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Completed

NCT Number: NCT05005520

Study of DTRI-031 in Healthy Volunteers

A randomized, double-blind, single center, placebo-controlled phase 1 study in healthy volunteers to assess safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of a single intravenous (iv) injection of DTRI-031

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Nucleus Network

Melbourne, Victoria, 3004, Australia

About this study

Up to 5 cohorts of 8 healthy volunteers for a total of 40 volunteers will be randomized to either DTRI-031 or matching placebo (6 active:2 placebo). Two sentinel subjects, one randomized to each group, will be dosed at least 1 day prior to dosing of the remaining subjects in a cohort.

Subjects will complete a screening visit up to 28 days prior to administration of study drug to confirm eligibility. Eligible subjects will arrive at the phase 1 unit up to 24 hours prior to Day 1 and remain until completion of 24-hour assessments. Subjects will return for a Day 7 follow-up visit and receive a safety assessment telephone call on Day 28.

A Safety Review Committee will review individual subject and aggregate group safety data following each dose-based study cohort and recommend whether the trial should continue to the next cohort.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18-55 years of age
  • Ability to provide written consent
  • Weight 50-110 kg with BMI 18.5-32 kg/m2
  • Willingness to use contraceptives
  • Negative COVID-19 test
  • Negative results for alcohol and drugs of abuse

Exclusion criteria

  • Pregnant or lactating females
  • Familial bleeding disorder or individual or family history of bleeding diathesis or coagulopathy
  • Females with active menstruation on day of dosing
  • Use of prescription medications known to affect platelet function
  • Use of NSAIDs, aspirin, anti-platelet or anti-coagulation therapy within 10 days of dosing
  • Contraindication to anticoagulation or increased bleeding risks
  • History of thrombocytosis, high platelet count, intracranial bleeding, aneurysm, stroke, vascular disease
  • History of peptic ulcer disease, gastrointestinal or genitourinary bleed, severe trauma, fracture, major surgery of biopsy of parenchymal organ within past 3 months
  • Planned surgery during the study
  • Any clinical significant abnormality at screening
  • Use of investigational drug in past 30 days or 5 half lives
  • Concurrent enrollment in another clinical study or more than 3 clinical studies in past 12 months
  • Any prior history of substance abuse or treatment or positive urine screen for drugs of abuse or positive breathalyzer test

Treatment and study plan

DTRI-031

Drug

Investigational drug

Placebo

Drug

Matching placebo to DTRI-031

Primary outcomes

  1. Safety as assessed by adverse events (AEs)

    Time frame: From dosing (DTRI-031 or placebo) to final visit (Day 28)

    Incidence of treatment-emergent AEs

Secondary outcomes

  1. Pharmacokinetics as measured by DTRI-031 plasma levels

    Time frame: From dosing to 24 hours after dosing

    Plasma concentration of DTRI-031 (after single dose of drug)

  2. Plasma von Willebrand Factor (vWF) levels

    Time frame: From dosing to 24 hours after dosing

    Level of vWF following single administration of drug

  3. Platelet Function

    Time frame: From dosing to 24 hours after dosing

    Whole blood platelet function closure times

Sponsors and collaborators

Lead sponsor

Basking Biosciences, Inc.

Industry

Registry information

Official study title

A Randomized, Double-Blind, Single-Center, Placebo-Controlled Phase 1 Study to Evaluate the Safety, Tolerability, PK and PD of Intravenous DTRI-031 in Healthy Volunteers

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Aug 13, 2021
Registry last updated
Jul 19, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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