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Active, not recruiting Phase 1 Interventional

Safety, Tolerability, and Efficacy of IL-15 Superagonist (N-803) With and Without Combination Broadly Neutralizing Antibodies to Induce HIV-1 Control During Analytic Treatment Interruption

ClinicalTrials.gov ID: NCT04340596

Public ClinicalTrials.gov record NCT04340596. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 7:35 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase I Clinical Trial of the Safety, Tolerability, and Efficacy of IL-15 Superagonist (N-803) With and Without Combination Broadly Neutralizing Antibodies to Induce HIV-1 Control During Analytic Treatment Interruption

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the safety, tolerability, and efficacy of N-803, an IL-15 superagonist, with or without combination broadly neutralizing antibodies (bNAbs), to induce HIV-1 control during analytic treatment interruption (ATI).

Study identification

NCT ID
NCT04340596
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1
Enrollment
118 participants

Conditions and interventions

Conditions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 21, 2021 (Actual)
Primary completion
May 7, 2026 (Actual)
Completion
Dec 30, 2026 (Estimated)
Last update posted
Aug 26, 2026

2021 – 2026

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
Alabama CRS (Site ID# 31788) Birmingham Alabama 35222 —
UCLA CARE Center CRS Los Angeles California 90035 —
UCSD Antiviral Research Center CRS (Site ID: 701) San Diego California 92103 —
University of California, San Fransisco HIV/AIDS CRS San Francisco California 94110 —
Whitman-Walker Institute, Inc. CRS (Site ID: 31791) Washington D.C. District of Columbia 20005 —
Northwestern University CRS Chicago Illinois 60611 —
Massachusetts General Hospital CRS (MGH CRS) (Site ID: 101) Boston Massachusetts 02114 —
Washington University Therapeutics (WT) CRS St Louis Missouri 63110-1010 —
New Jersey Medical School Clinical Research Center CRS [Site ID: 31786] Newark New Jersey 07103 —
Columbia P&S CRS New York New York 10032 —
Weill Cornell Uptown CRS (Site ID: 7803) New York New York 10065 —
Chapel Hill CRS (Site ID: 3201) Chapel Hill North Carolina 27599 —
Case Clinical Research Site Cleveland Ohio 44106 —
Penn Therapeutics, CRS (Site ID: 6201) Philadelphia Pennsylvania 19104 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04340596, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 26, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04340596 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →