← Eichor
Study identifier: NCT07156201 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of ABS-1230 Given Orally Compared With Placebo in Healthy Participants Aged 18 to 55 Years

Condition: KCNT1-Related Epilepsy  ·  Sponsor: Actio Biosciences, Inc.

PhasePhase 1
Planned participants74
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersYes

About this study

This first in human trial will evaluate the safety, tolerability, and pharmacokinetics of single ascending doses, multiple ascending doses, and fed and fasted doses of ABS-1230 given orally compared with placebo in adult healthy participants.

This description comes directly from the study's public registry record.

Talk to the study team

Actio Biosciences, Inc.  ·  +1 (858) 679-5891  ·  info@actiobiosciences.com

Always discuss trial participation with your own doctor first.

Locations (1)

Scientia Clinical ResearchSydney, New South Wales, AustraliaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07156201