical Research Center - Orlando

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2017-09-28
Est. Completion 2018-02-20
Phase Phase 1
ContraVir Pharmaceuticals

2 total trials

What the finished NCT03284164 record still lists

NCT03284164 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 34-participant average among 32 other Renal Impairment trials with a reported enrollment target (53% lower).

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

NCT03284164 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT03284164 about?

NCT03284164 is a clinical study titled "Evaluation of Effect of Renal Impairment on the PK of Tenofovir Exalidex". This is a Phase 1 study to investigate the effects of Renal Impairment on the pharmacokinetics of Tenofovir exalidex

What is the current status of trial NCT03284164?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2017-09-28. Estimated completion is 2018-02-20.

What conditions does trial NCT03284164 study?

This clinical trial studies the following conditions: Renal Impairment.

What interventions are being tested in trial NCT03284164?

The interventions under investigation include: Tenofovir Exalidex (TXL) (DRUG).

Who is sponsoring clinical trial NCT03284164?

This trial is sponsored by ContraVir Pharmaceuticals, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03284164 being conducted?

This trial has 1 study location 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 NCT03284164's enrollment target sits among peer trials

16 28th of 32 higher than 2 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 NCT03284164, the US trial registry maintained by the National Library of Medicine. NCT03284164 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.