A Study to Evaluate Single and Multiple Doses of TLC-2716 in Healthy Participants

• ClinicalTrials.gov Identifier: NCT05483998
• Recruitment Status: Active, not recruiting
• First Posted: August 2, 2022
• Last Update Posted: April 10, 2023
• Sponsor: OrsoBio, Inc
• Information provided by (Responsible Party): OrsoBio, Inc

Study Description

Brief Summary:

This phase 1 study is designed to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of TLC-2716 after single- and multiple-ascending doses in healthy subjects.

Condition or disease	Intervention/treatment	Phase
Healthy Subjects	Drug: TLC-2716; Other: Placebo	Phase 1

Detailed Description:

This study is a randomized, placebo-controlled, sponsor-unblinded, and comprised of three parts: Part A (single-ascending dose), Part B (multiple-ascending dose), and Part C (adaptive single- and/or multiple-ascending dose).

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 150 participants
• Allocation: Randomized
• Intervention Model: Sequential Assignment
• Masking: Double (Participant, Investigator)
• Masking Description: Open to Sponsor
• Primary Purpose: Treatment
• Official Title: A Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single and Multiple Ascending Doses of TLC-2716 in Healthy Subjects
• Actual Study Start Date: September 9, 2022
• Estimated Primary Completion Date: April 2023
• Estimated Study Completion Date: May 2023

Arms and Interventions

Arm	Intervention/treatment
Experimental: Part A: Single Ascending Dose (SAD); Part A will be comprised of up to 50 participants over 5 cohorts of 10. Each participant will receive a single oral dose of TLC-2716 or placebo at different dose levels (1 cohort per dose level).	Drug: TLC-2716; TLC-2716; Other: Placebo; Placebo to match
Experimental: Part B: Multiple Ascending Dose (MAD); Part B will be comprised of up to 50 healthy participants over 5 cohorts of 10. Each participant will receive 14 oral doses of TLC-2716 or placebo over 14 days (given once daily) at different dose levels (1 cohort per dose level).	Drug: TLC-2716; TLC-2716; Other: Placebo; Placebo to match
Experimental: Part C: Adaptive SAD and/or MAD; Part C is an adaptive style where the dosing level is a single- or multiple-ascending dose design. Based on safety and pharmacokinetic data from Parts A and B, doses for Part C will be chosen. Part C will be comprised of up to 50 participants over 5 cohorts of 10. Each participant will receive an oral dose of TLC-2716 or placebo at different dose levels (1 cohort per dose level).	Drug: TLC-2716; TLC-2716; Other: Placebo; Placebo to match

Outcome Measures

Primary Outcome Measures :

1. Number of subjects with treatment-emergent adverse events (TEAEs) in single ascending dose (SAD) compared to placebo [ Time Frame: Up to Day 15 ]
   TEAEs are AEs that occur following the start of treatment or AEs increasing in severity during treatment.
2. Number of subjects with clinically significant change from Baseline in vital signs in SAD [ Time Frame: Day 1-Day 4, and Follow-up (after 11 days) ]
   Vital signs include blood pressure, heart rate, respiratory rate, and temperature.
3. Number of subjects with laboratory abnormalities in SAD [ Time Frame: Up to 15 days ]
   Hematology and serum chemistry.
4. Number of subjects with electrocardiogram (ECG) abnormalities in SAD [ Time Frame: Up to 15 days ]
   12-lead ECG.
5. Number of subjects with TEAEs in multiple ascending dose (MAD) compared to placebo [ Time Frame: Up to Day 28 ]
   TEAEs are AEs that occur following the start of treatment or AEs increasing in severity during treatment.
6. Number of subjects with clinically significant change from Baseline in vital signs in MAD [ Time Frame: Day 1 - Day 3, Day 5, Day 7, Day 10, Day 14, Day 17, and Follow-up (after 11 days) ]
   Vital signs include blood pressure, heart rate, respiratory rate, and temperature.
7. Number of subjects with laboratory abnormalities in MAD [ Time Frame: Up to 28 days ]
   Hematology and serum chemistry.
8. Number of subjects with ECG abnormalities in MAD [ Time Frame: Up to 28 days ]
   12-lead ECG

Secondary Outcome Measures :

