A Phase 1 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Immunogenicity of HuL001

A Phase 1 Single and Multiple Dose Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Immunogenicity of HuL001 in Healthy Volunteers and Idiopathic Pulmonary Fibrosis Subjects

This is a first-in-human, two-part, Phase 1 study that will characterize the safety, tolerability, PK, and immunogenicity of HuL001.

Study Overview

• Status: Recruiting
• Conditions: Idiopathic Pulmonary Fibrosis
• Intervention / Treatment: Drug: HuL001

Detailed Description

This is a first-in-human, two-part, Phase 1 study that will characterize the safety, tolerability, PK, and immunogenicity of HuL001 after single ascending doses in healthy subjects followed by multiple doses in IPF subjects. The study will be conducted in 2 parts:

• Part A will enroll 3 single ascending doses (SAD) cohorts in healthy subjects. (HuL001:Placebo=4:2)
• Part B will enroll 1 multiple-dose cohort in IPF subjects. The proposed dose of HuL001 will be selected from the single-dose range of HuL001 evaluated in the healthy subjects of Part A. (HuL001=6)

• Study Type: Interventional
• Enrollment (Anticipated): 24
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: Zoe Chan, MS; Phone Number: 886226579668; Email: zoechan@hunilife.com

Study Locations

• Taiwan
  • New Taipei City, Taiwan
    • Completed
    • Mackay Memorial Hospital
  • Taipei, Taiwan
    • Recruiting
    • National Taiwan University Hospital
    • Contact: Daniel Chen; Phone Number: 886-8979-1033

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 55 years (Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

Subjects who meet the following criteria will be eligible to participate in the study:

Healthy and IPF Subjects

1. Female subjects and male subjects with female partners of child-bearing potential must agree to use adequate contraception (2 forms of birth control, one of which must be a barrier method). This criterion must be followed from the time of the first dose of treatment.
2. Able to understand, sign the written informed consent form, and follow the study procedures.
3. With no clinically significant abnormalities in vital signs, 12-lead ECG, and clinical laboratory assessments at screening as judged by the Investigator
4. Corrected QT interval using Fridericia's (QTcF) < 450 milliseconds (msec).

Healthy Subjects only

1. Aged between 20 and 55 years of age inclusive, at the time of signing the informed consent.
2. Alanine aminotransferase (ALT), alkaline phosphatase (ALP), and bilirubin ≤ 1.5x upper limit of normal (ULN) (isolated bilirubin > 1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin < 35%).
3. Body weight ≥ 50 kilogram (kg), < 75 kg and body mass index (BMI) within the range 19.0 - 29.9 kg/m2 (inclusive).

IPF Subjects only

1. Aged between 40 and 90 years of age inclusive, at the time of signing the informed consent.
2. FVC≥ 40% and DLCO≥30%
3. Alanine aminotransferase (ALT), alkaline phosphatase (ALP), and bilirubin ≤ 2x upper limit of normal (ULN) (isolated bilirubin > 2xULN is acceptable if bilirubin is fractionated and direct bilirubin < 35%).
4. Diagnosis of IPF as defined by ATS/ERS/JRS/ALAT guidelines (Raghu 2018) within the past 7 years prior to study participation.
5. Patients who are ineffective with an approved therapy (i.e., pirfenidone or nintedanib), or who are judged by the Investigator to be unsuitable for receiving approved therapy

Exclusion Criteria:

Subjects presenting with any of the following criteria will be excluded from participating in the study:

Healthy and IPF Subjects

1. Female subjects who are breastfeeding, pregnant, or planning to become pregnant during the study period.
2. The Investigator considers that the subject is not in the condition to participate in this study.
3. Evidence or history of clinically significant (as judged by the Investigator) hematologic, renal, endocrine, pulmonary (except for IPF subjects), gastrointestinal, cardiovascular (except for IPF subjects), hepatic, psychiatric, immunologic, metabolic, urologic, dermatologic, neurologic or allergic diseases, or other significant clinical findings within 3 months prior to screening.
4. Has participated in a clinical trial and has received an investigational product (IP) within 60 days prior to screening.
5. Previous history of anaphylaxis and severe allergic reaction, generation of neutralizing antibodies, or hypersensitivity to albumin or a protein-based therapeutic, or any other monoclonal antibody.
6. Had blood donation within 60 days or had blood donation over 250 mL within 90 days prior to screening, or cannot commit to stopping blood donation during the study period.
7. Receipt of vaccination within 1 month of screening or plan to receive vaccination during the study.
8. Have significant active infection (acute or chronic) within 28 days prior to screening.

Healthy Subjects only

1. A positive test for Human Immunodeficiency Virus (HIV) antibody, Hepatitis B surface antigen, or Hepatitis C antibody result within 3 months of screening.

