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Completed Phase 1 Interventional Accepts healthy volunteers

Safety, Tolerability and PK of ATTO-1310 in Healthy Volunteers and Patients With Atopic Dermatitis and Patients With Chronic Pruritus

ClinicalTrials.gov ID: NCT06787586

Public ClinicalTrials.gov record NCT06787586. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 4:12 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Multi-Part, Single Ascending Dose and Multiple Ascending Dose Study to Assess the Safety, Tolerability, and PK of ATTO1310 in Adult Volunteers, Patients With Atopic Dermatitis, and Patients With Chronic Pruritus

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this clinical trial is to assess the safety, tolerability, and pharmacokinetics of ATTO-1310 in healthy adults, patients with atopic dermatitis and patients with chronic pruritus. The main questions it aims to answer are: What medical problems do participants have when taking ATTO-1310? How long does ATTO-1310 stay in the body after dosing? Researchers will compare ATTO-1310 to a placebo (a look-alike substance that contains no drug). Participants will be dosed with ATTO-1310 or a placebo, visit the clinic for checkups and tests, and keep a diary of their symptoms.

Study identification

NCT ID
NCT06787586
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Attovia Therapeutics Inc
Industry
Enrollment
108 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 85 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 14, 2025 (Actual)
Primary completion
Jun 11, 2026 (Actual)
Completion
Jun 11, 2026 (Actual)
Last update posted
Sep 11, 2026

2025 – 2026

United States locations

U.S. sites
11
U.S. states
7
U.S. cities
10
Facility City State ZIP Site status
Attovia Clinical Site 103 Encinitas California 92024 —
Attovia Clinical Site 116 Rocklin California 95765 —
Attovia Clinical Site 107 Sacramento California 95815 —
Attovia Clinical Site 109 Coral Gables Florida 33134 —
Attovia Clinical Site 118 Margate Florida 33063 —
Attovia Clinical Site 102 Plainfield Indiana 46168 —
Attovia Clinical Site 104 Saint Joseph Missouri 64506 —
Attovia Clinical Site 106 Reno Nevada 89509 —
Attovia Clinical Site 114 New York New York 10029 —
Attovia Clinical Site 119 New York New York 10128 —
Attovia Clinical Site 108 San Antonio Texas 78213 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06787586, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 11, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06787586 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →