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CompletedNCT06787586Updated Sep 11, 2026

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

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

Phase
Phase 1
Study type
Interventional
Enrollment
108
Allocation
Randomized
Ages
18 Years to 85 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Normal Volunteers
  • Atopic Dermatitis (AD)
  • Atopic Eczema
  • Chronic Pruritus

Keywords

  • Atopic dermatitis
  • AD
  • Atopic eczema
  • Eczema
  • Chronic pruritis
  • Itch
  • Pruritus
03

In context

Dermatitis, Atopic

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Parts 1 \& 2 (Healthy Volunteers) Key Inclusion Criteria:

  • Any sex or gender who is 18 to 65 years old
  • Body weight of 50 to 125 kg and body mass index (BMI) between 18.5 and 35 kg/m2
  • Considered in good general health based on medical history, physical exam, 12-lead ECG, screening clinical laboratory findings, and vital signs
  • Negative pregnancy test for subjects of child-bearing potential
  • Use of highly effective forms of birth control

Part 3 (Subjects with Atopic Dermatitis) Inclusion Criteria:

  • Any sex or gender who is 18 to 65 years old
  • Body weight of 50 to 125 kg and BMI between 18.5 and 40 kg/m2
  • Clinically confirmed diagnosis of active AD
  • At least a 1-year history of AD and had no significant flares in AD for at least 4 weeks before Screening
  • Baseline weekly mean of daily PP-NRS ≥ 7 at Day 1
  • EASI score of ≥ 7 at Screening and Day 1
  • vIGA-AD score of ≥ 3 at Screening and Day 1
  • Use of topical bland emollient (moisturizer) once or twice daily for at least 5 of the 7 days immediately before Day 1 and agrees to continue using that same emollient at the same frequency throughout the study
  • Negative pregnancy test for subjects of child-bearing potential
  • Use of highly effective forms of birth control

Part 4 (Subjects with Chronic Pruritus) Inclusion Criteria:

  • Any sex or gender who is 18 to 85 years old
  • Body weight of 50 to 125 kg, inclusive, and BMI between 18.5 and 40 kg/m2
  • Has had chronic pruritus for at least 6 months and is unresponsive to at least a 2-week course of emollient use.
  • Chronic pruritus that affects at least 2 of the following body areas: legs, arms, or trunk
  • A single PP-NRS score of ≥ 5 in the 24-hour period prior to the Screening visit
  • Baseline weekly mean of daily PP-NRS ≥ 7 at Day 1
  • Use of a stable dose of topical bland emollient (moisturizer) once or twice daily for at least 2 weeks before Day 1 and agrees to continue using that same emollient at the same frequency throughout the study
  • Negative pregnancy test for subjects of child-bearing potential
  • Use of highly effective forms of birth control

Parts 1 \& 2 (Healthy Volunteers) Exclusion Criteria:

  • Any clinically significant underlying illness.
  • History of malignancy within 5 years of Screening, except adequately treated basal carcinoma or in situ carcinoma of the cervix.
  • History of major surgery within 8 weeks prior to Day 1
  • History of asthma requiring regular use of a bronchodilator or a daily maintenance therapy
  • History of hypersensitivity (including anaphylaxis) to a biologic medication, vaccine, an immunoglobulin product (plasma-derived or recombinant, eg, monoclonal antibody), or to any of the IP excipients (sucrose, polysorbate 80, or histidine)
  • Active hepatitis B virus (HBV) or hepatitis C virus (HCV) or is positive for HIV
  • Active or latent tuberculosis infection
  • Smoking more than 20 cigarettes (or cigars, cigarillos, or e-cigarettes equivalent) per day
  • History of drug or alcohol abuse
  • Laboratory values outside of the normal range

Exclusion Criteria for Part 3 (Subjects with Atopic Dermatitis):

  • Any clinically significant underlying illness
  • History of a clearly defined etiology for pruritus other than AD, including but not limited to urticaria, psoriasis, or other non-atopic dermatologic conditions, hepatic or renal disease, psychogenic pruritus, drug reaction, uncontrolled hyperthyroidism, and infection
  • History of malignancy within 5 years of Screening
  • History of major surgery within 8 weeks prior to Day 1 or has a major surgery planned during the study
  • History of asthma requiring regular use of a bronchodilator or a daily maintenance therapy
  • History of recurrent eczema herpeticum
  • History of known primary immunodeficiency, is considered immunocompromised, history of untreated latent tuberculosis infection, has been treated for active tuberculosis in the past year, or has been treated for a parasitic infection in the past 6 months
  • History of major depression
  • History of hypersensitivity (including anaphylaxis) to a biologic medication, vaccine, an immunoglobulin product (plasma-derived or recombinant, eg, monoclonal antibody), or to any of the IP excipients (sucrose, polysorbate 80, or histidine)
  • Active HBV or HCV or is positive for HIV
  • Smoking more than 20 cigarettes (or cigars, cigarillos, or e-cigarettes equivalent) per day
  • ECG with a QTcF > 450 msec for males or > 470 msec for females at Screening
  • History of drug or alcohol abuse
  • Subject has applied topical corticosteroid in the 14 days preceding Day 1
  • Subject has used prohibited medications or therapies during the specified washout period before Day 1 (as defined in the protocol)
  • Laboratory values outside of the normal range

