A Two-part Pharmacokinetic Study of PXS-5382A in Healthy Adult Males

NCT04183517 | Completed Phase 1 DMC

• 1 other identifier: PXS-5382A-102
• Study Type: interventional
• Target: 18
• Locations: 1 country
• Sites: 1

Brief Summary

This is a Phase I, open-label, two-part in healthy adult males. There will be up to 12 subjects with 6 subjects in each part of the study. Subjects from Part A are eligible to participate in Part B. For Part A, each of the 6 subjects will complete two periods of the study with washout period of 7 days between. Each subject during participation in the study will receive a dose of PXS 5382A orally in a fed state and a fasted state. For Part B, repeated oral BID administration of PXS-5382A will be performed in the Fed state and dose will be dependent on analysis of Part A. In both part A and B PK, PD and safety assessments will be collected.

Conditions

Pharmacokinetics

Outcome Measures

Primary Outcomes (4)

• Cmax after oral administration of PXS-5382A

  Maximum plasma concentration

  6 days

• Tmax after oral administration of PXS-5382A

  Time of the observed maximum plasma concentration

  6 days

• AUC0-inf of PXS-5382A

  Area under the plasma concentration-time curve (AUC) from time zero extrapolated to infinity

  6 days

• t1/2 of PXS-5382A

  Terminal plasma elimination half-life

  6 days

Secondary Outcomes (4)

• Maximum percentage inhibition plasma LOXL2 of PXS-5382A

  6 days

• Incidence and severity of Adverse Events

  6 days

• Number of subjects with clinical laboratory test abnormalities

  6 days

• Number of subjects with vital signs abnormalities

  6 days

Study Arms (3)

Fasted

EXPERIMENTAL

PXS-5382A administered as a single dose in the fasted state

Drug: PXS-5382A

Fed

EXPERIMENTAL

PXS-5382A administered as a single dose in the fed state

Drug: PXS-5382A

Twice daily

EXPERIMENTAL

PXS-5382A administered twice daily for 5 days in the fed state

Drug: PXS-5382A

Interventions

PXS-5382A DRUG

Orally once daily or twice daily

Fasted; Fed; Twice daily

Eligibility Criteria

• Age: 18 Years - 60 Years
• Sex: male
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Healthy males, aged between 18 and 60 years (inclusive).
• Eligibility of the subjects based on clinical history, physical examination, ECG and Lab results
• BMI between 18.5 kg/m2 and 30.0 kg/m2 inclusive.
• No clinically relevant abnormality in an ECG; QTcF (Fridericia's corrected QT) ≤ 450 ms, PR interval of 120-210 ms and a QRS duration ≤ 120 ms.
• Adequate venous access in the left or right arm to allow dosing and collection of a number of blood samples.
• Male subjects with female partners of childbearing potential may be enrolled if they:
• are documented to be surgically sterile (vasectomy at least six months prior to dosing), or
• practice true abstinence for 30 days after the study drug administration, or
• agree to use a barrier method of contraception (e.g. condom) from Screening and until 30 days after administration of the study. Additionally, the female partner must use a highly effective hormonal method, such as birth control pills, patches, implants or injections; or used an intra uterine device (IUD).
• Contraceptive requirements do not apply to subjects who are exclusively in same-sex relationships.
• Have given written informed consent to participate in this study in accordance with local regulations.

You may not qualify if:

• Clinically significant abnormal findings on the physical examination, medical history, ECG or laboratory results as deemed by the PI (or delegate).
• Clinically significant gastrointestinal, renal, hepatic, neurologic, haematologic (including thalassaemia), endocrine, oncologic, pulmonary, immunologic, psychiatric, skin or cardiovascular disease or any other condition, which, in the opinion of the PI (or delegate), would jeopardise the safety of the subject or impacted the validity of the study results.
• History of significant drug allergies or significant allergic reaction or suffer from clinically significant systemic allergic disease. Mild hay fever is acceptable.
• Evidence of abnormal wound healing (e.g. hypertrophic scars) as the result of surgery or trauma as deemed by the PI or delegate.
• Have received or are anticipated to receive any prescription systemic or topical medication, or any over the counter, supplements, complementary or alternative medicine 7 days prior to the start of dosing or within 5 half-lives of the drug whichever is longer (excluding paracetamol).
• Systolic BP \< 90 or \> 140 mmHg, diastolic BP \< 40 or \> 90 mmHg and HR \< 40 or \> 100 beats per minute (BPM).
• ALT, AST or total bilirubin \> 1.5x ULN.
• Gilbert's syndrome sufferers are not eligible.
• Evidence of significant renal insufficiency, as indicated by an estimated creatinine clearance using the Cockcroft-Gault formula of less than 80 mL/min at Screening.
• Positive Screening test for Hepatitis B surface antigen or Hepatitis C antibody or human immunodeficiency virus (HIV)
• Any condition directly or indirectly caused by or associated with Transmissible Spongiform Encephalopathy (TSE) Creutzfeldt-Jakob Disease (CJD) variant Creutzfeldt-Jakob Disease (vCJD) or new variant Creutzfeldt-Jakob Disease (nvCJD)
• History of drug abuse in the last 2 years.
• Males who regularly drink more than four (4) units of alcohol daily (1 unit = 285 mL beer (4.9% Alc./Vol), 100 mL wine (12% Alc./Vol), 30 mL spirit (40% Alc./Vol)).
• Use nicotine-containing products (e.g., cigarettes, e-cigarettes, cigars, chewing tobacco, snuff) within 6 weeks before screening and were unable to abstain from using these products until study completion.
• Unable to abstain from consuming caffeine and/or xanthine products (i.e., coffee, tea, chocolate, and caffeine-containing sodas, colas, etc.) for defined periods (eg, to the clinical facility).

Sponsors & Collaborators

• Syntara: lead

Study Sites (1)

CMAX

Adelaide, Australia

Location

Study Officials

• Angela Molga, MBBS

  CMAX Ltd

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 26, 2019
• First Posted: December 3, 2019
• Study Start: December 20, 2019
• Primary Completion: April 4, 2020
• Study Completion: June 24, 2020
• Last Updated: June 25, 2020

Record last verified: 2020-06

Data Sharing

• IPD Sharing: Will not share

Locations

AU (1)