Multiple-Dose, Dose-Escalation Study to Evaluate the Safety/Tolerability and Pharmacokinetics of FP-045

NCT03686930 | Completed Phase 1 DMC

• 1 other identifier: FP045C-17-001
• Study Type: interventional
• Target: 24
• Locations: 1 country
• Sites: 1

Brief Summary

Phase I, single-center, randomized, double-blind, placebo-controlled, multiple ascending dose (MAD), study to evaluate the safety/tolerability and pharmacokinetics (PK) of FP-045 administered to normal health volunteers (NHVs). 3 cohorts of NHVs will be enrolled. Subjects in each cohort will be randomized to orally receive either FP-045 (6 subjects) or placebo (2 subjects). Subjects will receive 7 daily doses of study drug. Subjects will be screened for study eligibility within 21 days before Day 1 and will have been admitted to the CRU on Day -1 to confirm eligibility and to undergo baseline assessments. Subjects will remain in the CRU for observation until completion of all assessments on Day 10. Subjects will return to the CRU on Day 11 for an additional PK sample, and again for an end of study (EOS) Visit on Day 14 (±2 days) for safety evaluations and collection of PK samples.

Conditions

Healthy Volunteers

Outcome Measures

Primary Outcomes (9)

• Change in baseline measures for vital sign parameters [safety/tolerability]

  Outcome Measures units of measure include weight in kilograms.

  14 days ± 2 days

• Change in baseline measures for ECG parameters [safety/tolerability]

  T wave

  14 days ± 2 days

• Change in baseline measures for clinical laboratory test [safety/tolerability]

  Number of Participants with Abnormal Laboratory Values. Blood will be drawn to measure the chemistry of the blood prior to and after dosing.

  14 days ± 2 days

• Number of participants with treatment-emergent ECG abnormalities [safety/tolerability].

  14 days ± 2 days

• Number of participants with treatment-emergent AEs [safety/tolerability].

  14 days ± 2 days

• Number of participants with treatment-emergent AEs leading to premature discontinuation of study drug [safety/tolerability].

  14 days ± 2 days

• Number of participants with treatment-emergent SAEs [safety/tolerability].

  14 days ± 2 days

• Change in baseline measures for vital sign parameters [safety/tolerability]

  Outcome Measures units of measure include height in meters.

  14 days ± 2 days

• Change in baseline measures for vital sign parameters [safety/tolerability]

  Outcome Measures units of measure include blood pressure both systolic and diastolic will be measured.

  14 days ± 2 days

Secondary Outcomes (10)

• Pharmacokinetic (PK) profile (Cmax) following multiple, escalating oral doses of FP-045.

  14 days ± 2 days

• Pharmacokinetic (PK) profile (Tmax) following multiple, escalating oral doses of FP-045.

  14 days ± 2 days

• Pharmacokinetic (PK) profile (AUC0-24) following multiple, escalating oral doses of FP-045.

  14 days ± 2 days

• Pharmacokinetic (PK) profile (Cavg) following multiple, escalating oral doses of FP-045.

  14 days ± 2 days

• Pharmacokinetic (PK) profile (accumulation ratio of AUC0-24) following multiple, escalating oral doses of FP-045.

  14 days ± 2 days

Study Arms (6)

Cohort 1 - FP-045 oral solution

ACTIVE COMPARATOR

FP-045 powder for oral solution, will be reconstituted once daily (QD) dose, administered for 7 consecutive days.

Drug: Cohort 1 - FP-045 oral solution

Cohort 1 - Placebo for FP-045 oral solution

PLACEBO COMPARATOR

Placebo oral solution that is identical to the test product, but without FP-045.

Drug: Placebo (for FP-045 oral solution)

Cohort 2 - FP-045 oral solution

ACTIVE COMPARATOR

FP-045 powder for oral solution (escalated dose), will be reconstituted once daily (QD) dose, administered for 7 consecutive days.

Drug: Cohort 2 - FP-045 oral solution

Cohort 2 - Placebo for FP-045 oral solution

PLACEBO COMPARATOR

Placebo oral solution that is identical to the test product, but without FP-045.

Drug: Placebo (for FP-045 oral solution)

Cohort 3 - FP-045 oral solution

ACTIVE COMPARATOR

FP-045 powder for oral solution (escalated dose), will be reconstituted once daily (QD) dose, administered for 7 consecutive days.

Drug: Cohort 3 - FP-045 oral solution

Cohort 3 - Placebo for FP-045 oral solution

PLACEBO COMPARATOR

Placebo oral solution that is identical to the test product, but without FP-045.

Drug: Placebo (for FP-045 oral solution)

Interventions

Cohort 1 - FP-045 oral solution DRUG

FP-045 given orally with dose escalation between cohorts, based on emerging safety and pharmacokinetic (PK) data. Cohorts 2 and 3 doses to be based on the safety, tolerability, and PK data generated in the study. The dosing duration for cohorts 1-3 will be 7 consecutive days.

Cohort 1 - FP-045 oral solution

Cohort 2 - FP-045 oral solution DRUG

FP-045 given orally with dose escalation between cohorts, based on emerging safety and pharmacokinetic (PK) data. Cohorts 2 and 3 doses to be based on the safety, tolerability, and PK data generated in the study. The dosing duration for cohorts 1-3 will be 7 consecutive days.

