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Clinical Trials/NCT05625334
NCT05625334
Completed
Phase 1

A Single-dose, Open-label, Randomized, Multi-center, 2-treatment Crossover Study to Compare the Pharmacodynamics, Pharmacokinetics, Safety, and Tolerability of Acetylsalicylic Acid Powder for Oral Inhalation With Non-enteric-coated Chewable Aspirin in Healthy Adults

Vectura, Inc.2 sites in 1 country86 target enrollmentOctober 14, 2022

Overview

Phase
Phase 1
Intervention
ASA
Conditions
Healthy Volunteers
Sponsor
Vectura, Inc.
Enrollment
86
Locations
2
Primary Endpoint
Serum thromboxane B2 (TxB2) serum concentration - Area under the effect curve (AUEC) of the % Change from baseline (CFB) in serum TxB2 concentration (TxB2 suppression)
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The goal of this clinical trial is to compare the pharmacodynamics (PD), pharmacokinetics (PK), safety, and tolerability of acetylsalicylic acid powder for oral inhalation (i-ASA) with non-enteric-coated chewable aspirin (C-ASA) in healthy adults by demonstrating bioequivalence.

In the first treatment period, subjects will be randomized to receive either a single dose (100 mg) of I-ASA powder via a Dry Powder Inhaler (DPI) OR a single dose (162 mg) of C-ASA tablets. After a washout period, subjects will be crossed over to receive the other treatment in the second treatment period. All subjects will receive both treatments during the study. Each single dose treatment will be followed by up to 24 hours of serial post-dose PK, PD, and safety/tolerability assessments.

Registry
clinicaltrials.gov
Start Date
October 14, 2022
End Date
March 9, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Vectura, Inc.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female, ≥18 and ≤55 years of age, with BMI \>18.5 and \<32.0 kg/m2 and body weight ≥50.0 kg for males and ≥45.0 kg for females.
  • Healthy as defined by:
  • the absence of clinically significant illness and surgery within 4 weeks prior to dosing.
  • the absence of clinically significant history of neurological, endocrine, cardiovascular, pulmonary, respiratory, hematological (e.g., thrombocytopenia, neutropenia, bleeding disorders), immunological, psychiatric, gastrointestinal, renal, hepatic, and metabolic disease.
  • Female subjects of non-childbearing potential must be:
  • post-menopausal OR
  • surgically sterile at least 3 months prior to dosing.
  • Sexually active female subjects of childbearing potential must be willing to use an acceptable contraceptive method throughout the study as defined in the protocol.
  • Current non-smoker: no use of tobacco or nicotine products, including any smoking cessation nicotine-containing products (i.e., nicotine replacement therapy \[patch, spray, inhaler, gum, lozenge, bupropion SR, clonidine and nortriptyline\], e-cigarettes, etc.) for at least 3 months prior to screening.
  • Agrees to refrain from alcohol consumption for at least 48 hours prior to admission and 48 hours after drug administration of each period.

Exclusion Criteria

  • Any clinically significant abnormal finding at physical examination at screening.
  • Positive serology test results for HBsAg, HCV antibody, or HIV antigen and antibody, at screening.
  • Positive pregnancy test or lactating female subject.
  • Positive urine drug screen, urine cotinine test, or alcohol breath test.
  • Known allergic reactions, hypersensitivity or contraindications to aspirin (ASA), ibuprofen, other NSAIDs, or other related drugs, or to any excipient in the formulation.
  • Known lack of response (lack of effect) to aspirin in the past.
  • Clinically significant x-ray, ECG abnormalities or vital signs abnormalities at screening.
  • Clinically significant abnormal laboratory parameters including:
  • Hematocrit value ≤ 32%;
  • Platelet count \<142,000 or \> 450,000 platelets per µL;

Arms & Interventions

Arm 1: I-ASA 100mg, then C-ASA 162mg tablet

Treatment A: Single dose of 100 mg ASA powder for oral inhalation (I-ASA) via DPI. Treatment B: Single dose of 162 mg chewable non-enteric-coated Aspirin (C-ASA).

Intervention: ASA

Arm 1: I-ASA 100mg, then C-ASA 162mg tablet

Treatment A: Single dose of 100 mg ASA powder for oral inhalation (I-ASA) via DPI. Treatment B: Single dose of 162 mg chewable non-enteric-coated Aspirin (C-ASA).

Intervention: non-enteric-coated chewable aspirin

Arm 2: C-ASA 162mg tablet, then I-ASA 100mg

Treatment B: Single dose of 162 mg chewable non-enteric-coated Aspirin (C-ASA). Treatment A: Single dose of 100 mg ASA powder for oral inhalation (I-ASA) via DPI.

Intervention: ASA

Arm 2: C-ASA 162mg tablet, then I-ASA 100mg

Treatment B: Single dose of 162 mg chewable non-enteric-coated Aspirin (C-ASA). Treatment A: Single dose of 100 mg ASA powder for oral inhalation (I-ASA) via DPI.

Intervention: non-enteric-coated chewable aspirin

Outcomes

Primary Outcomes

Serum thromboxane B2 (TxB2) serum concentration - Area under the effect curve (AUEC) of the % Change from baseline (CFB) in serum TxB2 concentration (TxB2 suppression)

Time Frame: 24 hours post-dose

Secondary Outcomes

  • Peak plasma concentrations (Cmax) of ASA(pre-dose. minutes post-dose: 2, 5, 10, 20, 30, 45, 60, 120, 180, 360, 480, 720 and 1440)
  • Area under the plasma concentration versus time curve (AUC0-t)(pre-dose. minutes post-dose: 2, 5, 10, 20, 30, 45, 60, 120, 180, 360, 480, 720 and 1440)
  • Time to peak plasma concentrations (Tmax) of ASA(pre-dose. minutes post-dose: 2, 5, 10, 20, 30, 45, 60, 120, 180, 360, 480, 720 and 1440)
  • Time to peak plasma concentrations (Tmax) of SA(pre-dose. minutes post-dose: 2, 5, 10, 20, 30, 45, 60, 120, 180, 360, 480, 720 and 1440)
  • Incidence and frequency of Adverse Events.(screening through the 7-day to follow-up period)
  • TxB2 serum concentration - AUEC of the % CFB in serum TxB2 concentration (TxB2 suppression)(30 minutes post-dose)
  • Time to significant inhibition of platelet aggregation (<550 ARU).(assessed up to 24 hours post-dose)
  • Peak plasma concentrations (Cmax) of SA(pre-dose. minutes post-dose: 2, 5, 10, 20, 30, 45, 60, 120, 180, 360, 480, 720 and 1440)
  • Area under the plasma concentration versus time curve (AUC0-inf)(pre-dose. minutes post-dose: 2, 5, 10, 20, 30, 45, 60, 120, 180, 360, 480, 720 and 1440)
  • Proportion of subjects achieving significant inhibition of platelet aggregation (<550 Aspirin Reaction Units [ARU])(2 minutes post-dose)

Study Sites (2)

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