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Normal VolunteersPhase 1NCT06787586

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

A Phase 1 study testing ATTO-1310 in people with Normal Volunteers and Atopic Dermatitis (AD), run by Attovia Therapeutics Inc at 17 sites in 2 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 85 yearsHealthy volunteers can take part
What is being tested?
ATTO-1310
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
108 participants
Where
17 sitesin 2 countries
Study dates
14 Jan 2025to 11 Jun 2026
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 85 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

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

Trial locations and contacts

17 sites in 2 countries.

17 sites in 2 countries

United States11 sites
  • Attovia Clinical Site 109

    Coral Gables, Florida, 33134

  • Attovia Clinical Site 103

    Encinitas, California, 92024

  • Attovia Clinical Site 118

    Margate, Florida, 33063

  • Attovia Clinical Site 114

    New York, New York, 10029

  • Attovia Clinical Site 119

    New York, New York, 10128

  • Attovia Clinical Site 102

    Plainfield, Indiana, 46168

  • Attovia Clinical Site 106

    Reno, Nevada, 89509

  • Attovia Clinical Site 116

    Rocklin, California, 95765

  • Attovia Clinical Site 107

    Sacramento, California, 95815

  • Attovia Clinical Site 104

    Saint Joseph, Missouri, 64506

  • Attovia Clinical Site 108

    San Antonio, Texas, 78213

Other trials in United States

Canada6 sites
  • Attovia Clinical Site 110

    Fredericton, New Brunswick, E3B1G9

  • Attovia Clinical Site 105

    Montreal, Quebec, H2X2V1

  • Altasciences

    Montreal, Quebec, H3P 3P1

  • Attovia Clinical Site 111

    Newmarket, Ontario, L3Y 5G8

  • Attovia Clinical Site 112

    Peterborough, Ontario, K9J 5K2

  • Attovia Clinical Site 113

    Toronto, Ontario, M4W 2N4

Other trials in Canada

About this study

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

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.

Being tested
ATTO-1310, ATTO-1310 Placebo
Keywords
Atopic dermatitis, AD, Atopic eczema, Eczema, Chronic pruritis, Itch, Pruritus
Medical subject headings
Dermatitis, Atopic, Eczema, Pruritus

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ATTO-1310Drug

    ATTO-1310 Attobody

  • ATTO-1310 PlaceboDrug

    Placebo preparation to match ATTO-1310 Dose

Study groups in NCT06787586
Study groupRoleWhat they receive
ATTO-1310 single dose IVExperimentalATTO-1310 Attobody Dose level cohorts receiving a single dose IV
Receives: Drug: ATTO-1310
ATTO-1310 Placebo single dose IVPlacebo comparatorPlacebo preparation to match Experimental Arm with single dose IV
Receives: Drug: ATTO-1310 Placebo
ATTO-1310 single dose SCExperimentalATTO-1310 Attobody Dose level cohorts receiving a single dose SC
Receives: Drug: ATTO-1310
ATTO-1310 Placebo single dose SCPlacebo comparatorPlacebo preparation to match Experimental Arm with single dose SC
Receives: Drug: ATTO-1310 Placebo
ATTO-1310 multiple dose SCExperimentalATTO-1310 Attobody administered to dose level cohorts in multiple SC doses
Receives: Drug: ATTO-1310
ATTO-1310 Placebo multiple dose SCPlacebo comparatorPlacebo preparation to match Experimental Arm administered in multiple SC doses
Receives: Drug: ATTO-1310 Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: 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.

    Measured: 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.

    Measured: 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.

    Measured: 0-113 Days for SAD; 0-143 Days for MAD

Secondary outcomes (7)
  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.

    Measured: 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

    Measured: 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

    Measured: 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).

    Measured: 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

    Measured: 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

    Measured: 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

    Measured: 0-113 Days for SAD; 0-143 Days for MAD

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jan 2025
  2. Study start14 Jan 2025
  3. Primary completion11 Jun 2026
  4. Study completion11 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Sequential
Model description
Single ascending dose, multiple ascending dose, randomized, double-blind, placebo-controlled
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
108 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06787586
Sponsor's protocol ID
ATTO-1310-101
Status last verified
Sep 2026
First submitted
26 Dec 2024
Last updated
11 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing ATTO-1310 in people with Normal Volunteers and Atopic Dermatitis (AD), run by Attovia Therapeutics Inc at 17 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 17 sites in United States, Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Incidence of AEs (time frame: 0-113 Days for SAD; 0-143 Days for MAD). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Sep 2026.

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