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NCT Number: NCT07819799

Safety, Tolerability and PK of ATTO 1091 in Healthy Adult Volunteers and Patients With Ulcerative Colitis

The goal of this clinical trial is to assess the safety, tolerability, and pharmacokinetics (PK) of ATTO-1091 in healthy adults and patients with ulcerative colitis.

The main questions it aims to answer are:

What medical problems do participants have when taking ATTO-1091? How long does ATTO-1091 stay in the body after dosing? Researchers will compare ATTO-1091 to a placebo (a look-alike substance that contains no drug).

Participants will be dosed with ATTO-1091 or a placebo, visit the clinic for checkups and tests, and keep a diary of their symptoms.

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Key information

About this study

This is a 3-part study. Parts 1 and 2 will be a single and multiple ascending dose design, respectively, assessing the safety, tolerability, and PK of ATTO-1091 in healthy adult volunteers. Part 3 will consist of multiple doses in adult participants with ulcerative colitis to assess safety, tolerability, and PK.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

  • Any sex or gender who is 18 to 60 years old, inclusive, at Screening.
  • Body weight of 45 to 125 kg, inclusive, 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.
  • Meets contraception requirements
  • Negative pregnancy test for participants of childbearing potential.

Part 3 (Participants with Ulcerative Colitis) Key Inclusion Criteria:

  • Any sex or gender who is 18 to 80 years old
  • Body weight of 45 to 125 kg and BMI between 17.0 and 40.0 kg/m2
  • UC diagnosis confirmed by endoscopy and histology ≥3 months prior to Screening
  • Moderately to severely active UC as defined by Modified Mayo Clinic Score (stool frequency, rectal bleeding, endoscopy) 5 to 9 inclusive, with Mayo endoscopic subscore ≥2 as confirmed by the central reader during Screening
  • Rectal bleeding subscore ≥1 and stool frequency subscore ≥1 at Screening.
  • Naïve to treatment with advanced therapies or has had an inadequate response, loss of response, or intolerance to no more than 3 drugs in 2 classes of the following:
  • Tumor necrosis factor (TNF-α) antagonists
  • Interleukin IL-12/IL-23 antagonists
  • Integrin inhibitors
  • JAK antagonists
  • S1P receptor agonists
  • Novel class with biologic-like activity (e.g. TL1A antagonists)
  • Meets washout criteria for prior UC therapies as specified in the protocol.
  • Negative pregnancy test for participants of childbearing potential

Parts 1&2 (Healthy Volunteers) Key Exclusion Criteria

  • Any clinically significant underlying illness
  • 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 uncontrolled asthma requiring systemic corticosteroids or hospitalization for asthma within 6 months prior to Day 1
  • History of hypersensitivity (including anaphylaxis) to a biologic medication, vaccine, immunoglobulin product (plasma-derived or recombinant, eg, monoclonal antibody), or to any of the IP excipients
  • 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 to approximately 40 mg nicotine) per day
  • History of drug or alcohol abuse
  • Laboratory values outside of the normal range considered clinically significant by the investigator

Part 3 (Participants with Ulcerative Colitis) Key Exclusion Criteria:

  • Any clinically significant underlying illness
  • 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 uncontrolled asthma requiring systemic corticosteroids or hospitalization for asthma within 6 months prior to Day 1
  • History of known primary immunodeficiency or is considered immunocompromised
  • Has been treated for a parasitic infection in the past 6 months
  • Participant has active HBV or HCV or is positive for HIV
  • Participant has active or latent TB
  • Stool positive for Clostridioides difficile toxin at Screening
  • Concomitant primary sclerosing cholangitis.
  • History of active major depressive episode or suicidal ideation
  • History of hypersensitivity (including anaphylaxis) to a biologic medication, vaccine, immunoglobulin product (plasma-derived or recombinant, eg, monoclonal antibody), or to any of the IP excipients
  • Diagnosis of non-UC or confounding GI conditions including Crohn's disease, indeterminate colitis, microscopic colitis, ischemic or radiation colitis.
  • Disease limited to isolated ulcerative proctitis (<15 cm).
  • Unresected colonic dysplasia or unresected adenomatous colonic polyps, fulminant colitis, toxic megacolon, bowel perforation, current colonic strictures, fistulae, stoma, ileostomy, colostomy, abdominal abscess, or anticipated need for colectomy during the study.
  • History of extensive colonic resection
  • History of drug or alcohol abuse
  • Laboratory values outside of the normal range considered clinically significant by the investigator

