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Clinical Trials/NCT04809818
NCT04809818
Completed
Phase 1

Double-Blind, Randomized, Placebo-Controlled, Phase 1 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Multiple Doses of LT3001 Drug Product and Drug-Drug Interaction in Healthy Adult Subjects

Lumosa Therapeutics Co., Ltd.1 site in 1 country65 target enrollmentMarch 21, 2021

Overview

Phase
Phase 1
Intervention
Apixaban
Conditions
Acute Ischemic Stroke
Sponsor
Lumosa Therapeutics Co., Ltd.
Enrollment
65
Locations
1
Primary Endpoint
Number of Adverse Events
Status
Completed
Last Updated
2 months ago

Overview

Brief Summary

This Phase 1 study is planned to establish the clinical safety and pharmacokinetics profile of multiple dose of LT3001 drug product and to investigate drug interactions of LT3001 with potential concomitant medications in healthy subjects.

Detailed Description

This study is a two-part study. Part A is double-blind, placebo-controlled, and will examine the safety and PK profiles of multiple doses of LT3001 drug product in healthy subjects. Part B is open-label and will assess the safety and PK of LT3001 when coadministered with aspirin, clopidogrel, apixaban or dabigatran.

Registry
clinicaltrials.gov
Start Date
March 21, 2021
End Date
August 5, 2021
Last Updated
2 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subject's body weight is ≥50 kg and BMI is within the range of 18 to 32
  • Subject is a healthy volunteer.
  • Subject's PT, aPTT, and TT are within the normal laboratory range.
  • Subject is a nonsmoker

Exclusion Criteria

  • Subject has a current or recent history of regular alcohol consumption.
  • Subjects who are enrolled in Part B and allergic to acetylsalicylic acid, other salicylates, clopidogrel, thienopyridines (eg, ticlopidine, prasugrel), apixaban or dabigatran.
  • Part B Cohort 2 only: subjects who are poor metabolizers of clopidogrel (CYP2C19\*2/\*2, \*2/\*3, or \*3/\*3 genotype)
  • Subject has a presence or history of coagulation abnormality.
  • Subjects need to receive a surgery or clinical procedures associated with high bleeding risk.
  • Subject has a history of minor bleeding episodes, eg, epistaxis, rectal bleeding, gingival bleeding.
  • Subject has a history of peptic ulcer or gastrointestinal bleeding.

Arms & Interventions

Part B - LT3001 and Apixaban

Multiple doses of LT3001 and Apixaban administered

Intervention: Apixaban

Part A - LT3001 Drug Product

Multiple doses of LT3001 administered by intravenous infusion

Intervention: LT3001 drug product

Part A - Placebo

Multiple doses of Placebo administered by intravenous infusion

Intervention: Placebo

Part B - LT3001 and Aspirin

Multiple doses of LT3001 and Aspirin administered

Intervention: LT3001 drug product

Part B - LT3001 and Aspirin

Multiple doses of LT3001 and Aspirin administered

Intervention: Aspirin

Part B - LT3001 and Clopidogrel

Multiple doses of LT3001 and Clopidogrel administered

Intervention: LT3001 drug product

Part B - LT3001 and Clopidogrel

Multiple doses of LT3001 and Clopidogrel administered

Intervention: Clopidogrel

Part B - LT3001 and Apixaban

Multiple doses of LT3001 and Apixaban administered

Intervention: LT3001 drug product

Part B - LT3001 and Dabigatran

Multiple doses of LT3001 and Dabigatran administered

Intervention: LT3001 drug product

Part B - LT3001 and Dabigatran

Multiple doses of LT3001 and Dabigatran administered

Intervention: Dabigatran

Outcomes

Primary Outcomes

Number of Adverse Events

Time Frame: Adverse events were assessed from baseline through Day 4 post-baseline in Part A, and from baseline through Day 16 post-baseline in Part B.

To evaluate the safety and tolerability of LT3001 administered alone or in combination with aspirin, clopidogrel, apixaban, or dabigatran, as determined by the number and severity of adverse events collected from baseline through Day 4 post-baseline in Part A, and from baseline through Day 16 post-baseline in Part B.

Secondary Outcomes

  • Change From Baseline in Activated Partial Thromboplastin Time (APTT)(16 days)
  • Number of Participants With Prolongation in Platelet Function Test(16 days)
  • Plasma PK Parameters of LT3001 - Cmax(Predose and post-dose time points up to 10 days after dosing)
  • Plasma PK Parameters of LT3001 - Tmax(10 days)
  • Plasma PK Parameters of LT3001 - AUC(10 days)
  • Plasma PK Parameters of Aspirin - Cmax(8 days)
  • Plasma PK Parameters of Aspirin - Tmax(8 days)
  • Plasma PK Parameters of Aspirin - AUC(8 days)
  • Plasma PK Parameters of Clopidogrel - Cmax(10 days)
  • Plasma PK Parameters of Clopidogrel - Tmax(10 days)
  • Plasma PK Parameters of Clopidogrel - AUC(10 days)
  • Plasma PK Parameters of Apixaban - Cmax(8 days)
  • Plasma PK Parameters of Apixaban - Tmax(8 days)
  • Plasma PK Parameters of Apixaban - AUC(8 days)
  • Plasma PK Parameters of Dabigatran - Cmax(8 days)
  • Plasma PK Parameters of Dabigatran - Tmax(8 days)
  • Plasma PK Parameters of Dabigatran - AUC(8 days)

Study Sites (1)

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