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NCT07600736RecruitingPhase 2

A Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Clinical Activity of ABS-1230 in Pediatric and Young Adult Participants With KCNT1-related Epilepsy

A Phase 1b/2 Study to Assess the Safety, Tolerability, Pharmacokinetics, and Clinical Activity of ABS-1230 Administered to Pediatric and Young Adult Participants With KCNT1-Related Epilepsy

Source: ClinicalTrials.gov · Last updated 15 Oct 2026

Brief summary (registry, in English)

This trial will evaluate the safety, tolerability, pharmacokinetics, and clinical activity of ABS-1230 compared with placebo in participants with KCNT1-related epilepsy

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
61 (estimated)
First submitted
14 May 2026
Start date
18 May 2026
Primary completion date
31 Jan 2027
Lead sponsor
Actio Biosciences, Inc.
Diseases
Epilepsy
NCT number
NCT07600736

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 61
  • From 18 May 2026 to the primary completion date, 31 Jan 2027
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Is currently taking phenytoin, carbamazepine, stiripentol, or quinidine

Other illness

  • Has a medical condition that, in the opinion of the investigator, would limit the participant's ability to participate in the study or might compromise participant safety or interfere with evaluation of the study drug.

Who the study is looking for

  • Aged 1 month to \<22 years
  • Clinician-confirmed diagnosis of KCNT1-related epilepsy
  • Has an average of at least 4 countable motor seizures per week
  • Is taking no more than 6 antiseizure medications (ASM) and is able to keep stable doses of ASMs for the duration of Part 1 or Part 2

Age in the registry: 1 month to 21 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Northeast Regional Epilepsy Group
Coordinator of this site? Confirm its status
HackensackUnited StatesRecruiting
University of Rochester Medical Center
Coordinator of this site? Confirm its status
RochesterUnited StatesNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.