Ireland
--:--IST
Active, not recruiting Phase 1

Healthy Volunteer Study

NCT07270783 · tracked via the Priya Life Science USA tracker
Phase
Phase 1
Started
2025-12-04
Last updated
2026-10-13

Condition(s) studied

Healthy Volunteer

Investigational drug(s) / intervention(s)

D-2570 →Placebo

D-2570: D-2570

Placebo: Placebo

Study summary

Double Blinded Healthy Volunteer study evaluating D-2570 against placebo in various doses.

Eligibility

Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy volunteer subjects meeting eligibility criteria Exclusion Criteria: * Subjects with ongoing or history of disease or co-morbidities as assessed by Principal Investigator which would make them ineligible for the study * Subjects with a history of drug and alcohol abuse * Subjects taking medications, over the counter or herbal remedies

Primary outcome measure(s)

  • Incidence of adverse events — From Informed Consent through study completion, an average of 48 days
    Incidence of adverse events
  • Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
    Tmax
  • Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
    Cmax
  • Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
    t1/2
  • Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
    MRT
  • Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days.
    AUC0-∞
  • Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
    AUC0-t
  • Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
    CL/F
  • Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
    Vz/F

Trial sites (1)

FacilityCityRegionStatus
Pharmaron Baltimore Maryland

More InventisBio Co., Ltd trials in the USA

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07270783 on ClinicalTrials.gov ↗ ← All trials in the USA