None listed
Conditions
Brief summary
The research project is testing a potential new treatment for Idiopathic pulmonary fibrosis (IPF), called FTP-198. Before a new medicine can be approved for use in humans, it is necessary to confirm that it is safe and effective. Although laboratory and animal studies have been completed, this is the first time FTP-198 is being tested in humans. Therefore, side effects in human are unknown. Thus, the purpose of this study is to evaluate the safety and tolerability of single and multiple doses of FTP-198. The pharmacokinetics (PK) of FTP-198 in humans will also be determined. PK testing involves taking blood samples to measure how much of the drug gets into the blood stream, and how long the body takes to remove it or excrete it. When testing for PK, your sample will also be tested to determine the amount of LPA in your blood. This is called a pharmacodynamic (PD) parameter.
Interventions
A suspension of FTP-198 in a sugar-free, alcohol-free syrup vehicle (ORA-Sweet SF) will be administered to participants.
Part A: FTP-198 will be administered at the following nominal dose levels in each cohort:
• Cohort 1 - 50 mg
• Cohort 2 - 100 mg
• Cohort 3 - 200 mg
• Cohort 4 - 300 mg
• Cohort 5 - 450 mg
• Cohort 6 - 600 mg
Part B: It is anticipated that FTP-198 at 3 dose levels in the range of 50 to 600 mg will be evaluated in 3 cohorts (Cohorts 7 to 9). The dose levels to be administer
A suspension of FTP-198 in a sugar-free, alcohol-free syrup vehicle (ORA-Sweet SF) will be administered to participants. Part A: FTP-198 will be administered at the following nominal dose levels in each cohort: • Cohort 1 - 50 mg • Cohort 2 - 100 mg • Cohort 3 - 200 mg • Cohort 4 - 300 mg • Cohort 5 - 450 mg • Cohort 6 - 600 mg Part B: It is anticipated that FTP-198 at 3 dose levels in the range of 50 to 600 mg will be evaluated in 3 cohorts (Cohorts 7 to 9). The dose levels to be administered will be decided following review of safety and PK data from Part A. Part A: 1 dose. Part B: There will be a total of 7 dosing days. Depending on PK data from Part A, each daily dose may be administered once daily or twice daily. Adherence to the intervention will be monitored via direct supervision of the intake of suspension by the CMAX staff.
Sponsors
Avance Clinical
Study design
Allocation
Randomised controlled trial
Intervention model
Other
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
All
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
Healthy volunteers will be included in Part A or Part B of the study if they satisfy all the following 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. Adult males and females, 18 to 55 years of age (inclusive) at screening; 3. Body mass index greater than or equal to 18.0 and less than or equal to 30.0 kg/m2, with a body weight greater than or equal to 50 kg at screening; 4. Be nonsmokers (including tobacco, e-cigarettes and marijuana) for at least 1 month prior to first study drug administration; 5. Medically healthy without clinically significant abnormalities at screening and pre dose on Day 1, including: a. Physical examination without any clinically relevant findings; b. Systolic blood pressure in the range of 90 to 160 mmHg and diastolic blood pressure in the range of 50 to 95 mmHg after 5 minutes in supine position; c. Heart rate in the range of 50 to 100 bpm after 5 minutes rest in supine position; d. Body temperature, between 35.0°C and 37.5°C; e. No clinically significant findings in serum chemistry, hematology, coagulation and urinalysis tests as judged by the investigator; 6. Conventional 12-lead ECG recording in triplicate (the mean of triplicate measurements will be used to determine eligibility at screening and predose on Day 1) consistent with normal cardiac conduction and function, including: • Normal sinus rhythm with HR between 50 and 100 bpm, inclusive; • QT interval corrected using the Fridericia method (QTcF) between 350 to 450 msec for male subjects and 350 to 470 msec for female subjects, inclusive; • QRS duration of less than 120 msec; • PR interval of less than or equal to 210 msec; • Electrocardiogram morphology consistent with healthy cardiac ventricular conduction and normal rhythm, and with measurement of the QT interval; • No family history of short or long QT syndrome; • No history of risk factors for torsade de pointes or the diagnosis; 7. Female participants must: a. Be of nonchildbearing potential ie, surgically sterilized (hysterectomy, bilateral salpingectomy, bilateral oophorectomy at least 6 weeks before screening) or postmenopausal (where postmenopausal is defined as no menses for 12 months without an alternative medical cause), or b. If of childbearing potential, must have a negative pregnancy test at screening (blood test) and before the first study drug administration (Day -1 urine test). They must agree not to attempt to become pregnant, must not donate ova, and must use a highly effective contraceptive method from signing the consent form until at least 30 days after the last dose of study drug. 8. Male participants, if not surgically sterilized, must be willing not to donate sperm and, if engaging in sexual intercourse with a female partner who could become pregnant, must be willing to use a condom in addition to having the female partner use a highly effective contraceptive method from signing the consent form until at least 90 days after the last dose of study drug; 9. Have suitable venous access for blood sampling; 10. Be willing and able to comply with all study assessments and adhere to the protocol schedule and restrictions.
