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NCT05966688 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Effect of Co-administration on the Pharmacokinetics of SPR720, Azithromycin, and Ethambutol in Healthy Participants

A Phase 1 study of Healthy Volunteers, sponsored by Spero Therapeutics.

Completed
Registry status
Phase 1
Development phase
39
Enrollment target
1
Study location

NCT05966688 is a Phase 1 study of Healthy Volunteers that has completed, run by Spero Therapeutics. The registered enrollment target is 39 participants, below the 482-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05966688, a Phase 1 study of Healthy Volunteers, has completed, sponsored by Spero Therapeutics.

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

Study Summary

The primary purpose of this study is to evaluate the pharmacokinetics (PK) of SPR720, azithromycin, and ethambutol, administered separately and co-administered, in healthy adult participants.

Conditions Studied

Interventions

  • DRUG Azithromycin
  • DRUG Ethambutol
  • DRUG SPR720

Study Locations (1)

Ohio

  • Medpace Clinical Pharmacology Unit - Cincinnati

Trial Details

FieldValue
Enrollment Target 39 participants
Start Date 2023-08-04
Est. Completion 2024-02-04
Phase Phase 1

Sponsor

Spero Therapeutics

14 total trials

What the Registry Record Tells You About NCT05966688

The ClinicalTrials.gov registry entry for NCT05966688 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 39 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 482-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (92% lower). The listed sponsor is Spero Therapeutics, which has 14 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy Volunteers appearing as the primary indexed condition, and to 3 interventions - of which Azithromycin is the first listed.

NCT05966688 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT05966688 about?

NCT05966688 is a clinical study titled "A Study to Evaluate the Effect of Co-administration on the Pharmacokinetics of SPR720, Azithromycin, and Ethambutol in Healthy Participants". The primary purpose of this study is to evaluate the pharmacokinetics (PK) of SPR720, azithromycin, and ethambutol, administered separately and co-administered, in healthy adult participants.

What is the current status of trial NCT05966688?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 39 participants. The study started on 2023-08-04. Estimated completion is 2024-02-04.

What conditions does trial NCT05966688 study?

This clinical trial studies the following conditions: Healthy Volunteers.

What interventions are being tested in trial NCT05966688?

The interventions under investigation include: Azithromycin (DRUG), Ethambutol (DRUG), SPR720 (DRUG).

Who is sponsoring clinical trial NCT05966688?

This trial is sponsored by Spero Therapeutics, which has 14 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05966688 being conducted?

This trial has 1 study location across Ohio. 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.