Cohort 2 - FP-045 oral solution

Cohort 3 - FP-045 oral solution DRUG

FP-045 given orally with dose escalation between cohorts, based on emerging safety and pharmacokinetic (PK) data. Cohorts 2 and 3 doses to be based on the safety, tolerability, and PK data generated in the study. The dosing duration for cohorts 1-3 will be 7 consecutive days.

Cohort 3 - FP-045 oral solution

Placebo (for FP-045 oral solution) DRUG

Participants (cohorts 1-3) will receive FP-045 oral solution matching placebo.

Cohort 1 - Placebo for FP-045 oral solution; Cohort 2 - Placebo for FP-045 oral solution; Cohort 3 - Placebo for FP-045 oral solution

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Male or female NHV, age 18 to 55 years, inclusive (at the time of informed consent).
• Females must be either postmenopausal for ≥1 year (or with FSH ≥ 40 mIU/mL if postmenopausal for \< 1 year) or surgically sterile (having undergone bilateral tubal ligation, hysterectomy, or bilateral oophorectomy) for at least 6 months.
• Males with female partners of childbearing potential must agree to use barrier contraceptive (i.e., condom) and their female partners must use a highly effective method of contraception from Screening through 90 days after the last dose of study drug. Males must also refrain from sperm donations during this time period.
• Males who are abstinent will not be required to use a contraceptive method unless they become sexually active.
• The subject is, in the opinion of the Investigator, generally healthy based on assessment of medical history, physical examination, vital signs, electrocardiogram (ECG), and the results of the hematology, clinical chemistry, urinalysis, serology, and other laboratory tests.
• Baseline laboratory test values within reference ranges based on the blood and urine samples taken at Screening and on Day -1 (before administration of the initial study drug). Out of normal ranges values may be accepted by the Investigator, if not clinically significant.
• Nonsmoker and/or ex-smoker who has discontinued smoking and/or use of nicotine containing products for at least 6 months prior to the first dose of study drug
• Body mass index between 18 and 30 kg/m2, inclusive
• Written informed consent obtained Ability to communicate well with the Investigator, in the local language, and to understand and comply with the requirements of the study.

You may not qualify if:

• History or presence of any clinically significant neurological, metabolic, gastrointestinal, endocrinological (in particular diabetes or pre-diabetes), cardiovascular, hematological, hepatic, immunological, renal, respiratory, chronic infections, psychiatric, or genitourinary abnormalities or diseases. Note: NHVs with a history of uncomplicated kidney stones or asthma may be enrolled in the study at the discretion of the Investigator.
• History of malignant neoplastic disease, with the following exceptions:
• Adequately treated non-melanomatous skin carcinoma
• Female with a history of benign cervical carcinoma neoplasia if compliant with surveillance and treatment as recommended by her physician
• Mentally or legally incapacitated, has significant emotional problems at Screening or expected during the conduct of the study, or has a history of a clinically significant psychiatric disorder within the last 5 years. Note: NHVs who have had situational depression may be enrolled in the study at the discretion of the Investigator.
• The subject has a history of severe drug allergy or hypersensitivity or food allergy, including anaphylaxis.
• The subject has had surgery or trauma with significant blood loss within the last 3 months prior to the first dose of study drug.
• The subject has donated blood more than 1 unit (500 mL) with 4 weeks prior to the first dose of study drug.
• Fever (body temperature \>38°C) or symptomatic viral or bacterial infection within 2 weeks prior to Screening
• Blood pressure \>140/90 mm Hg or heart rate \>100 beats per minute at Screening or at Day -1. Vitals may be repeated up to 2 times for the purpose of eligibility.
• Clinically significant laboratory abnormalities including:
• Impaired renal function (serum creatinine levels \>ULN) at Screening; estimated creatinine clearance (CrCl) of \<80 mL/min
• Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) laboratory values \>1.2 × upper normal limits
• Clinically significant abnormality on ECG performed at Screening or prior to administration of the initial dose of study drug. (Screening ECG conduction intervals must be 10. Clinically significant abnormality on ECG performed at Screening or prior to administration of the initial dose of study drug. (Screening ECG conduction intervals must be within gender specific normal ranges \[QT interval corrected for heart rate \[QTc\] males ≤450 msec and females ≤470 msec\].)
• Positive test for hepatitis C antibody, hepatitis B surface antigen, or human immunodeficiency virus antibody at Screening

Sponsors & Collaborators

• Foresee Pharmaceuticals Co., Ltd.: lead

Study Sites (1)

Nucleus Networks

Melbourne, Australia

Location

Study Officials

• David Lau, Ph.D.

  Foresee Pharma

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
• Masking Details: double-blind, placebo-controlled
• Purpose: TREATMENT
• Intervention Model: SEQUENTIAL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Multiple Dose, Dose Escalation study

Study Record Dates

• First Submitted: April 10, 2018
• First Posted: September 27, 2018
• Study Start: February 22, 2018
• Primary Completion: May 27, 2018
• Study Completion: August 10, 2018
• Last Updated: April 29, 2022

Record last verified: 2022-04

Locations

AU (1)