Beeline: A Phase 3 Study in GRIN-related Neurodevelopmental Disorder

Last updated: February 25, 2026
Sponsor: GRIN Therapeutics, Inc.
Overall Status: Active - Recruiting

Phase

3

Condition

N/A

Treatment

Placebo

Radiprodil

Clinical Study ID

NCT07224581
Beeline RAD-GRIN-101
  • Ages 1-18
  • All Genders

Study Summary

The Phase 3 portion of Study RAD-GRIN-101 is a multinational, multicenter, randomized, double-blind, placebo-controlled trial followed by an open-label extension to evaluate the efficacy and safety of radiprodil in participants with GRIN-related neurodevelopmental disorder (GRIN-NDD) with a gain-of-function (GoF) genetic variant.

This study will enroll two cohorts: one cohort of participants with a minimal number of countable motor seizures (with or without behavioral symptoms) (Phase 3 Cohort 1: Qualifying Seizures Cohort); and a second cohort with disease symptoms but no seizures or fewer seizures than required for the Qualifying Seizures Cohort (Phase 3 Cohort 2: Without Qualifying Seizures Auxiliary Cohort).

Participants in each cohort will be randomized 1:1 to receive active drug (radiprodil) or matching placebo (Part A). Following completion of Part A, all eligible participants (including those previously on placebo) may continue into the open-label extension period (Part B) to receive radiprodil.

The placebo-controlled portion is expected to be approximately 16 weeks for participants in Phase 3 Cohort 1 and 28 weeks for participants in Phase 3 Cohort 2.

The study will evaluate the effect of radiprodil on seizures and non-seizure symptoms and assess safety.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Part A, Participant:

  • Diagnosed with GRIN-NDD with GRIN1, GRIN2A, GRIN2B, or GRIN2D gene variants known toresult in GoF of the NMDA receptor

  • Phase 3 Cohort 1 (Qualifying Seizures Cohort) ONLY: Experiencing at least 1 CMS perweek and ≥4 CMS (generalized or focal) during screening

  • With history of inadequate response to at least 2 standard antiseizure medications (ASMs)

  • Phase 3 Cohort 2 (Without Qualifying Seizures Auxiliary Cohort) ONLY: Withsignificant neurodevelopmental symptoms and a GRIN-CGI-S score ≥4

  • On a stable dose of standard ASMs for at least 4 weeks prior to screening and shouldremain on stable doses throughout study participation

  • On stable nonpharmacological treatments such as ketogenic diet and should remainstable throughout study participation

Part B:

  • Participant has completed Part A and is eligible to continue study participation according to the judgement of the investigator and sponsor.

Exclusion

Exclusion Criteria:

PART A, Participant:

  • Has clinically relevant medical, neurologic, or psychiatric condition and/orbehavioral disorder (including those related to GRIN-NDD) that would preclude orjeopardize participant's safe participation or study drug administration or theconduct of the study according to the judgement of the investigator or sponsor.

  • Is receiving >4 standard ASMs at screening

  • Has a body weight of less than 5 kg at screening

Part B:

  • Participant has clinically relevant medical, neurologic, or psychiatric condition and/or behavioral disorder (including those related to GRIN-NDD) that would preclude or jeopardize participant's safe participation of study drug administration or the conduct of the study according to the judgement of the investigator or sponsor.

Study Design

Total Participants: 100
Treatment Group(s): 2
Primary Treatment: Placebo
Phase: 3
Study Start date:
January 05, 2026
Estimated Completion Date:
July 31, 2028

Study Description

Participants are assigned in a 1:1 ratio to receive either radiprodil or placebo during Part A with the opportunity to receive radiprodil in the Open-Label Extension, Part B. The dosing regimen includes a fixed titration schedule over 4 weeks.

This study is divided into the following parts:

Part A: Randomized, double-blind, placebo-controlled

  • Screening/Observation Period: To assess eligibility

  • Titration Period (approximately 4 weeks): Titration of radiprodil or placebo to target dose

  • Maintenance Period (Part A): Target dose of radiprodil or placebo maintained for 12 weeks (Phase 3 Cohort 1) or 24 weeks (Phase 3 Cohort 2)

  • Tapering and Follow-up Period: Gradual decrease and Follow-up Period for participants not entering Part B

Part B: Open-label safety follow-up period

  • Open-Label Treatment Period: Participants will continue to receive radiprodil until such time as either the participant withdraws/is withdrawn from the study, sponsor terminates the study, or market access is available

  • Tapering and Follow-up Period: Gradual decrease and follow-up observation period for participants upon leaving the study

Connect with a study center

  • UCLA Clinical & Translational Research Center

    Los Angeles 5368361, California 5332921 90095
    United States

    Active - Recruiting

  • UCLA Health-Ronald Reagan Medical Center

    Los Angeles 5368361, California 5332921 90095
    United States

    Site Not Available

  • Lucile Packard Children's Hospital

    Palo Alto 5380748, California 5332921 94304
    United States

    Active - Recruiting

  • Children's Hospital Colorado - Anschutz Medical Campus

    Aurora 5412347, Colorado 5417618 80045
    United States

    Active - Recruiting

  • Children's National Hospital

    Washington D.C. 4140963, District of Columbia 4138106 20010
    United States

    Active - Recruiting

  • Nicklaus Children's Hospital

    Miami 4164138, Florida 4155751 33155
    United States

    Active - Recruiting

  • Pediatric Neurology and Epilepsy

    Winter Park 4178560, Florida 4155751 32789
    United States

    Active - Recruiting

  • Ann & Robert H Lurie Children's Hospital of Chicago

    Chicago 4887398, Illinois 4896861 60611
    United States

    Site Not Available

  • Iowa Health Care - Pediatric Neurology & Specialty Clinic

    Iowa City 4862034, Iowa 4862182 52242
    United States

    Active - Recruiting

  • University of Iowa Hospitals & Clinics

    Iowa City 4862034, Iowa 4862182 52242
    United States

    Site Not Available

  • Mid-Atlantic Epilepsy and Sleep Center

    Bethesda 4348599, Maryland 4361885 20817
    United States

    Site Not Available

  • Boston Children's Hospital

    Boston 4930956, Massachusetts 6254926 02115
    United States

    Active - Recruiting

  • Northeast Regional Epilepsy Group (NEREG) - Hackensack

    Hackensack 5098706, New Jersey 5101760 07601
    United States

    Active - Recruiting

  • Columbia University - Harkness

    New York 5128581, New York 5128638 10032
    United States

    Active - Recruiting

  • Duke Health-Duke Children's Hospital & Health Center

    Durham 4464368, North Carolina 4482348 27705
    United States

    Active - Recruiting

  • Cincinnati Children's Hospital Medical Center

    Cincinnati 4508722, Ohio 5165418 45229
    United States

    Site Not Available

  • Children's Hospital of Philadelphia

    Philadelphia 4560349, Pennsylvania 6254927 19104
    United States

    Active - Recruiting

  • Child Neurology Consultants of Austin - South Austin

    Austin 4671654, Texas 4736286 78757
    United States

    Active - Recruiting

  • The University of Texas Southwestern Medical Center (UTSW)

    Dallas 4684888, Texas 4736286 75390
    United States

    Site Not Available

  • UTHealth Houston

    Houston 4699066, Texas 4736286 77030
    United States

    Active - Recruiting

  • Seattle Children's Hospital

    Seattle 5809844, Washington 5815135 98105
    United States

    Active - Recruiting

  • Froedtert & Medical College of Wisconsin

    Milwaukee 5263045, Wisconsin 5279468 53226
    United States

    Site Not Available

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