1. Plasma concentration of each dose of study drug to determine AUClast in SAD [ Time Frame: Day 1: 0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 12, 24, 48, and 72 hours post-dose ]
   AUClast is defined as the concentration of drug from time zero to the last observable concentration.
2. Plasma concentration of each dose of study drug to determine AUCinf in SAD [ Time Frame: Day 1: 0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 12, 24, 48, and 72 hours post-dose ]
   AUCinf is defined as the concentration of drug extrapolated to infinite time.
3. Plasma concentration of each dose of study drug to determine %AUCexp in SAD [ Time Frame: Day 1: 0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 12, 24, 48, and 72 hours post-dose ]
   %AUCexp is defined as the percentage of AUC extrapolated between AUClast and AUCinf.
4. Plasma concentration of each dose of study drug to determine CL/F in SAD [ Time Frame: Day 1: 0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 12, 24, 48, and 72 hours post-dose ]
   CL/F is defined as the apparent oral clearance following administration of the drug.
5. Plasma concentration of each dose of study drug to determine Cmax in SAD [ Time Frame: Day 1: 0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 12, 24, 48, and 72 hours post-dose ]
   Cmax is defined as the maximum concentration of drug.
6. Plasma concentration of each dose of study drug to determine Tmax in SAD [ Time Frame: Day 1: 0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 12, 24, 48, and 72 hours post-dose ]
   Tmax is defined as the time (observed time point) of Cmax.
7. Plasma concentration of each dose of study drug to determine Clast in SAD [ Time Frame: Day 1: 0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 12, 24, 48, and 72 hours post-dose ]
   Clast is defined as the last observable concentration of drug.
8. Plasma concentration of each dose of study drug to determine Tlast in SAD [ Time Frame: Day 1: 0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 12, 24, 48, and 72 hours post-dose ]
   Tlast is defined as the time (observed time point) of Clast.
9. Plasma concentration of each dose of study drug to determine t1/2 in SAD [ Time Frame: Day 1: 0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 12, 24, 48, and 72 hours post-dose ]
   t1/2 is defined as the estimate of the terminal elimination half-life of the drug.
10. Plasma concentration of each dose of study drug to determine λz in SAD [ Time Frame: Day 1: 0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 12, 24, 48, and 72 hours post-dose ]
    λz is defined as the terminal elimination rate constant, estimated by linear regression of the terminal elimination phase of the log plasma concentration of drug versus time curve of the drug.
11. Plasma concentration of each dose of study drug to determine AUClast in MAD [ Time Frame: Day 1, Day 3, Day 7, Day 14 ]
    AUClast is defined as the concentration of drug from time zero to the last observable concentration.
12. Plasma concentration of each dose of study drug to determine AUCtau in MAD [ Time Frame: Day 1, Day 3, Day 7, Day 14 ]
    AUCtau is the concentration of drug over time (area under the plasma concentration versus time curve over the dosing interval).
13. Plasma concentration of each dose of study drug to determine Ctau in MAD [ Time Frame: Day 1, Day 3, Day 7, Day 14 ]
    Ctau is defined as the observed drug concentration at the end of the dosing interval.
14. Plasma concentration of each dose of study drug to determine CLss/F in MAD [ Time Frame: Day 1, Day 3, Day 7, Day 14 ]
    CLss/F is the total body clearance for extravascular administration divided by the fraction of dose absorbed.
15. Plasma concentration of each dose of study drug to determine Cmax in MAD [ Time Frame: Day 1, Day 3, Day 7, Day 14 ]
    Cmax is defined as the maximum concentration of drug.
16. Plasma concentration of each dose of study drug to determine Tmax in MAD [ Time Frame: Day 1, Day 3, Day 7, Day 14 ]
    Tmax is defined as the time (observed time point) of Cmax.
17. Plasma concentration of each dose of study drug to determine Clast in MAD [ Time Frame: Day 1, Day 3, Day 7, Day 14 ]
    Clast is defined as the last observable concentration of drug.
18. Plasma concentration of each dose of study drug to determine Tlast in MAD [ Time Frame: Day 1, Day 3, Day 7, Day 14 ]
    Tlast is defined as the time (observed time point) of Clast.
19. Plasma concentration of each dose of study drug to determine t1/2 in MAD [ Time Frame: Day 1, Day 3, Day 7, Day 14 ]
    t1/2 is defined as the estimate of the terminal elimination half-life of the drug.
20. Plasma concentration of each dose of study drug to determine λz in MAD [ Time Frame: Day 1, Day 3, Day 7, Day 14 ]
    λz is defined as the terminal elimination rate constant, estimated by linear regression of the terminal elimination phase of the log plasma concentration of drug versus time curve of the drug.

