Pharmacokinetics and Pharmacodynamics Study of LBS-008 in Healthy Volunteers Aged 50-85

Healthy Volunteer Clinical Trial

Official title:

A Phase 1b, Open-Label, Parallel Single-Dose Study to Evaluate the Pharmacokinetics and Pharmacodynamics of Tinlarebant in Healthy Volunteers Aged 50-85

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05667688
• Other study ID #: LBS-008-CT06
• Status: Completed
• Phase: Phase 1
• Start date: November 28, 2022
• Est. completion date: January 18, 2023

Study information

• Verified date: February 2023
• Source: RBP4 Pty Ltd
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase 1b, parallel single-dose study to evaluate the pharmacokinetics (PK) and pharmacodynamics (PD) of Tinlarebant when administered as an oral dose to elderly healthy volunteers. This study will evaluate 2 dose levels in 2 cohorts comprising up to a total of 16 participants (8 per cohort). Dose levels will be evaluated in parallel.

Description:

This is a Phase 1b, parallel single-dose study to evaluate the pharmacokinetics (PK) and pharmacodynamics (PD) of tinlarebant when administered as an oral dose to healthy volunteers aged 50-85. Tinlarebant (previously called LBS-008) is being developed as an oral treatment to slow or halt the progression of dry age-related macular degeneration (AMD) and juvenile onset macular degeneration, known as Stargardt disease (STGD). Accumulation of lipofuscin bisretinoids in the retina is associated with several retinal degenerative diseases including dry AMD and STGD. A total of up to 16 healthy volunteers aged 50-85 are planned to be enrolled into 2 cohorts (8 participants per cohort). Participants will receive a single oral dose of tinlarebant, either 5 mg (Cohort 1) or 10 mg (Cohort 2). The total maximum study duration for participants in this study is 45 days, inclusive of visit windows. This includes a screening period of up to 27 days (Day -28 to Day -2), confinement to the clinical facility over 2 nights (Day -1 to Day 2) and 5 outpatient visits including the EOS visit or Day 15. Tinlarebant will be administered in tablet form; a single tinlarebant tablet will contain 5 mg of IP. Participants in Cohort 1 will receive 1 tinlarebant tablet (5 mg dose) and participants in Cohort 2 will receive 2 tinlarebant tablets (10 mg dose). Enrolment and dosing of participants in Cohorts 1 and 2 may occur concurrently. Healthy volunteers aged 50-85, will be screened between Day -28 and Day -2, inclusive. Participants will be admitted to the clinical facility on Day -1 with tinlarebant dosing to occur on the following day (Day 1). All participants will be dosed under fasted conditions. Participants will be confined at the clinical facility from Day -1 through to Day 2 with discharge following completion of all PK and PD blood sample collections and other scheduled assessments on Day2. If participants experience any clinically significant (CS) AEs during the confinement period, they may remain in the clinical facility for further observation at the discretion of the Principal Investigator (PI). Blood samples for PK and PD analysis will be collected pre-dose and at timepoints up to 24 hours (Day 2) post-dose during the confinement period. Participants will be required to attend the clinic as outpatients on Days 3, 4, 6 and 8 for further safety assessments, PK and PD blood sampling. Participants will then return to the clinical facility for final safety assessments at an end of study (EOS) vision Day 15.

In the event of early study termination prior to the EOS visit (Day 15), participants will be requested to attend the clinic for an early termination (ET) visit.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 15
• Est. completion date: January 18, 2023
• Est. primary completion date: January 4, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 50 Years to 85 Years

Eligibility

Key inclusion criteria:

1. Must have given written informed consent before any study-related activities are carried out and must be able to understand the full nature and purpose of the trial, including possible risks and adverse effects.

2. Healthy adult male or female, or adult male or female with a stable chronic disease or condition aged 50-85 years of age, inclusive. Adults with stable chronic disease or condition includes adults with no new diagnosis, hospitalisation or changes in medication in the 3 months prior to first dose of study drug on Day 1. Ongoing concomitant medications associated with the stable disease or condition, including over-the-counter (OTC) medications and herbal/vitamin supplements taken by volunteers, will be recorded and reviewed by the PI (or delegate) to determine whether the volunteer is suitable for inclusion in the study. In conducting this review, the PI (or delegate) must consider Exclusion Criteria 11, 12, 13 and 14.

3. The volunteer is considered by the Investigator to be in stable health

Key exclusion criteria :

1. Presence of CS cardiovascular, pulmonary, hepatic, renal, haematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, oncologic, or psychiatric disease, or any other condition that, in the opinion of the Investigator, would jeopardise the safety of the participant or the validity of the study results.

2. Had a CS new illness within 1 month prior to the screening visit, with the exception of fully resolved gastrointestinal illness at least 14 days prior to the screening visit, fully resolved minor colds (e.g., only cold and flu-like symptoms) that occurred within 1 month prior to the screening visit, and fully resolved corona virus disease 2019 (COVID-19) infections if resolved at least 14 days prior to the screening visit and 30 days prior to confinement to the clinical facility.

3. A history of uncontrolled hypertension, coronary artery disease, or any other significant cardiovascular disease.

4. A history of uncontrolled diabetes. Volunteers with fully resolved gestational diabetes will be eligible to participate in the study.

5. A history of unexplained loss of consciousness, epilepsy or other seizure disorder, or cerebrovascular disease.

Related Conditions & MeSH terms

• Dry Age-related Macular Degeneration
• Healthy Volunteer
• Macular Degeneration

Intervention

Drug:
• Tinlarebant (LBS-008)
A single dose of Tinlarebant (LBS-008) will be administered to each study participant on study Day 1.

