Relative Bioavailability and Effect of Food Study With AGMB-129 in Healthy Participants

NCT06397508 | Completed Phase 1

• 1 other identifier: AGMB-129-C103
• Study Type: interventional
• Target: 25
• Locations: 1 country
• Sites: 1

Brief Summary

This is a single-center, open-label, single-dose, randomized, 3-period cross-over, Phase 1 study in healthy adult participants to assess the BA of AGMB-129 tablet formulation relative to that of the reference capsule formulation and to assess the effect of food on the BA of a single oral dose of the AGMB-129 tablet formulation. A total of 24 participants will be enrolled. Participants will be randomized to 1 of 6 intervention sequences (Williams design) according to a 6-sequence, 3-period design. In 3 sequential intervention periods, each participant will receive 3 study interventions, 1 in each intervention period. The total duration of involvement for each participant, screening through follow-up, will be approximately 6 weeks.

Conditions

Healthy Volunteers

Outcome Measures

Primary Outcomes (9)

• Cmax for AGMB-129

  From baseline to Day 3

• Cmax for MET-158

  From baseline to Day 3

• Cmax for MET-154

  From baseline to Day 3

• AUC0-t for AGMB-129

  From baseline to Day 3

• AUC0-t for MET-158

  From baseline to Day 3

• AUC0-t for MET-154

  From baseline to Day 3

• AUC0-∞ for AGMB-447

  From baseline to Day 3

• AUC0-∞ for MET-158

  From baseline to Day 3

• AUC0-∞ for MET-154

  From baseline to Day 3

Secondary Outcomes (4)

• Number of participants with adverse events

  From Screening to Day 5

• Number of participants with abnormal clinical laboratory values

  From Screening to Day 5

• Number of participants with abnormal vital signs

  From Screening to Day 5

• Number of participants with abnormal physical exams

  From Screening to Day 5

Study Arms (6)

1

EXPERIMENTAL

ABC with A=oral capsule under fed conditions B=oral tablet under fasted conditions C=oral tablet under fed conditions

Drug: AGMB-129

2

EXPERIMENTAL

CAB with A=oral capsule under fed conditions B=oral tablet under fasted conditions C=oral tablet under fed conditions

Drug: AGMB-129

3

EXPERIMENTAL

BCA with A=oral capsule under fed conditions B=oral tablet under fasted conditions C=oral tablet under fed conditions

Drug: AGMB-129

4

EXPERIMENTAL

CBA with A=oral capsule under fed conditions B=oral tablet under fasted conditions C=oral tablet under fed conditions

Drug: AGMB-129

5

EXPERIMENTAL

BAC with A=oral capsule under fed conditions B=oral tablet under fasted conditions C=oral tablet under fed conditions

Drug: AGMB-129

6

EXPERIMENTAL

ACB with A=oral capsule under fed conditions B=oral tablet under fasted conditions C=oral tablet under fed conditions

Drug: AGMB-129

Interventions

AGMB-129 DRUG

Each participant will receive 3 study interventions, 1 in each intervention period

1; 2; 3; 4; 5; 6

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Male or female, between 18 and 55 years old (extremes included) on the date of signing the ICF.
• Body weight of at least 50.0 kg for men and 45.0 kg for women, and a body mass index (BMI) between 19.0 and 30.0 kg/m2 (extremes included) at screening.
• Must be in good health based on medical history, physical examination, vital signs, and 12-lead ECG in the opinion of the investigator at screening.
• Total bilirubin, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) must be ≤1.5x upper limit of normal (ULN) at screening. Other clinical laboratory safety test results must be within the reference ranges or test results that are outside the reference ranges need to be considered not clinically significant in the opinion of the investigator. Note: Participants with diagnosed Gilbert's syndrome with total bilirubin \>1.5 ULN are eligible for the study if AST and ALT are ≤1.5x ULN.

You may not qualify if:

• Known hypersensitivity to AGMB-129 ingredients or history of a significant allergic reaction to AGMB-129 ingredients as determined by the investigator.
• Positive serology for hepatitis B virus surface antigen (HBsAg) or anti-hepatitis C virus \[HCV\] antibodies at screening, or history of hepatitis from any cause except for hepatitis A that was resolved at least 3 months prior to the first IP administration.
• History of or a current immunosuppressive condition, including positive human immunodeficiency virus types 1 or 2 (HIV-1 \[2\]) antibodies at screening.
• Current or history of vasculitis, valvular heart disease, or large vessel vascular disease (such as aneurism or dissection) at screening.
• Any illness, judged by the investigator as clinically significant, in the 3 months prior to the first IP administration.
• Presence or sequelae of gastrointestinal, liver, kidney (estimated glomerular filtration rate \[eGFR\] ≤80 mL/min/1.73 m² using the Chronic Kidney Disease Epidemiology Collaboration \[CKD-EPI\] formula) or other conditions known to interfere with the absorption, distribution, metabolism, or excretion of drugs at screening.
• History of malignancy within the past 5 years prior to screening, except for excised and curatively treated non-metastatic basal cell carcinoma, squamous cell carcinoma of the skin, or carcinoma in situ of cervix which is considered cured with minimal risk of recurrence.
• History or presence of clinically significant abnormalities detected on 12-lead ECG of either rhythm or conduction, e.g., known long QT syndrome or a QT interval corrected for heart rate according to Fridericia's formula (QTcF) \>450 ms detected on the 12-lead ECG at screening or Day 1 predose. A first-degree atrioventricular block will not be considered as a clinically significant abnormality.

Sponsors & Collaborators

• Agomab Spain S.L.: lead

Study Sites (1)

SGS Belgium

Edegem, Belgium

Location

Study Officials

• Philippe Wiesel, MD

  Agomab Therapeutics

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: BASIC SCIENCE
• Intervention Model: SEQUENTIAL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 30, 2024
• First Posted: May 3, 2024
• Study Start: April 2, 2024
• Primary Completion: May 8, 2024
• Study Completion: May 13, 2024
• Last Updated: May 16, 2024

Record last verified: 2024-05

Data Sharing

• IPD Sharing: Will not share

Locations

BE (1)