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NCT06982352 · ClinicalTrials.gov registry record · Phase 1

Safety and Pharmacokinetics of LPX-TI641 in Atopic Dermatitis and Psoriasis

A Phase 1 study of Atopic Dermatitis (AD) and Psoriasis (PsO), sponsored by LAPIX Therapeutics.

Recruiting
Registry status
Phase 1
Development phase
48
Enrollment target
3
Study locations

NCT06982352 is a Phase 1 study of Atopic Dermatitis (AD) and Psoriasis (PsO) that is actively recruiting participants, run by LAPIX Therapeutics. The registered enrollment target is 48 participants, below the 104-participant average among 7 other Atopic Dermatitis (AD) trials with a reported enrollment target (54% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT06982352, a Phase 1 study of Atopic Dermatitis (AD) and Psoriasis (PsO), is actively recruiting participants, sponsored by LAPIX Therapeutics.

RECRUITING
Registry status
Phase 1
Development phase
48 participants
Enrollment target
3
Study locations

Study Summary

The goal of this clinical trial is to study the drug LPX-TI641 in patients with atopic dermatitis and psoriasis. We will compare the safety and tolerability of LPX-TI641 to placebo ( a look-alike solution) that contains no drug. We will also evaluate the plasma pharmacokinetics of LPX-TI641. LPX-TI641 (or placebo) will be administered orally for 28 days.

Interventions

  • DRUG Placebo
  • DRUG LPX-TI641

Study Locations (3)

North Dakota

  • Red River Research Partners - Fargo

Texas

  • Clinical Investigations of Texas - Dallas

Jordan

  • Triumpharma Clinical Research Unit at AlEssra Hospital - Amman

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2025-06-15
Est. Completion 2026-04-15
Phase Phase 1

Sponsor

LAPIX Therapeutics

3 total trials

What the Registry Record Tells You About NCT06982352

The ClinicalTrials.gov registry entry for NCT06982352 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 48 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 104-participant average among 7 other Atopic Dermatitis (AD) trials with a reported enrollment target (54% lower). The listed sponsor is LAPIX Therapeutics, which has 3 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Atopic Dermatitis (AD) appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT06982352 reports 3 study locations spanning 3 distinct geographic areas - top geographies include North Dakota, Texas, Jordan.

Frequently Asked Questions

What is clinical trial NCT06982352 about?

NCT06982352 is a clinical study titled "Safety and Pharmacokinetics of LPX-TI641 in Atopic Dermatitis and Psoriasis". The goal of this clinical trial is to study the drug LPX-TI641 in patients with atopic dermatitis and psoriasis. We will compare the safety and tolerability of LPX-TI641 to placebo ( a look-alike solution) that contains no drug. We will also evaluate the plasma pharmacokinetics of LPX-TI641. LPX-TI6...

What is the current status of trial NCT06982352?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2025-06-15. Estimated completion is 2026-04-15.

What conditions does trial NCT06982352 study?

This clinical trial studies the following conditions: Atopic Dermatitis (AD), Psoriasis (PsO).

What interventions are being tested in trial NCT06982352?

The interventions under investigation include: Placebo (DRUG), LPX-TI641 (DRUG).

Who is sponsoring clinical trial NCT06982352?

This trial is sponsored by LAPIX Therapeutics, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06982352 being conducted?

This trial has 3 study locations across North Dakota, Texas, Jordan. 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

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