Eligibility Criteria

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

Criteria

Inclusion Criteria:

• Non-smoking, healthy male or female subject between 18 and 55 years of age, inclusive
• Body mass index from 19 to 35 kg/m2, inclusive
• Estimated glomerular filtration rate ≥ 80 mL/min
• Normal liver biochemistry tests
• Screening laboratory evaluations (hematology, chemistry, and urinalysis) must fall within the normal range of the local laboratory's reference ranges unless the results have been determined by the investigator to have no clinical significance
• Subject must have either a normal 12-lead electrocardiogram (ECG) or one with abnormalities that are considered clinically insignificant by the investigator
• Females of childbearing potential must have a negative pregnancy test at Screening and clinic admission
• Male subjects and female subjects of childbearing potential who engage in heterosexual intercourse must agree to use protocol-specified method(s) of contraception
• Must, in the opinion of the investigator, be in good health based upon medical history and physical examination, including vital signs

Exclusion Criteria:

• Pregnant or lactating subjects
• Subjects with triglycerides ≥ 500 mg/dL
• Subjects with low-density lipoprotein ≥ 190 mg/dL
• Subjects who have any serious or active medical or psychiatric illness (including depression) that, in the opinion of the investigator, would interfere with the subject's treatment, assessment, or compliance with the protocol
• Subjects who have received any investigational compound within 30 days or 5 half-lives, whichever is longer, prior to study drug dosing
• Current alcohol abuse that is judged by the investigator to potentially interfere with the subject's compliance or safety
• Current substance abuse that is judged by the investigator to potentially interfere with the subject's compliance or safety
• A positive test result for human immunodeficiency virus (HIV-1) antibody, hepatitis B (HBV) surface antigen, or hepatitis C (HCV) antibody
• Subjects who have taken any prescription medications or over-the-counter medications, including herbal products, within 28 days prior to start of study drug dosing, with the exception of vitamins, acetaminophen (paracetamol), ibuprofen, and/or hormonal contraceptive medications
• Subjects who have been treated with systemic steroids, immunosuppressant therapies, or chemotherapeutic agents within 3 months prior to Screening or expected to receive these agents during the study (e.g., corticosteroids, immunoglobulins, and other immune- or cytokine-based therapies)
• Medical history of serious skin disease in the opinion of the investigator, such as but not limited to rash, food allergy, eczema, psoriasis, or urticaria
• Medical history of drug sensitivity or drug allergy (such as anaphylaxis or hepatoxicity)
• Presence or history of cardiovascular disease, including significant cardiovascular disease (including a history of myocardial infarction based on ECG and/or clinical history), history of cardiac conduction abnormalities (including any history of ventricular tachycardia), congestive heart failure, cardiomyopathy with left ventricular ejection fraction < 40%, a family history of Long QT Syndrome, or unexplained death in an otherwise healthy individual between the ages of 1 and 30 years
• Syncope, palpitations, or unexplained dizziness
• Implanted defibrillator or pacemaker
• Medical history of liver disease, including but not limited to alcoholic liver disease, autoimmune disorders (e.g., primary biliary cholangitis, primary sclerosing cholangitis, autoimmune hepatitis), drug-induced hepatotoxicity, Wilson disease, clinically significant iron overload, or alpha-1-antitrypsin deficiency)
• Severe peptic ulcer disease, gastroesophageal reflux disease, or other gastric acid hypersecretory conditions
• History of medical or surgical treatment that permanently alters intestinal absorption (e.g., gastric or intestinal surgery)
• Subjects who have received vaccination for COVID-19 within 14 days of Admission

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Contacts and Locations

Locations

New Zealand

OrsoBio Research Site

Auckland, New Zealand

Sponsors and Collaborators

OrsoBio, Inc

Investigators

• Study Director: OrsoBio Study Director; OrsoBio, Inc

More Information

• Responsible Party: OrsoBio, Inc
• ClinicalTrials.gov Identifier: NCT05483998
• Other Study ID Numbers: 2716-CL-101
• First Posted: August 2, 2022
• Last Update Posted: April 10, 2023
• Last Verified: April 2023

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No