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Active, Not Recruiting

NCT Number: NCT07505303

MIST (Metabolic Intervention With Semaglutide and THR-β Therapy) Trial

The primary objective of this trial is to evaluate the effect of oral ECC4703 on body weight reduction and in a sub-study on liver fat content as assessed by change in magnetic resonance imaging proton density fat fraction (MRI-PDFF) at Week 20.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Central Research Associates - Flourish - PPDS, Birmingham, Alabama, United States

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Capable of providing written informed consent and complying with all trial procedures.
  • Willing to comply with contraception requirements (as applicable to males and females of childbearing potential).
  • Obese with BMI ≥30 kg/m^2 and stable body weight within 6 months prior to screening.
  • HbA1c ≤6.5%.
  • Estimated glomerular filtration rate (eGFR) ≥60 mL/min/1.73 m^2 (per CKD-EPI 2021 formula).
  • If participant consents to enter the imaging substudy, has liver fat content by MRI-PDFF >8% at baseline (Week 9).

Exclusion criteria

  • History or current diagnosis of type 1 or type 2 diabetes mellitus.
  • Weight change >5% of total body weight within 6 months prior to screening or planned initiation of a weight loss program or use of weight-altering medication.
  • Obesity induced by endocrine disorders such as Cushing's syndrome or monogenic or syndromic obesity such as Prader-Willi syndrome.
  • Use of GLP-1 agonist treatment within the last 6 months prior to screening.
  • History or current evidence of a pituitary disorder.
  • Have current treatment with or history (within 3 months prior to screening) of treatment with medications that may cause significant weight gain.
  • ALT or AST >1.5×ULN, or ALP >1.5×ULN at screening.
  • Documented evidence or clinical signs/symptoms of advanced liver disease including liver cirrhosis, portal hypertension, or hepatic decompensation.
  • History of significant alcohol consumption for >3 consecutive months within a year prior to screening.
  • Current or past therapy with THR-β agonists (eg, resmetirom).
  • Active untreated hyperthyroidism or hyperthyroidism currently treated with antithyroid medications including methimazole or propylthiouracil.
  • Clinically significant thyroid dysfunction including uncontrolled hypothyroidism or hyperthyroidism.
  • History of bariatric surgery, fitting of a weight loss device, or intestinal bypass surgery within 5 years prior to screening.
  • History of major surgery within 8 weeks prior to screening.
  • Clinically relevant acute or chronic medical condition or unstable disease of the cardiovascular, gastrointestinal, hepatic, renal, endocrine, pulmonary, neurologic, psychiatric, immune or dermatologic system.

Treatment and study plan

ECC4703

Drug

orally QD

Placebo

Drug

orally QD

semaglutide

Drug

SC once weekly

Primary outcomes

  1. Percentage Change in Body Weight from Baseline (Week 9) to Week 20

    Time frame: Baseline (Week 9) to Week 20

  2. Proportion of Participants Achieving ≥5% Reduction in Body Weight from Baseline (Week 9) to Week 20

    Time frame: Baseline (Week 9) to Week 20

  3. Absolute Change in Liver Fat Content as Measured by MRI-PDFF in Participants With Hepatic Steatosis

    Time frame: Baseline (Week 9) to Week 20

  4. Percentage Change in Liver Fat Content as Measured by MRI-PDFF in Participants With Hepatic Steatosis

    Time frame: Baseline (Week 9) to Week 20

  5. Proportion of Participants With ≥30% Relative Reduction in Liver Fat Content as Measured by MRI-PDFF

    Time frame: Baseline (Week 9) to Week 20

Secondary outcomes

  1. Change in Percentage Lean Mass as Measured by DXA

    Time frame: Baseline (Week 9) to Week 20

  2. Change in Percentage Total Body Fat Mass as Measured by DXA

    Time frame: Baseline (Week 9) to Week 20

  3. Change in Percentage Visceral Fat Mass as Measured by DXA

    Time frame: Baseline (Week 9) to Week 20

  4. Change in Glycemic Parameters from Baseline (Week 9) to Week 20

    Time frame: Baseline (Week 9) to Week 20

    Change in HbA1c and fasting plasma glucose levels from baseline (Week 9) to Week 20

  5. Change in Lipid Parameters from Baseline (Week 9) to Week 20

    Time frame: Baseline (Week 9) to Week 20

  6. Change in Body Weight (kg) from Baseline (Week 9) to Week 20

    Time frame: Baseline (Week 9) to Week 20

  7. Proportion of Participants Achieving ≥2% and ≥3% Reduction in Body Weight from Baseline (Week 9) to Week 20

    Time frame: Baseline (Week 9) to Week 20

  8. Change in Alanine Aminotransferase (ALT) Levels from Baseline (Week 9) to Week 20

    Time frame: Baseline (Week 9) to Week 20

  9. Change in Aspartate Aminotransferase (AST) Levels from Baseline (Week 9) to Week 20

    Time frame: Baseline (Week 9) to Week 20

  10. Change in Alkaline Phosphatase (ALP) Levels from Baseline (Week 9) to Week 20

    Time frame: Baseline (Week 9) to Week 20

  11. Change in Gamma-Glutamyl Transferase (GGT) Levels from Baseline (Week 9) to Week 20

    Time frame: Baseline (Week 9) to Week 20

  12. Frequency of Treatment-Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)

    Time frame: From first dose through Week 20 (or end of study visit)

  13. Severity of Treatment-Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)

    Time frame: From first dose through Week 20 (or end of study visit)

  14. Laboratory Safety Evaluations

    Time frame: Baseline through Week 20

    changes in clinical laboratory parameters, including hematology, serum chemistry, and urinalysis.

  15. Changes in 12-Lead Electrocardiogram (ECG) Parameters

    Time frame: Baseline through Week 20

    Change in QT Interval, etc

  16. Changes in Vital Signs Findings

    Time frame: Baseline through Week 20

    including blood pressure, etc

  17. Changes in Physical Examination Findings

    Time frame: Baseline through Week 20

    including blood pressure, etc

Sponsors and collaborators

Lead sponsor

Eccogene

Industry

Registry information

Official study title

A Phase 2a, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Efficacy, Safety, and Tolerability of ECC4703 as an Adjunct to Semaglutide in Adults With Obesity

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 1, 2026
Registry last updated
Jun 25, 2026

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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