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Not yet recruitingNCT07819799Updated Sep 15, 2026

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

A Phase 1 interventional study of ATTO-1091 and Placebo in Ulcerative Colitis (UC), sponsored by Attovia Therapeutics Inc. Not yet recruiting. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-15.

Sponsored by Attovia Therapeutics Inc · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
96
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study 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 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.

02

Conditions studied

  • Ulcerative Colitis (UC)

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Keywords

  • ulcertive colitis
  • IBD
  • UC
03

In context

Colitis, Ulcerative

1,853 studies on the registry are indexed under Colitis, Ulcerative; 472 are open to participants now.

This study's planned enrollment of 96 is above the median of 70 across 1,236 interventional studies indexed under Colitis, Ulcerative.

Browse Colitis, Ulcerative 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 65 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 60 years old, inclusive, at Screening.
  • Body weight of 45 to 125 kg, inclusive, and (BMI) between 18.5 and 35 kg/m2.
  • Considered in good general health based on medical history, physical exam, 12-lead , screening clinical laboratory findings, and vital signs.
  • Meets requirements
  • Negative pregnancy test for participants of .

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 underlying illness
  • History of 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 or hospitalization for asthma within 6 months prior to Day 1
  • History of (including anaphylaxis) to a biologic medication, vaccine, immunoglobulin product (plasma-derived or recombinant, eg, monoclonal antibody), or to any of the IP
  • Active virus (HBV) or virus (HCV) or is positive for
  • 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
  • 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
Terms in these criteria, in plain language(13)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

Excipients

The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

05

Study design

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

Study arms

  • Experimental
    ATTO-1091 Single dose SC

    ATTO-1091 Dose level cohorts receiving a single dose SC

    Drug: ATTO-1091

  • Experimental
    ATTO-1091 Multiple dose SC

    ATTO-1091 Dose level cohorts receiving multiple SC doses

    Drug: ATTO-1091

  • Experimental
    Placebo single dose SC

    Placebo preparation to match Experimental Arm with single dose SC

    Drug: Placebo

  • Experimental
    Placebo multiple dose SC

    Placebo preparation to match Experimental Arm administered in multiple SC doses

    Drug: Placebo

Interventions

  • DrugATTO-1091

    ATTO-1091

  • DrugPlacebo

    Placebo preparation to match ATTO-1091 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 28.0 or the current version). Their severity will be graded using the NCI CTCAE v5.0 or the current version.

    Time frame: 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

    Time frame: 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.

    Time frame: 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.

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

Secondary outcomes

  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.

    Time frame: 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

    Time frame: 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

    Time frame: 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).

    Time frame: 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.

    Time frame: 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.

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

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Dec 2026; primary completion for Jul 2028, 19 months later.

Of 57 industry-sponsored phase 1 interventional studies under Colitis, Ulcerative, half reached primary completion within 12 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 17. This study's planned 19 months is above that.

Counting every sponsor, half of 83 studies reached it within 13 months; a quarter within 8 and three quarters within 26.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 9, 2026
First posted
Sep 15, 2026
StartEst.
Dec 14, 2026
Primary completionEst.
Jul 15, 2028
CompletionEst.
Jul 15, 2028
Last update
Sep 15, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07819799
Lead sponsor
Attovia Therapeutics Inc
Responsible party
Sponsor
First posted
Sep 15, 2026
Start date
Dec 14, 2026 (estimated)
Primary completion
Jul 15, 2028 (estimated)
Completion
Jul 15, 2028 (estimated)
Last update
Sep 15, 2026

Study contacts

Malinda Longphre
Contact
mlongphre@attovia.com
15105203361
Hubert Chen, MD
study director · Attovia Therapeutics Inc

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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