A Phase 1 interventional study of ATTO-1310 and ATTO-1310 Placebo in Normal Volunteers, Atopic Dermatitis (AD) and Atopic Eczema, sponsored by Attovia Therapeutics Inc. Completed at 17 sites in 2 countries. Open to participants aged 18 Years to 85 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-11.
Sponsored by Attovia Therapeutics Inc · Phase 1, Interventional, and Treatment
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.
This is a 4-part study. Parts 1 and 2 will be a single and multiple ascending dose design, respectively, assessing the safety, tolerability and PK of ATTO-1310 in healthy adult volunteers. Part 3 and Part 4 will consist of a single dose in adult patients with atopic dermatitis or chronic pruritus, respectively, to assess safety, tolerability, PK, and PD based on biomarkers in the blood.
1,419 studies on the registry are indexed under Dermatitis, Atopic; 258 are open to participants now.
This study's enrollment of 108 is above the median of 83 across 1,125 interventional studies indexed under Dermatitis, Atopic.
Browse Dermatitis, Atopic studies →Attovia Therapeutics Inc is the lead sponsor of 4 studies on the registry; 2 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Parts 1 \& 2 (Healthy Volunteers) Key Inclusion Criteria:
Part 3 (Subjects with Atopic Dermatitis) Inclusion Criteria:
Part 4 (Subjects with Chronic Pruritus) Inclusion Criteria:
Parts 1 \& 2 (Healthy Volunteers) Exclusion Criteria:
Exclusion Criteria for Part 3 (Subjects with Atopic Dermatitis):
Exclusion Criteria for Part 4 (Subjects with Chronic Pruritus):
ATTO-1310 Attobody Dose level cohorts receiving a single dose IV
Drug: ATTO-1310
Placebo preparation to match Experimental Arm with single dose IV
Drug: ATTO-1310 Placebo
ATTO-1310 Attobody Dose level cohorts receiving a single dose SC
Drug: ATTO-1310
Placebo preparation to match Experimental Arm with single dose SC
Drug: ATTO-1310 Placebo
ATTO-1310 Attobody administered to dose level cohorts in multiple SC doses
Drug: ATTO-1310
Placebo preparation to match Experimental Arm administered in multiple SC doses
Drug: ATTO-1310 Placebo
ATTO-1310 Attobody
Placebo preparation to match ATTO-1310 Dose
Incidence of AEs
The primary analysis will describe the incidence of AEs and laboratory abnormalities. AEs will be coded according to system organ class and preferred term using the Medical Dictionary for Regulatory Activities (MedDRA, version 26.1 or the current version). Their severity will be graded using the NCI CTCAE v5.0 or the current version.
Time frame: 0-113 Days for SAD; 0-143 Days for MAD
Incidence of laboratory abnormalities
Clinical laboratory parameters (hematologic and blood chemistry) will be summarized for each post-baseline visit.
Time frame: 0-113 Days for SAD; 0-143 Days for MAD
Incidence of ECG abnormalities
ECG findings (including QT abnormalities) will be summarized for each post-baseline visit.
Time frame: 0-113 Days for SAD; 0-143 Days for MAD
Incidence of vital sign abnormalities
Vital signs (systolic and diastolic blood pressure, temperature, heart rate) will be summarized for each post-baseline visit.
Time frame: 0-113 Days for SAD; 0-143 Days for MAD
Incidence of Anti-Drug Antibodies
Baseline prevalence of ADA, Changes in ADA status from prior to the first dose of IP to each post-dose timepoint and ADA titer values for samples confirmed positive for ADA will be evaluated to assess the immunogenicity of single and multiple dose levels of ATTO-1310.
Time frame: 0-113 Days for SAD; 0-143 Days for MAD
Peak plasma concentration (Cmax) ATTO-1310
The pharmacokinetics of single and multiple dose levels of ATTO-1310 in participants will include maximum concentration (Cmax)of ATTO-1310
Time frame: 0-113 Days for SAD; 0-143 Days for MAD
Circulating half-life of ATTO-1310 (t1/2)
The pharmacokinetics of single and multiple dose levels of ATTO-1310 in participants will include half-life (t1/2) of ATTO-1310
Time frame: 0-113 Days for SAD; 0-143 Days for MAD
Area Under the Plasma Concentration Versus Time Curve (AUC)
The pharmacokinetics of single and multiple dose levels of ATTO-1310 in participants will include area under the plasma concentration-time curve (AUC).
Time frame: 0-113 Days for SAD; 0-143 Days for MAD
Clearance rate (C) of ATTO-1310
The pharmacokinetics of single and multiple dose levels of ATTO-1310 in participants will include characterization of the Clearance rate (C) of ATTO-1310
Time frame: 0-113 Days for SAD; 0-143 Days for MAD
Volume of Distribution (V) of ATTO-1310
The pharmacokinetics of single and multiple dose levels of ATTO-1310 in participants will include characterization of the Volume of distribution (V) of ATTO-1310
Time frame: 0-113 Days for SAD; 0-143 Days for MAD
Bioavailability (F) of ATTO-1310
The pharmacokinetics of single and multiple dose levels of ATTO-1310 in participants will include characterization of the Bioavailability (F) of ATTO-1310
Time frame: 0-113 Days for SAD; 0-143 Days for MAD
Plan to share: No
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This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.
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Attovia Therapeutics Inc