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NCT07146750 · ClinicalTrials.gov registry record · Phase 1

A Bioequivalence Study of Amlitelimab Delivered by 2 Different Devices in Healthy Adult Participants

A Phase 1 study of Healthy Volunteers, sponsored by Sanofi.

Active
Registry status
Phase 1
Development phase
212
Enrollment target
1
Study location

NCT07146750 is a Phase 1 study of Healthy Volunteers that is active but no longer recruiting, run by Sanofi. The registered enrollment target is 212 participants, below the 481-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (56% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07146750, a Phase 1 study of Healthy Volunteers, is active but no longer recruiting, sponsored by Sanofi.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
212 participants
Enrollment target
1
Study location

Study Summary

This is a single-center, open-label, randomized, single-dose, parallel, Phase 1, 4-arm study designed to determine the bioequivalence and investigate the safety and tolerability profiles of subcutaneous amlitelimab delivered by 2 different devices at 2 different total doses in healthy adult participants.

Conditions Studied

Interventions

  • COMBINATION_PRODUCT SAR445229

Study Locations (1)

Florida

  • Clinical Pharmacology of Miami- Site Number : 8400001 - Miami

Trial Details

FieldValue
Enrollment Target 212 participants
Start Date 2025-08-25
Est. Completion 2026-04-08
Phase Phase 1

Sponsor

Sanofi

713 total trials

What the Registry Record Tells You About NCT07146750

The ClinicalTrials.gov registry entry for NCT07146750 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 212 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 481-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (56% lower). The listed sponsor is Sanofi, which has 713 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy Volunteers appearing as the primary indexed condition, and to 1 intervention - of which SAR445229 is the first listed.

NCT07146750 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.

Frequently Asked Questions

What is clinical trial NCT07146750 about?

NCT07146750 is a clinical study titled "A Bioequivalence Study of Amlitelimab Delivered by 2 Different Devices in Healthy Adult Participants". This is a single-center, open-label, randomized, single-dose, parallel, Phase 1, 4-arm study designed to determine the bioequivalence and investigate the safety and tolerability profiles of subcutaneous amlitelimab delivered by 2 different devices at 2 different total doses in healthy adult particip...

What is the current status of trial NCT07146750?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 212 participants. The study started on 2025-08-25. Estimated completion is 2026-04-08.

What conditions does trial NCT07146750 study?

This clinical trial studies the following conditions: Healthy Volunteers.

What interventions are being tested in trial NCT07146750?

The interventions under investigation include: SAR445229 (COMBINATION_PRODUCT).

Who is sponsoring clinical trial NCT07146750?

This trial is sponsored by Sanofi, which has 713 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07146750 being conducted?

This trial has 1 study location across Florida. 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.