Exclusion Criteria for Part 4 (Subjects with Chronic Pruritus):

  • Primary dermatologic diagnosis associated with pruritic skin lesions at the time of screening
  • Regional neuropathic disease associated with pruritus
  • Severe renal failure requiring dialysis
  • Untreated cholestatic liver disease
  • Liver function tests (bilirubin, AST, ALT, alkaline phosphatase) >2.5 times above the upper limit of normal
  • History of infectious dermatoses
  • Suspected diagnosis of somatoform pruritus
  • Suspected diagnosis of drug-induced pruritus
  • History of malignancy within 5 years of Screening
  • History of unexplained fevers, night sweats, or unintentional weight loss
  • Major surgery within 8 weeks prior to Day 1 or has a major surgery planned during the study
  • History of asthma requiring regular use of a bronchodilator or a daily maintenance therapy
  • History of known primary immunodeficiency, is considered immunocompromised, untreated latent tuberculosis infection, has been treated for active tuberculosis in the past year, or has been treated for a parasitic infection in the past 6 months
  • History of attempted suicide
  • History of hypersensitivity (including anaphylaxis) to a biologic medication, vaccine, an immunoglobulin product (plasma-derived or recombinant, eg, monoclonal antibody), or to any of the IP excipients (sucrose, polysorbate 80, or histidine)
  • Active HBV or HCV or is positive for HIV.
  • Smoking more than 20 cigarettes (or cigars, cigarillos, or e-cigarettes equivalent) per day
  • ECG with a QTcF > 450 msec for males or > 470 msec for females at Screening
  • History of drug or alcohol abuse
  • Use of prohibited medications as defined in the Protocol
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Sequential assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
108 participants (actual)

Study arms

  • Experimental
    ATTO-1310 single dose IV

    ATTO-1310 Attobody Dose level cohorts receiving a single dose IV

    Drug: ATTO-1310

  • Placebo comparator
    ATTO-1310 Placebo single dose IV

    Placebo preparation to match Experimental Arm with single dose IV

    Drug: ATTO-1310 Placebo

  • Experimental
    ATTO-1310 single dose SC

    ATTO-1310 Attobody Dose level cohorts receiving a single dose SC

    Drug: ATTO-1310

  • Placebo comparator
    ATTO-1310 Placebo single dose SC

    Placebo preparation to match Experimental Arm with single dose SC

    Drug: ATTO-1310 Placebo

  • Experimental
    ATTO-1310 multiple dose SC

    ATTO-1310 Attobody administered to dose level cohorts in multiple SC doses

    Drug: ATTO-1310

  • Placebo comparator
    ATTO-1310 Placebo multiple dose SC

    Placebo preparation to match Experimental Arm administered in multiple SC doses

    Drug: ATTO-1310 Placebo

Interventions

  • DrugATTO-1310

    ATTO-1310 Attobody

  • DrugATTO-1310 Placebo

    Placebo preparation to match ATTO-1310 Dose

06

What researchers measure

Primary outcomes

  1. 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

  2. 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

  3. 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

  4. 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

Secondary outcomes

  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

07

Study locations

17 sites
  • Attovia Clinical Site 103
    Encinitas, California 92024, United States
  • Attovia Clinical Site 116
    Rocklin, California 95765, United States
  • Attovia Clinical Site 107
    Sacramento, California 95815, United States
  • Attovia Clinical Site 109
    Coral Gables, Florida 33134, United States
  • Attovia Clinical Site 118
    Margate, Florida 33063, United States
  • Attovia Clinical Site 102
    Plainfield, Indiana 46168, United States
  • Attovia Clinical Site 104
    Saint Joseph, Missouri 64506, United States
  • Attovia Clinical Site 106
    Reno, Nevada 89509, United States
  • Attovia Clinical Site 114
    New York, New York 10029, United States
  • Attovia Clinical Site 119
    New York, New York 10128, United States
  • Attovia Clinical Site 108
    San Antonio, Texas 78213, United States
  • Attovia Clinical Site 110
    Fredericton, New Brunswick E3B1G9, Canada
  • Attovia Clinical Site 111
    Newmarket, Ontario L3Y 5G8, Canada
  • Attovia Clinical Site 112
    Peterborough, Ontario K9J 5K2, Canada
  • Attovia Clinical Site 113
    Toronto, Ontario M4W 2N4, Canada
  • Attovia Clinical Site 105
    Montreal, Quebec H2X2V1, Canada
  • Altasciences
    Montreal, Quebec H3P 3P1, Canada
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06787586
Lead sponsor
Attovia Therapeutics Inc
Responsible party
Sponsor
First posted
Jan 22, 2025
Start date
Jan 14, 2025
Primary completion
Jun 11, 2026
Completion
Jun 11, 2026
Last update
Sep 11, 2026

Study contacts

Eric Sicard, MD
principal investigator · Altasciences Company Inc.

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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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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