2. Abnormal baseline blood tests exceeding any of the limits defined below:

   • ALT or aspartate transaminase (AST) > 1.5x ULN, ALP and bilirubin > 1.5x ULN (isolated bilirubin > 1.5x ULN is acceptable if bilirubin is fractionated and direct bilirubin < 35%)
   • Total white blood cell count < 2,500/mm3; subjects with lymphocyte count less than the Lower Limit of Normal (LLN) may be included at the Investigator's discretion; platelet count < 95,000/mm3
   • Creatinine > 2x ULN, calculated creatinine clearance < 60 mL/min (per Cockcroft & Gault)
   • International Normalized Ratio (INR) larger than upper limit of the normal reference range (0.9 - 1.3)
3. Current chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
4. Unable to refrain from the use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (including St John's Wort) within 14 days or 5 half-lives (whichever is longer) prior to screening, unless in the opinion of the Investigator the medication will not interfere with the study procedures or compromise subject safety.
5. Previous exposure to any chimeric, humanized, or human monoclonal antibody, whether licensed or investigational.
6. Using tobacco products, nicotine products (patches, gum etc.) within 6 months prior to screening.

IPF Subjects only

1. A positive test for Human Immunodeficiency Virus (HIV) antibody, or Hepatitis C antibody result within 3 months of screening.

2. Abnormal baseline blood tests exceeding any of the limits defined below:

   • ALT or aspartate transaminase (AST) > 2x ULN, ALP and bilirubin > 2x ULN (isolated bilirubin > 2x ULN is acceptable if bilirubin is fractionated and direct bilirubin < 35%)
   • Total white blood cell count < 2,500/mm3; subjects with lymphocyte count less than the Lower Limit of Normal (LLN) may be included at the Investigator's discretion; platelet count < 95,000/mm3
   • Creatinine > 2x ULN, calculated creatinine clearance < 60 mL/min (per Cockcroft & Gault)
   • International Normalized Ratio (INR) larger than upper limit of the normal reference range (0.9 - 1.3)
3. Interstitial lung disease other than IPF.
4. Medical conditions, e.g., recent MI/stroke, severe chronic heart failure, pulmonary hypertension, or cancers, unsuitable for the study in the opinion of Investigator.
5. Acute IPF exacerbation during Screening.
6. Relevant airways obstruction (pre-bronchodilator FEV1/FVC< 0.7).
7. History of allergic or anaphylactic reaction to human, humanized, chimeric or murine monoclonal antibodies.
8. Treatment with prescription drugs for IPF within 5 half-lives of the drug, whichever is longer, prior to dosing.
9. Major surgery (major according to the investigator's assessment) planned during the course of the trial. (Being on a transplant list is allowed).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Sequential Assignment
• Masking: Triple

Number of Arms

4

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Placebo Comparator: Part A 1 (1 mg/kg HuL001); 6 healthy subjects will be enrolled and randomized to receive 1 dose of HuL001 (n = 4) or 1 dose of placebo (n = 2).	Drug: HuL001; Anti-ENO1 monoclonal antibody; Other Names: Anti-Enolase 1 monoclonal antibody
Placebo Comparator: Part A 2 (3 mg/kg HuL001); 6 healthy subjects will be enrolled and randomized to receive 1 dose of HuL001 (n = 4) or 1 dose of placebo (n = 2).	Drug: HuL001; Anti-ENO1 monoclonal antibody; Other Names: Anti-Enolase 1 monoclonal antibody
Placebo Comparator: Part A 3 (5 mg/kg HuL001); 6 healthy subjects will be enrolled and randomized to receive 1 dose of HuL001 (n = 4) or 1 dose of placebo (n = 2).	Drug: HuL001; Anti-ENO1 monoclonal antibody; Other Names: Anti-Enolase 1 monoclonal antibody
Experimental: Part B 1 (Selected Dose); At the end of Part A, the SRC will review the accumulated unblinded data of safety, tolerability, PK (any available data), and immunogenicity (any available data) to select a dose to initiate Part B in IPF subjects. Part B will be conducted in multiple-dose, uncontrolled, and open-label manner to explore the safety, tolerability, PK, and immunogenicity in IPF subjects. Only one cohort will be enrolled to receive 3 repeated doses of the selected HuL001 dose, which will be administered bi-weekly. A total of 6 IPF subjects will be enrolled in this multiple-dose cohort.	Drug: HuL001; Anti-ENO1 monoclonal antibody; Other Names: Anti-Enolase 1 monoclonal antibody

