ATTO-1091
DrugATTO-1091
NCT Number: NCT07819799
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.
Trial opening soon.
Get Notified18 year–65 year
All sexes
Interventional
Phase 1
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Parts 1&2 (Healthy Volunteers) Key Inclusion Criteria:
Part 3 (Participants with Ulcerative Colitis) Key Inclusion Criteria:
Parts 1&2 (Healthy Volunteers) Key Exclusion Criteria
Part 3 (Participants with Ulcerative Colitis) Key Exclusion Criteria:
ATTO-1091
Placebo preparation to match ATTO-1091 dose
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.
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
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.
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.
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.
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
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
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).
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.
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.
Contact information is provided by the study sponsor or research team.
Attovia Therapeutics Inc
Industry
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
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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