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.
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.
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.
- Conditions
- Ulcerative Colitis (UC)
- 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 group | Role | What they receive |
|---|---|---|
| ATTO-1091 Single dose SC | Experimental | ATTO-1091 Dose level cohorts receiving a single dose SC Receives: Drug: ATTO-1091 |
| ATTO-1091 Multiple dose SC | Experimental | ATTO-1091 Dose level cohorts receiving multiple SC doses Receives: Drug: ATTO-1091 |
| Placebo single dose SC | Experimental | Placebo preparation to match Experimental Arm with single dose SC Receives: Drug: Placebo |
| Placebo multiple dose SC | Experimental | Placebo 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.
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
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
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
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)
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
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
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
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
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
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.
- First posted15 Sep 2026
- Study start14 Dec 2026 (estimated)
- Primary completion15 Jul 2028 (estimated)
- Study completion15 Jul 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Ulcerative Colitis (UC)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Attovia Therapeutics Inc
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Hubert Chen, MD, Study director, Attovia Therapeutics Inc
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
Study at a glance
From the registry record, last updated by the sponsor on 15 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT07819799
- Acronym / sponsor ID
- ATTO-1091-101
- Conditions
- Ulcerative Colitis (UC)
- Keywords
- ulcertive colitis, IBD, UC
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 96 participants (estimated)
- Lead sponsor
- Attovia Therapeutics IncIndustry (pharma, biotech, devices)
- Study start
- 14 Dec 2026 (estimated)
- Primary completion
- 15 Jul 2028 (estimated)
- Study completion
- 15 Jul 2028 (estimated)
- First posted
- 15 Sep 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 4
- Model description
- Single ascending dose, multiple ascending dose, randomized, double-blind, placebo-controlled
| Arm | Type | Receives |
|---|---|---|
| ATTO-1091 Single dose SC | Experimental | Drug: ATTO-1091ATTO-1091 Dose level cohorts receiving a single dose SC |
| ATTO-1091 Multiple dose SC | Experimental | Drug: ATTO-1091ATTO-1091 Dose level cohorts receiving multiple SC doses |
| Placebo single dose SC | Experimental | Drug: PlaceboPlacebo preparation to match Experimental Arm with single dose SC |
| Placebo multiple dose SC | Experimental | Drug: PlaceboPlacebo preparation to match Experimental Arm administered in multiple SC doses |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ATTO-1091ATTO-1091 | Drug | ATTO-1091 Multiple dose SC, ATTO-1091 Single dose SC |
| PlaceboPlacebo preparation to match ATTO-1091 dose | Drug | Placebo multiple dose SC, Placebo single dose SC |
Primary outcome
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.
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
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.
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.
6 secondary outcomes
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
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
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
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
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
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
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Sep 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Hubert Chen, MD study director
Attovia Therapeutics Inc
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.