Treatment and study plan

ATTO-1091

Drug

ATTO-1091

Placebo

Drug

Placebo preparation to match ATTO-1091 dose

Primary outcomes

  1. Incidence of AEs

    Time frame: 0-169 Days for SAD; 0-204 Days for MAD in HV; 0-141 Days for MAD in UC

    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 28.0 or the current version). Their severity will be graded using the NCI CTCAE v5.0 or the current version.

  2. Incidence of laboratory abnormalities

    Time frame: 0-169 Days for SAD; 0-204 Days for MAD in HV; 0-141 Days for MAD in UC

    Clinical laboratory parameters (hematologic and blood chemistry) will be summarized by visit

  3. Incidence of ECG abnormalities

    Time frame: 0-169 Days for SAD; 0-204 Days for MAD in HV; 0-141 Days for MAD in UC

    ECG findings (including QT abnormalities) will be summarized by visit.

  4. Incidence of vital sign abnormalities

    Time frame: 0-169 Days for SAD; 0-204 Days for MAD in HV; 0-141 Days for MAD in UC

    Vital signs (systolic and diastolic blood pressure, temperature, heart rate) will be summarized by visit.

Secondary outcomes

  1. Incidence of Anti-drug Antibodies

    Time frame: 0-169 Days for SAD; 0-204 Days for MAD in HV; 0-141 Days for MAD in UC

    Baseline prevelance of ADA, changes in ADA status from prior to the first dose of IP to each applicable 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 ATT-1091.

  2. Peak Plasma Concentration (Cmax) of ATTO-1091

    Time frame: 0-169 Days for SAD; 0-204 Days for MAD in HV; 0-141 Days for MAD in UC

    The pharmacokinetics of single and multiple dose levels of ATTO-1091 in participants will include maximum concentration (Cmax) of ATTO-1091

  3. Circulating Half-life (t1/2) of ATTO-1091

    Time frame: 0-169 Days for SAD; 0-204 Days for MAD in HV; 0-141 for MAD in UC

    The pharmacokinetics of single and multiple dose levels of ATTO-1091 in participants will include half-life (t1/2) of ATTO-1091

  4. Area Under the Plasma Concentration versus Time Curve (AUC) ATTO-1091

    Time frame: 0-169 Days for SAD; 0-204 Days for MAD in HV; 0-141 for MAD in UC

    The pharmacokinetics of single and multiple dose levels of ATTO-1091 in participants will include area under the plasma concentration-time curve (AUC).

  5. Clearance Rate (C) for ATTO-1091

    Time frame: 0-169 Days for SAD; 0-204 Days for MAD in HV; 0-141 for MAD in UC

    The pharmacokinetics of single and multiple dose levels of ATTO-1091 in participants will include characterization of the clearance rate (C) of ATTO-1091.

  6. Volume of Distribution (V) of ATTO-1091

    Time frame: 0-169 Days for SAD; 0-204 Days for MAD in HV; 0-141 Days for MAD in UC

    The pharmacokinetics of single and multiple dose levels of ATTO-1091 in participants will include characterization of the Volume of distribution (V) of ATTO-1091.

Study contacts

Contact information is provided by the study sponsor or research team.

Malinda Longphre

CONTACT

[email protected]

15105203361

Sponsors and collaborators

Lead sponsor

Attovia Therapeutics Inc

Industry

Registry information

Official study title

A Phase 1, Multi-Part, Single Ascending Dose and Multiple Ascending Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of ATTO 1091 in Healthy Adult Volunteers and Patients With Ulcerative Colitis

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Sep 15, 2026
Registry last updated
Sep 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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