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Safety and Tolerability Study of LBS-008 in Healthy Adult Subjects After Single and Multiple Doses

Phase 1
Completed
Conditions
Healthy Volunteer
Interventions
Drug: Placebos
Registration Number
NCT03735810
Lead Sponsor
RBP4 Pty Ltd
Brief Summary

This is a single center, randomized, double-blind, placebo-controlled, Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) study is planned to assess safety, pharmacokinetics (PK), and pharmacodynamics of LBS-008 in healthy adult volunteers.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
71
Inclusion Criteria
  • The subject is male or female, 18 to 65 years of age, inclusive, at screening.
  • The subject voluntarily consents to participate in this study and provides written informed consent before the start of any study-specific procedures.
  • The subject is willing and able to remain in the study unit for the entire duration of the confinement period and return for outpatient visits.
  • Female subjects must be of nonchildbearing potential (defined as surgically sterile [i.e., had a bilateral tubal ligation, hysterectomy, or bilateral oophorectomy at least 6 months before the dose of study drug] or postmenopausal for at least 1 year before study drug administration confirmed by FSH test at screening; FSH level >40 mIU/mL). Female subjects may also be considered of non-childbearing if they have a confirmed medical condition which would deem the subject as infertile. E.g. MRKH Syndrome (Mullerian Agenesis) or another applicable condition.
  • Male subjects must be surgically sterile (i.e., vasectomy) for at least 3 months before screening; or remain abstinent or agree to use a highly effective form of contraception when sexually active with a female partner for 90 days after study drug administration. Highly effective contraception requires use of a condom and appropriate contraceptive measures for your female partner (i.e. oral, injected or implanted hormonal methods, or placement of an intrauterine device or intrauterine system). This requirement does not apply to subjects in a same sex relationship and female partners of non-childbearing potential.
  • The subject has a body mass index (BMI) of 18 to 30 kg/m2, inclusive, and weighs 50 to 100 kg (110 to 220 pounds), inclusive, at screening and check-in.
  • The subject is considered to be in stable health by the investigator.
  • The subject agrees to comply with all protocol requirements.
Exclusion Criteria
  • Any significant acute or chronic medical illness including history or presence of clinically significant cardiovascular, pulmonary, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, oncologic, or psychiatric disease
  • Vitamin A deficiency.
  • Any recent viral or bacterial infection.
  • Participated in any clinical study in last 6 weeks.
  • History of significant drug allergy
  • History of significant vision, ocular or retinal disorder.
  • Recent surgery, blood transfusion, drug or alcohol abuse and use of tobacco or nicotine containing products in past month.
  • Evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, ECGs, or clinical laboratory determinations Other protocol-defined inclusion/exclusion criteria could apply.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
SAD - Cohort 4Placebos400 mg LBS-008 or placebo
SAD - Cohort 4LBS-008400 mg LBS-008 or placebo
SAD - Cohort 1LBS-00850 mg LBS-008 or placebo
SAD - Cohort 1Placebos50 mg LBS-008 or placebo
SAD - Cohort 2LBS-008100 mg LBS-008 or placebo
SAD - Cohort 2Placebos100 mg LBS-008 or placebo
SAD - Cohort 3LBS-008200 mg LBS-008 or placebo
SAD - Cohort 3Placebos200 mg LBS-008 or placebo
MAD - Cohort 1LBS-00810 mg LBS-008 or placebo
MAD - Cohort 1Placebos10 mg LBS-008 or placebo
MAD - Cohort 2Placebos25 mg LBS-008 or placebo
MAD - Cohort 3Placebos5 mg LBS-008 or placebo
MAD - Cohort 4LBS-00812 mg LBS-008 or placebo
MAD - Cohort 4Placebos12 mg LBS-008 or placebo
SAD - Cohort 5Placebos25 mg LBS-008 or placebo
SAD - Cohort 5LBS-00825 mg LBS-008 or placebo
MAD - Cohort 2LBS-00825 mg LBS-008 or placebo
MAD - Cohort 3LBS-0085 mg LBS-008 or placebo
Primary Outcome Measures
NameTimeMethod
Area under the plasma concentration versus time curve from time 0 to the last timepoint with quantifiable concentration (AUC0-t)SAD portion: Day 1 to Day 8; MAD portion: Day 1 to Day 28
Area under the plasma concentration versus time curve from time 0 extrapolated to infinity (AUC0-inf)SAD portion: Day 1 to Day 8; MAD portion: Day 1 to Day 28
Maximum observed plasma concentration (Cmax)SAD portion: Day 1 to Day 6; MAD portion: Day 1 to Day 28
Time to maximum observed plasma concentration (Tmax)SAD portion: Day 1 to Day 8; MAD portion: Day 1 to Day 28
Terminal elimination rate constantSAD portion: Day 1 to Day 8; MAD portion: Day 1 to Day 28
Terminal phase half-life (t1/2)SAD portion: Day 1 to Day 8; MAD portion: Day 1 to Day 28
Apparent total body clearance (CL/F)SAD portion: Day 1 to Day 8; MAD portion: Day 1 to Day 28
Apparent volume of distribution (Vz/F)SAD portion: Day 1 to Day 8; MAD portion: Day 1 to Day 28
Number of participants with Adverse Events (AEs), Serious Adverse Events (SAEs) and AEs leading to discontinuation.SAD portion: Day 1 to Day 8; MAD portion: Day 1 to Day 28
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Linear Clinical Research

🇦🇺

Perth, Australia

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