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NCT02191098 · ClinicalTrials.gov registry record · Phase 1

Proof of Principle Study of Pulse Dosing of IL-15 to Deplete the Reservoir in HIV Infected People

A Phase 1 study of HIV and Stable ART, sponsored by University of Minnesota.

Completed
Registry status
Phase 1
Development phase
10
Enrollment target
1
Study location

NCT02191098: Completed Phase 1 study of HIV and Stable ART, sponsored by University of Minnesota.

NCT02191098 is a Phase 1 study of HIV and Stable ART that has completed, run by University of Minnesota. The registered enrollment target is 10 participants, below the 440-participant average among 303 other HIV trials with a reported enrollment target (98% 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

NCT02191098, a Phase 1 study of HIV and Stable ART, has completed, sponsored by University of Minnesota.

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

Study Summary

To assess the safety and tolerability of ALT-803, as well as, the potential efficacy of ALT-803 in HIV

Primary Outcome

Safety and tolerability is determined by the incidence of adverse events, size of the inducible reservoir as estimated using the TILDA assay

Conditions Studied

Interventions

  • DRUG ALT-803

Study Locations (1)

Minnesota

  • University of Minnesota - Minneapolis

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2015-06
Est. Completion 2019-09-09
Phase Phase 1
University of Minnesota

966 total trials

What the finished NCT02191098 record still lists

NCT02191098 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 440-participant average among 303 other HIV trials with a reported enrollment target (98% lower).

The record links to 2 conditions, with HIV appearing as the primary indexed condition, and to 1 intervention - of which ALT-803 is the first listed.

NCT02191098 reports a single indexed study location in Minnesota.

Frequently Asked Questions

What is clinical trial NCT02191098 about?

NCT02191098 is a clinical study titled "Proof of Principle Study of Pulse Dosing of IL-15 to Deplete the Reservoir in HIV Infected People". To assess the safety and tolerability of ALT-803, as well as, the potential efficacy of ALT-803 in HIV

What is the current status of trial NCT02191098?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 10 participants. The study started on 2015-06. Estimated completion is 2019-09-09.

What conditions does trial NCT02191098 study?

This clinical trial studies the following conditions: HIV, Stable ART.

What interventions are being tested in trial NCT02191098?

The interventions under investigation include: ALT-803 (DRUG).

Who is sponsoring clinical trial NCT02191098?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02191098 being conducted?

This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for HIV

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 NCT02191098's enrollment target sits among peer trials

10 298th of 303 higher than 5 of 303 other HIV trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other HIV 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 NCT02191098, the US trial registry maintained by the National Library of Medicine. NCT02191098 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.