Exclusion criteria
Healthy volunteers will be excluded from Part A or Part B of the study if there is evidence of any of the following at screening, Day -1 or pre dose on Day 1: 1. History or presence of significant cardiovascular, pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine, immunologic, dermatologic or neurological disease, including any acute illness or surgery within the past 3 months determined by the PI to be clinically relevant; 2. Current infection that requires antibiotic, antifungal, antiparasitic or antiviral medications; 3. Any history of malignant disease in the last 10 years (excludes surgically resected skin squamous cell or basal cell carcinoma); 4. Presence of clinically relevant immunosuppression from, but not limited to, immunodeficiency conditions such as common variable hypogammaglobulinemia; 5. Use of or plans to use systemic immunosuppressive (eg, corticosteroids, methotrexate, azathioprine, cyclosporine) or immunomodulating medications (eg, interferon) during the study or within 4 months prior to the first study drug administration; 6. Liver function test results (ie, aspartate aminotransferase [AST], alanine aminotransferase [ALT], and gammaglutamyl transferase [GGT]) and total bilirubin must not be elevated more than 1.2-fold above the upper limit of normal (ULN); 7. Positive test results for active human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg) or hepatitis C virus (HCV) antibodies (Abs); 8. History of active, latent or inadequately treated tuberculosis infection; 9. Presence or having sequelae of gastrointestinal, liver, kidney, or other conditions known to interfere with the absorption, distribution, metabolism, or excretion of drugs; 10. Estimated creatinine clearance (CrCl) < 40 mL/min using the Cockcroft-Gault formula or serum creatinine more than 1.5-fold above the ULN; 11. History of substance abuse or alcohol abuse within 12 months prior to first study drug administration; 12. Positive drug or alcohol test results; 13. Use of any prescription or over-the-counter medication (including herbal products, diet aids, and hormone supplements) within 10 days or 5 half-lives of the medication (whichever is longer) prior to the first study drug administration, except occasional use of paracetamol; 14. Demonstrated clinically significant (required intervention, eg, emergency room visit, epinephrine administration) allergic reactions (eg, food, drug, or atopic reactions, asthmatic episodes) which, in the opinion of the investigator, would interfere with the volunteer’s ability to participate in the trial; 15. Known hypersensitivity to any of the study drug ingredients; 16. Use of any live vaccinations within 30 days prior to the first study drug administration except for the influenza vaccine; 17. For women of childbearing potential, a positive serum pregnancy test at screening or a positive urine pregnancy test with confirmatory serum pregnancy test on Day -1; 18. Donation of blood or plasma within 30 days prior to first study drug administration, or loss of whole blood of more than 500 mL within 30 days prior to randomization, or receipt of a blood transfusion within 1 year of first study drug administration; 19. Participation in another investigational clinical trial within 60 days prior to the first study drug administration; 20. Any other condition or prior therapy that in the opinion of the PI would make the volunteer unsuitable for this study, including inability to cooperate fully with the requirements of the study protocol or likelihood of noncompliance with any study requirements; 21. Is an employee of an investigator or sponsor or an immediate relative of an investigator.
Outcome results
None listed