55 Participants NeededMy employer runs this trial

ABS-1230 for Epilepsy

(KYRON Trial)

MD
MD
Overseen ByMedical Director Actio Biosciences, Inc.
Age: < 65
Sex: Any
Trial Phase: Phase 2
Sponsor: Actio Biosciences, Inc.
Must be taking: Antiseizure medications
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment called ABS-1230 to determine its safety and effectiveness for people with KCNT1-related epilepsy, a condition causing frequent motor seizures. Participants will receive either ABS-1230 or a placebo (a substance with no active treatment) to compare effects. It is suitable for individuals diagnosed with KCNT1-related epilepsy who experience at least four motor seizures per week. Participants should not take certain medications and must maintain stable epilepsy medications during the trial.

As a Phase 2 trial, this research focuses on measuring the treatment's effectiveness in an initial, smaller group, offering a chance to contribute to important advancements in epilepsy care.

Will I have to stop taking my current medications?

You can continue taking your current antiseizure medications as long as you are not taking more than six and can keep the doses stable. However, you cannot take phenytoin, carbamazepine, stiripentol, or quinidine.

Is there any evidence suggesting that ABS-1230 is likely to be safe for humans?

Research has shown that ABS-1230 has undergone safety testing in healthy volunteers. In these past studies, participants tolerated all doses well, experiencing no serious side effects. This finding reassures those considering joining the trial, as it indicates the treatment has been relatively safe in early testing.

The medicine specifically targets the genetic changes causing seizures in people with KCNT1-related epilepsy, making ABS-1230 a promising option for addressing the root cause of the problem.

While the current trial will provide more detailed information, previous safety findings suggest ABS-1230 could be a safe choice for participants.12345

Why do researchers think this study treatment might be promising for epilepsy?

Unlike standard epilepsy treatments like antiepileptic drugs, which often work by stabilizing electrical activity in the brain, ABS-1230 is unique because it targets a novel pathway that may more effectively control seizures. Researchers are excited about ABS-1230 due to its potential to provide relief for patients who do not respond well to existing medications. Additionally, the different parts of the study, including the placebo comparison, highlight its distinctiveness in terms of understanding its effectiveness and safety comprehensively.

What evidence suggests that ABS-1230 might be an effective treatment for epilepsy?

Research has shown that ABS-1230 might help treat KCNT1-related epilepsy. Early studies in mice found that this treatment can greatly reduce seizures by targeting changes in the KCNT1 gene. The results suggest that higher doses of ABS-1230 lead to fewer seizures. This treatment is specifically designed to help people with this type of epilepsy. Although information from human studies remains limited, these early results are promising. Participants in this trial will receive ABS-1230 at different stages to evaluate its effectiveness and safety.12567

Are You a Good Fit for This Trial?

This trial is for children and young adults (1 month to under 22 years old) diagnosed with KCNT1-related epilepsy who have at least 4 motor seizures per week. Participants must be on no more than 6 seizure medications, with stable doses during the study.

Inclusion Criteria

I take 6 or fewer seizure medications and can keep my doses stable.
I have epilepsy caused by a KCNT1 gene mutation, confirmed by my doctor.
I am between 1 month and 22 years old.
See 1 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment Part 1

Participants receive ABS-1230 for 12 weeks

12 weeks

Follow-up Part 1

Participants are monitored for safety and effectiveness after treatment

2 weeks

Treatment Part 2

Participants receive ABS-1230 or placebo for 12 weeks

12 weeks

Follow-up Part 2

Participants are monitored for safety and effectiveness after treatment

2 weeks

Open-label Extension

Participants may opt into continuation of treatment long-term with ABS-1230

Up to 1 year

What Are the Treatments Tested in This Trial?

Interventions

  • ABS-1230

Trial Overview

The study compares a new drug called ABS-1230 to a placebo in young people with KCNT1-related epilepsy. It looks at safety, how well the body handles the drug, and its effects on seizures.

How Is the Trial Designed?

4

Treatment groups

Experimental Treatment

Group I: Placebo (Part 2)Experimental Treatment1 Intervention
Group II: ABS-1230 (Part 3)Experimental Treatment1 Intervention
Group III: ABS-1230 (Part 2)Experimental Treatment1 Intervention
Group IV: ABS-1230 (Part 1)Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Actio Biosciences, Inc.

Lead Sponsor

Citations

Actio Biosciences Announces Preclinical Data Highlighting ...

The preclinical data support the therapeutic potential of ABS-1230 to reduce seizures by selectively inhibiting mutations of the KCNT1 gene, ...

NCT07600736 | A Study to Investigate the Safety, ...

Study Overview. Brief Summary. This trial will evaluate the safety, tolerability, pharmacokinetics, and clinical activity of ABS-1230 compared ...

Actio doses first subject in trial of ABS-1230 for epilepsy

Preclinical trials have demonstrated that ABS-1230 inhibits all pathogenic mutations tested in the KCNT1 gene, suggesting its potential as a ...

ABS-1230 enters phase 1b/2 testing in KCNT1-related ...

No efficacy results from the patient trial are available. The only clinical safety data disclosed in the release come from a phase 1a healthy ...

Actio Biosciences to Present New Preclinical Data for ABS ...

Actio is also conducting preclinical studies to evaluate the therapeutic potential of ABS-1230 in more prevalent genetic epilepsies with related ...

A Study to Investigate the Safety, Tolerability ...

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

Actio Biosciences begins trial of ABS-1230 for epilepsy

The ongoing KYRON Phase Ib/II study will examine the tolerability, pharmacokinetics, and safety of ABS-1230. Salong Debbarma May 11, 2026.