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change from baseline in hematology assessments	The hematology assessments including hematocrit, hemoglobin, platelet count, red blood cell (RBC) count, white blood cell (WBC) count (total and differential), reticulocyte count and absolute neutrophil count.	70 Days in Part A and 84 Days in Part B
Change from baseline in biochemistry assessments	The biochemistry assessments including alanine aminotransferase (ALT), albumin, alkaline phosphatase (ALP), amylase, aspartate aminotransferase (AST), bicarbonate, blood urea nitrogen (BUN), calcium, chloride, creatinine, creatinine kinase, gamma glutamyl transferase (GGT), glucose, lactic acid dehydrogenase (LDH), lipid panel (low and high density lipids cholesterol, triglycerides; total cholesterol), magnesium, potassium, sodium, total bilirubin, total protein and uric acid.	70 Days in Part A and 84 Days in Part B
Frequency, severity, and causality of adverse events (AEs), including solicited local AEs	Frequency, severity, and causality of adverse events (AEs), including solicited local AEs	70 Days in Part A and 84 Days in Part B
Proportion of subjects who report clinically significant abnormal findings in physical examination	Proportion of subjects who report clinically significant abnormal findings in physical examination	70 Days in Part A and 84 Days in Part B
Change from baseline in respiratory rate	Change from baseline in respiratory rate	70 Days in Part A and 84 Days in Part B
Change from baseline in heart rate	Change from baseline in heart rate	70 Days in Part A and 84 Days in Part B
Change from baseline in body temperature	Change from baseline in body temperature	70 Days in Part A and 84 Days in Part B
Change from baseline in electrocardiogram (ECG) results (including PR, QRS, QT, QTcF, and RR intervals)	Change from baseline in electrocardiogram (ECG) results	70 Days in Part A and 84 Days in Part B
Tolerability of HuL001 in terms of frequency of events meeting the intra-cohort stopping criteria within the tolerability observation period	Tolerability of HuL001 in terms of frequency of events meeting the intra-cohort stopping criteria within the tolerability observation period	70 Days in Part A and 84 Days in Part B
Change from baseline in blood pressure	Change from baseline in systolic and diastolic blood pressure	70 Days in Part A and 84 Days in Part B

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects- maximum observed concentration (Cmax)	PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects- maximum observed concentration (Cmax)	70 Days in Part A and 84 Days in Part B
PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects-time to reach Cmax (tmax)	PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects-time to reach Cmax (tmax)	70 Days in Part A and 84 Days in Part B
PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects- area under the curve from zero up to time t (AUC0-t)	PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects- area under the curve from zero up to time t (AUC0-t)	70 Days in Part A and 84 Days in Part B
PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects- apparent total clearance of the drug from plasma (CL/F)	PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects- apparent total clearance of the drug from plasma (CL/F)	70 Days in Part A and 84 Days in Part B
PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects- terminal half-life (t1/2)	PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects- terminal half-life (t1/2)	70 Days in Part A and 84 Days in Part B
PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects- apparent volume of distribution during terminal phase (Vz/F)	PK of single ascending doses of HuL001 in healthy subjects and multiple doses of HuL001 in IPF subjects- apparent volume of distribution during terminal phase (Vz/F)	70 Days in Part A and 84 Days in Part B
Proportion of subjects with positive anti-HuL001 antibodies	Proportion of subjects with positive anti-HuL001 antibodies	70 Days in Part A and 84 Days in Part B
Change from baseline in serum levels of cytokines	Change from baseline in serum levels of cytokines	70 Days in Part A and 84 Days in Part B

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Mean percent change from baseline of migrated PBMCs after single dose of HuL001 in healthy subjects (Cohort 1 of Part A only) and after the first and third doses of HuL001 administration in IPF subjects (Part B).	Mean percent change from baseline of migrated PBMCs after single dose of HuL001 in healthy subjects (Cohort 1 of Part A only) and after the first and third doses of HuL001 administration in IPF subjects (Part B).	0 Days in Part A and 0 Days,28 Days in Part B

Collaborators and Investigators

• Sponsor: HuniLife Biotechnology, Inc.
• Investigators: Principal Investigator: Hao-Chien Wang, MD, National Taiwan University Hospital

Study record dates

Study Major Dates

• Study Start (Actual): August 31, 2021
• Primary Completion (Anticipated): September 30, 2023
• Study Completion (Anticipated): December 31, 2023

Study Registration Dates

• First Submitted: August 25, 2020
• First Submitted That Met QC Criteria: September 1, 2020
• First Posted (Actual): September 7, 2020

Study Record Updates

• Last Update Posted (Estimate): March 9, 2023
• Last Update Submitted That Met QC Criteria: March 7, 2023
• Last Verified: March 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Respiratory Tract Diseases; Lung Diseases; Fibrosis; Pulmonary Fibrosis; Idiopathic Pulmonary Fibrosis
• Other Study ID Numbers: HuL001-CT-101

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No