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NCT03998176 · ClinicalTrials.gov registry record · Phase 4

Bictegravir/Emtricitabine/Tenofovir Alafenamide (B/F/TAF) in HIV-1 Infected Patients With Active Illicit Substance usE

A Phase 4 study, sponsored by University of Nebraska.

Completed
Registry status
Phase 4
Development phase
43
Enrollment target

NCT03998176: Completed Phase 4 study, sponsored by University of Nebraska.

NCT03998176 is a Phase 4 study that has completed, run by University of Nebraska. The registered enrollment target is 43 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03998176, a Phase 4 study, has completed, sponsored by University of Nebraska.

COMPLETED
Registry status
Phase 4
Development phase
43 participants
Enrollment target

Study Summary

This study will evaluate the efficacy and safety of bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) in HIV-1 infected patients who actively use illicit substances. The study will also evaluate retention in care and adherence to B/F/TAF by self-report and pharmacokinetic analysis.

Primary Outcome

The percentage of participants achieving HIV-1 RNA \< 50 copies/mL at Week 24 analyzed by the snapshot algorithm, which defines a participants virologic response status using only the viral load at the predefined time point within an allowed window of time, along with study drug discontinuation status.

Interventions

  • DRUG Bictegravir/emtricitabine/tenofovir alafenamide

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2019-10-09
Est. Completion 2022-04-01
Phase Phase 4
University of Nebraska

407 total trials

What the finished NCT03998176 record still lists

NCT03998176 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which Bictegravir/emtricitabine/tenofovir alafenamide is the first listed.

NCT03998176 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03998176 about?

NCT03998176 is a clinical study titled "Bictegravir/Emtricitabine/Tenofovir Alafenamide (B/F/TAF) in HIV-1 Infected Patients With Active Illicit Substance usE". This study will evaluate the efficacy and safety of bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) in HIV-1 infected patients who actively use illicit substances. The study will also evaluate retention in care and adherence to B/F/TAF by self-report and pharmacokinetic analysis.

What is the current status of trial NCT03998176?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 43 participants. The study started on 2019-10-09. Estimated completion is 2022-04-01.

What interventions are being tested in trial NCT03998176?

The interventions under investigation include: Bictegravir/emtricitabine/tenofovir alafenamide (DRUG).

Who is sponsoring clinical trial NCT03998176?

This trial is sponsored by University of Nebraska, which has 407 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03998176's enrollment target sits among peer trials

43 1371st of 2000 higher than 621 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT03998176, the US trial registry maintained by the National Library of Medicine. NCT03998176 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.