Phase I Study to Assess Safety, Tolerability, PK and PD of AGMB-447 in Healthy Participants and Participants With IPF

Prior treatment

• After a minimum of 10 minutes supine rest at the time of screening or prior to randomization on Day -1 or Day 1 of treatment period 1:
  • Systolic blood pressure \<90 or \>150 mmHg, or
  • Diastolic blood pressure \<50 or \>95 mmHg, or
  • Pulse \<40 or \>90 bpm
• Any clinically significant abnormalities in resting ECG at the time of screening or prior to randomization on Day -1 or Day 1 of treatment period 1 including prolonged QTcF (\>450 ms for males; \>470 ms for females using the mean of triplicate ECG's) and cardiac arrhythmias, as judged by the Investigator.
• Any clinically significant abnormalities in resting ECG at the time of screening or prior to randomization on Day -1 or Day 1 including prolonged QTcF (\>450 ms for males; \>470 ms for females using the mean of triplicate ECG's) and cardiac arrhythmias, as judged by the Investigator.
• Acute IPF exacerbation within 3 months prior to screening and/or during the screening period prior to dose on Day 1 as determined by the Investigator.
• Any signs of respiratory tract infection within 4 weeks of screening or prior to dosing on Day 1 that is deemed clinically significant in the opinion of the Investigator.

Other illness

• History or presence of any clinically relevant acute or chronic medical or psychiatric condition that could interfere with the participant's safety during the clinical study or expose the participant to undue risk as judged by the Investigator.
• History or presence of any clinically relevant acute or chronic medical or psychiatric condition that could interfere with the participant's safety during the clinical study or expose the participant to undue risk as judged by the Investigator.
• Malignancy within the past 5 years of screening with the exception of in situ removal of basal cell carcinoma or resected benign colonic polyps.

Lab values

• Clinically significant abnormalities in renal function at screening including any of the following:
  • Serum creatinine \>2 x ULN
  • eGFR \<80 mL/min
• Clinically significant abnormalities in liver function at screening including any of the following:
  • Bilirubin \>1.5 x ULN
  • Aminotransferases \>2 x ULN
  • ALP \>1.5 x ULN
• Clinically significant abnormalities in liver function at screening including any of the following:
  • Bilirubin \>1.5 x ULN
  • Aminotransferases \>2 x ULN
  • ALP \>1.5 x ULN

Other

• History or presence of any clinically significant pulmonary abnormalities, with the exception of IPF, in the opinion of the Investigator.
• Relevant airways obstruction (pre-bronchodilator FEV1/ FVC \< 0.7) at screening.

• Male and female participants aged between 18-55 years inclusive, at the time of informed consent.
• Participants must have FEV1 ≥80% predicted at screening and prior to randomization on Day -1 or Day 1 of treatment period 1 (using Global Lung Index, GLI 2012, predicted values).
• Participant must have a body weight of at least 50.0 kg and BMI ≥ 18 and ≤ 32 kg/m2 at screening.
• Participants must be in good health as determined by medical history, physical examination, vital signs, 12-lead ECG, spirometry and clinical laboratory assessments at the time of screening, as judged by the Investigator.
• Male and female participants aged \>40 years inclusive, at the time of informed consent.
• Participants must have a confirmed diagnosis of IPF (IPF based on 2022 ATS/ERS/JRS/ALAT Guidelines) as confirmed by the Investigator based on chest High Resolution Computed Tomography Scan taken within 5 years of screening and, only if available, surgical lung biopsy)
• Participants must be either:
• Receiving a stable, well tolerated dose of Nintedanib for 3 months prior to screening for the treatment of IPF
• OR
• Receiving no current antifibrotic medication for the treatment of IPF. This includes those who have never received treatment and those who have stopped medication due to intolerance for any reason, except non-responsiveness, for at least 6 weeks prior to screening.
• Participants must have FVC ≥40% of predicted (using Global Lung Index, GLI 2012, predicted values) at screening.
• Participants must have DLCO (corrected for hemoglobin ) ≥ 25% of predicted (using Global Lung Index, GLI 2017, predicted values) at screening.
• Participants must have FEV1 ≥30% predicted at screening and prior to randomization on Day -1 or Day 1 (using Global Lung Index, GLI 2012, predicted values).