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NCT06406348 · ClinicalTrials.gov registry record · Phase 1

A Phase 1 Trial to Assess Safety, Tolerability and Pharmacokinetics of ALIA-1758 in Healthy Participants

A Phase 1 study, sponsored by AbbVie.

Completed
Registry status
Phase 1
Development phase
53
Enrollment target

NCT06406348: Completed Phase 1 study, sponsored by AbbVie.

NCT06406348 is a Phase 1 study that has completed, run by AbbVie. The registered enrollment target is 53 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (12% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06406348, a Phase 1 study, has completed, sponsored by AbbVie.

COMPLETED
Registry status
Phase 1
Development phase
53 participants
Enrollment target

Study Summary

This is a Phase 1, first in human (FIH), double-blind, placebo-controlled, single ascending dose (SAD) trial to assess the safety, tolerability, and pharmacokinetics (PK) of intravenously (IV) or subcutaneously (SC) injected ALIA-1758 in healthy male and female participants.

Primary Outcome

Incidence, severity, seriousness, and causality of treatment-emergent adverse events (TEAEs)

Interventions

  • OTHER Placebo
  • DRUG ALIA-1758

Trial Details

FieldValue
Enrollment Target 53 participants
Start Date 2024-05-09
Est. Completion 2025-04-22
Phase Phase 1
AbbVie

526 total trials

What the finished NCT06406348 record still lists

NCT06406348 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 53 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (12% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT06406348 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06406348 about?

NCT06406348 is a clinical study titled "A Phase 1 Trial to Assess Safety, Tolerability and Pharmacokinetics of ALIA-1758 in Healthy Participants". This is a Phase 1, first in human (FIH), double-blind, placebo-controlled, single ascending dose (SAD) trial to assess the safety, tolerability, and pharmacokinetics (PK) of intravenously (IV) or subcutaneously (SC) injected ALIA-1758 in healthy male and female participants.

What is the current status of trial NCT06406348?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 53 participants. The study started on 2024-05-09. Estimated completion is 2025-04-22.

What interventions are being tested in trial NCT06406348?

The interventions under investigation include: Placebo (OTHER), ALIA-1758 (DRUG).

Who is sponsoring clinical trial NCT06406348?

This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06406348's enrollment target sits among peer trials

53 948th of 2000 higher than 1,045 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT06406348, the US trial registry maintained by the National Library of Medicine. NCT06406348 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.