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NCT05526911 · ClinicalTrials.gov registry record · Phase 1

A Phase 1, Drug-Drug Interaction Study of TBAJ-876 in Healthy Adults

A Phase 1 study of Tuberculosis and Pulmonary Disease, sponsored by Global Alliance for TB Drug Development.

Completed
Registry status
Phase 1
Development phase
28
Enrollment target
1
Study location

NCT05526911 is a Phase 1 study of Tuberculosis and Pulmonary Disease that has completed, run by Global Alliance for TB Drug Development. The registered enrollment target is 28 participants, below the 933-participant average among 29 other Tuberculosis trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05526911, a Phase 1 study of Tuberculosis and Pulmonary Disease, has completed, sponsored by Global Alliance for TB Drug Development.

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

Study Summary

A Phase 1, Drug-Drug Interaction Study to Evaluate the Safety, Tolerability, and the Induction Potential of TBAJ-876 on CYP3A4 and P-glycoprotein and the Inhibition Potential of TBAJ-876 on P-glycoprotein in Healthy Adult Subjects

Interventions

  • DRUG Midazolam
  • DRUG Digoxin
  • DRUG TBAJ-876

Study Locations (1)

New Jersey

  • TKL Research, Inc. - Fair Lawn

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2022-06-30
Est. Completion 2022-09-26
Phase Phase 1

What the Registry Record Tells You About NCT05526911

The ClinicalTrials.gov registry entry for NCT05526911 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 28 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 933-participant average among 29 other Tuberculosis trials with a reported enrollment target (97% lower). The listed sponsor is Global Alliance for TB Drug Development, which has 13 total studies on file at ClinicalTrials.gov.

The record links to 7 conditions, with Tuberculosis appearing as the primary indexed condition, and to 3 interventions - of which Midazolam is the first listed.

NCT05526911 reports 1 study location spanning 1 distinct geographic area - top geographies include New Jersey.

Frequently Asked Questions

What is clinical trial NCT05526911 about?

NCT05526911 is a clinical study titled "A Phase 1, Drug-Drug Interaction Study of TBAJ-876 in Healthy Adults". A Phase 1, Drug-Drug Interaction Study to Evaluate the Safety, Tolerability, and the Induction Potential of TBAJ-876 on CYP3A4 and P-glycoprotein and the Inhibition Potential of TBAJ-876 on P-glycoprotein in Healthy Adult Subjects

What is the current status of trial NCT05526911?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2022-06-30. Estimated completion is 2022-09-26.

What conditions does trial NCT05526911 study?

This clinical trial studies the following conditions: Tuberculosis, Pulmonary Disease, Tuberculosis, Pulmonary, Multi-drug Resistant Tuberculosis, Drug Sensitive Tuberculosis.

What interventions are being tested in trial NCT05526911?

The interventions under investigation include: Midazolam (DRUG), Digoxin (DRUG), TBAJ-876 (DRUG).

Who is sponsoring clinical trial NCT05526911?

This trial is sponsored by Global Alliance for TB Drug Development, which has 13 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05526911 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.