Locations

Country	Name	City	State
Australia	Nucleus Network	Melbourne

Sponsors (2)

Lead Sponsor	Collaborator
RBP4 Pty Ltd	Belite Bio, Inc

Country where clinical trial is conducted

Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	To measure the concentration of retinol, a PD biomarker , in serum following a single oral dose of tinlarebant in healthy volunteers aged 50-85.	Serum retinol concentration for each participant will be calculated	Up to 168 hours
Primary	To measure the pharmacokinetics (PK) of tinlarebant in plasma following a single oral dose in healthy volunteers aged 50-85.	Area under the plasma concentration versus time curve from time 0 to the last time point with quantifiable concentration (AUC0-t)	Up to 168 hours
Primary	To measure the pharmacokinetics (PK) of tinlarebant in plasma following a single oral dose in healthy volunteers aged 50-85.	Area under the plasma concentration versus time curve from time 0 extrapolated to infinity (AUC0-inf)	Up to 168 hours
Primary	To measure the pharmacokinetics (PK) of tinlarebant in plasma following a single oral dose in healthy volunteers aged 50-85.	Maximum observed plasma concentration (Cmax)	Up to 168 hours
Primary	To measure the pharmacokinetics (PK) of tinlarebant in plasma following a single oral dose in healthy volunteers aged 50-85.	Time of maximum observed plasma concentration (Tmax)	Up to 168 hours
Primary	To measure the pharmacokinetics (PK) of tinlarebant in plasma following a single oral dose in healthy volunteers aged 50-85.	Apparent plasma terminal elimination half-life (t1/2)	Up to 168 hours
Primary	To measure the pharmacokinetics (PK) of tinlarebant in plasma following a single oral dose in healthy volunteers aged 50-85.	Terminal elimination rate constant (?z)	Up to 168 hours
Primary	To measure the pharmacokinetics (PK) of tinlarebant in plasma following a single oral dose in healthy volunteers aged 50-85.	Apparent total body clearance (CL/F)	Up to 168 hours
Primary	To measure the pharmacokinetics (PK) of tinlarebant in plasma following a single oral dose in healthy volunteers aged 50-85.	Apparent volume of distribution (Vz/F)	Up to 168 hours
Primary	To measure the concentrations of retinol-binding protein 4 (RBP4), a pharmacodynamic (PD) biomarker, in plasma following a single oral dose in healthy volunteers aged 50-85	Time of minimal RPB4 levels post-dose (Tmin)	Up to 168 hours
Primary	To measure the concentrations of retinol-binding protein 4 (RBP4), a pharmacodynamic (PD) biomarker, in plasma following a single oral dose in healthy volunteers aged 50-85	Maximal suppression to RBP4 expressed as minimum concentration of RBP4 (Cmin)	Up to 168 hours
Primary	To measure the concentrations of retinol-binding protein 4 (RBP4), a pharmacodynamic (PD) biomarker, in plasma following a single oral dose in healthy volunteers aged 50-85	Maximal suppression to RBP4 expressed as percent (%) of baseline concentration of RBP4 (C%bmin)	Up to 168 hours
Primary	To measure the concentrations of retinol-binding protein 4 (RBP4), a pharmacodynamic (PD) biomarker, in plasma following a single oral dose in healthy volunteers aged 50-85	Level of RBP4 at 12 hours as concentration (C12h)	Up to 168 hours
Primary	To measure the concentrations of retinol-binding protein 4 (RBP4), a pharmacodynamic (PD) biomarker, in plasma following a single oral dose in healthy volunteers aged 50-85	Level of RBP4 at 12 hours as percent of baseline concentration (C%b12h)	Up to 168 hours
Primary	To measure the concentrations of retinol-binding protein 4 (RBP4), a pharmacodynamic (PD) biomarker, in plasma following a single oral dose in healthy volunteers aged 50-85	Level of RBP4 at 24 hours as concentration (C24h)	Up to 168 hours
Primary	To measure the concentrations of retinol-binding protein 4 (RBP4), a pharmacodynamic (PD) biomarker, in plasma following a single oral dose in healthy volunteers aged 50-85	Level of RBP4 at 24 hours as percent of baseline concentration (C%b24h)	Up to 168 hours
Primary	To measure the concentrations of retinol-binding protein 4 (RBP4), a pharmacodynamic (PD) biomarker, in plasma following a single oral dose in healthy volunteers aged 50-85	Half-life for recovery of RBP4 to baseline levels (PDt1/2)	Up to 168 hours
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Incidence, type, severity, and relationship of AEs/serious AEs (SAEs), including withdrawals due to AEs;	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in vital sign measurements (systolic and diastolic blood pressure (BP))	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in vital sign measurements (heart rate (HR))	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in vital sign measurements (respiratory rate)	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in vital sign measurements (body temperature)	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in electrocardiogram (ECG) parameters (RR interval)	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in electrocardiogram (ECG) parameters (PR interval)	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in electrocardiogram (ECG) parameters (QRS width)	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in electrocardiogram (ECG) parameters (QT interval)	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in electrocardiogram (ECG) parameters (QTcB)	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in electrocardiogram (ECG) parameters (QTcF)	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in visual acuity scores	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Changes from baseline in colour vision scores	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Ocular examination assessments (slit lamp biomicroscopy)	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Ocular examination assessments (dilated ophthalmoscopy)	Up to 15 days
Secondary	To investigate the systemic and ocular safety and tolerability of a single oral dose of tinlarebant in healthy adult volunteers aged 50-85.	Ocular examination assessments (intraocular pressure)	Up to 15 days