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Safety, Pharmacokinetics, and Pharmacodynamics of MTX-101 in Healthy Adults and Patients

Safety, Pharmacokinetics, and Pharmacodynamics of MTX-101 in Healthy Adults and Patients

Recruiting
18-65 years
All
Phase 1

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Overview

First in human study to understand the potential side effects of MTX-101, how long MTX-101 lasts in the human body, and how MTX-101 affects specific human immune cells.

Description

This is a prospective, multi-center, randomized, double-blind, placebo-controlled, single ascending dose (SAD) and multiple ascending dose (MAD) study to evaluate the safety, pharmacokinetics (PK), and pharmacodynamics (PD) of MTX-101 in healthy adults (HA) and participants with celiac disease (CeD) and type 1 diabetes (T1D). This study will enroll HAs only in Part A and CeD and T1D patients only in Part B.

Eligibility

Inclusion Criteria:

  • Adults, age ≥ 18 and ≤ 65 years at the time of anticipated dosing (Day 1).
  • Healthy individuals without known current or chronic medical conditions, including no history of any autoimmune diseases, in the opinion of the Investigator.
  • Body mass index (BMI) ≥ 18 kg/m2 and ≤ 32 kg/m2.
  • Body weight ≥ 45and ≤ 100 kg.
  • Negative Coronavirus Disease 2019 (COVID-19) test within 24 hours prior to each dose.
  • Persons of child-bearing potential must have a negative pregnancy test and either abstain from sex or use highly effective method(s) of birth control from Day 1 through the duration of the study.

Exclusion Criteria:

  • Clinically significant findings in physical examination (PE), vital signs (blood pressure, heart rate, and body temperature), electrocardiogram (ECG), and safety laboratory parameters at Screening in the opinion of the Investigator.
  • Renal function calculated by the Chronic Kidney Disease-Epidemiology (CKD-EPI) equation with estimated glomerular filtration rate (eGFR) < 90 mL/min/1.73 m2 or abnormal level of proteinuria detected by dipstick at the time of Screening.
  • Any disease or condition that, in the opinion of the Investigator, might significantly compromise the cardiovascular, hematological, renal, hepatic, pulmonary (including chronic asthma), endocrine (e.g., diabetes), central nervous, or gastrointestinal (including an ulcer) systems.
  • Receipt of an investigational drug within 28 days or 5 half-lives (whichever is longer) of the investigational drug(s) prior to Day 1.
  • Positive serology for human immunodeficiency virus (HIV) type 1 or 2, hepatitis (Hep) B surface antigen, or Hep C.
  • Positive test results for drug screen, including alcohol, at the time of Screening or on Day 1 prior to randomization.
  • Use of tobacco or nicotine-containing products more than the equivalent of 5 cigarettes/week within 30 days prior to (first) dosing.

Participants must abstain from nicotine use while inpatient.

  • History of receiving a live vaccine within 1 month of Screening.
  • History of splenectomy.
  • History of COVID or influenza vaccine within 2 weeks prior to Screening.
  • Planning to receive any vaccinations during the study period.
  • History of recurrent infections of uncertain cause.

Study details
    Healthy Volunteers
    Celiac Disease
    Type 1 Diabetes

NCT06324604

Mozart Therapeutics Australia Pty Ltd

6 September 2025

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