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Ulcerative Colitis (UC)Phase 1NCT07819799

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

A Phase 1 study testing ATTO-1091 in people with Ulcerative Colitis (UC), run by Attovia Therapeutics Inc.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Ulcerative Colitis (UC)
What is being tested?
ATTO-1091
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
96 participants
Where
No sites listed yet
Study dates
14 Dec 2026to 15 Jul 2028
Phase
Phase 1
Are there results?
Not yet: the study is under way

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 65 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 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

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Malinda Longphre contact

15105203361

mlongphre@attovia.com

About this study

Official 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

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.

Read the detailed description

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.

Being tested
ATTO-1091, Placebo
Keywords
ulcertive colitis, IBD, UC
Medical subject headings
Colitis, Ulcerative

What participants receive

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

  • ATTO-1091Drug

    ATTO-1091

  • PlaceboDrug

    Placebo preparation to match ATTO-1091 dose

Study groups in NCT07819799
Study groupRoleWhat they receive
ATTO-1091 Single dose SCExperimentalATTO-1091 Dose level cohorts receiving a single dose SC
Receives: Drug: ATTO-1091
ATTO-1091 Multiple dose SCExperimentalATTO-1091 Dose level cohorts receiving multiple SC doses
Receives: Drug: ATTO-1091
Placebo single dose SCExperimentalPlacebo preparation to match Experimental Arm with single dose SC
Receives: Drug: Placebo
Placebo multiple dose SCExperimentalPlacebo preparation to match Experimental Arm administered in multiple SC doses
Receives: Drug: 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 28.0 or the current version). Their severity will be graded using the NCI CTCAE v5.0 or the current version.

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

  2. Incidence of laboratory abnormalities

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

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

  3. Incidence of ECG abnormalities

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

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

  4. Incidence of vital sign abnormalities

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

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

Secondary outcomes (6)
  1. Incidence of Anti-drug Antibodies

    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.

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

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

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

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

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

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

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

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

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

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

  5. Clearance Rate (C) for ATTO-1091

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

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

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

    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.

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

Timeline

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

  1. First posted15 Sep 2026
  2. Study start14 Dec 2026 (estimated)
  3. Primary completion15 Jul 2028 (estimated)
  4. Study completion15 Jul 2028 (estimated)

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
96 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07819799
Sponsor's protocol ID
ATTO-1091-101
Status last verified
Sep 2026
First submitted
9 Sep 2026
Last updated
15 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing ATTO-1091 in people with Ulcerative Colitis (UC), run by Attovia Therapeutics Inc.

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: opening soon, as of the sponsor's last update on 15 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Malinda Longphre (15105203361, mlongphre@attovia.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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 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 15 Sep 2026.

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