Ireland
--:--IST
Recruiting Phase 3

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

NCT07224581 · tracked via the Priya Life Science Germany tracker
Phase
Phase 3
Started
2026-01-05
Last updated
2026-11-12

Condition(s) studied

GRIN-related Neurodevelopmental Disorder

Investigational drug(s) / intervention(s)

Radiprodil →Placebo

Radiprodil: Radiprodil oral suspension

Placebo: Placebo-to-match radiprodil oral suspension

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

Sex
ALL
Min age
1 Month
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: Part A, Participant: * Diagnosed with GRIN-NDD with GRIN1, GRIN2A, GRIN2B, or GRIN2D gene variants known to result in GoF of the NMDA receptor * Phase 3 Cohort 1 (Qualifying Seizures Cohort) ONLY: Experiencing at least 1 CMS per week 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: With significant 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 should remain on stable doses throughout study participation * On stable nonpharmacological treatments such as ketogenic diet and should remain stable 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 Criteria: PART A, 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 or study drug administration or the conduct 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.

Primary outcome measure(s)

  • Part A - Phase 3 Cohort 1 (Qualifying Seizures Cohort): Countable motor seizures (CMS) — 12 weeks
  • Part A - Phase 3 Cohort 2 (Without Qualifying Seizures Auxiliary Cohort): Adverse events (AEs), serious adverse events (SAEs), and adverse drug reactions (ADRs) — 24 weeks
  • Part B - Open-Label Extension: Adverse events (AEs), serious adverse events (SAEs), and adverse drug reactions (ADRs) — Average of 2 years

Trial sites (62)

FacilityCityRegionStatus
UCLA Health - Ronald Reagan UCLA Medical Center Los Angeles California Recruiting
Lucile Packard Children's Hospital Palo Alto California Recruiting
Children's Hospital Colorado - Anschutz Medical Campus Aurora Colorado Recruiting
Children's National Hospital Washington D.C. District of Columbia Recruiting
Children's National Medical Center Washington D.C. District of Columbia Recruiting
Nicklaus Children's Hospital Miami Florida Recruiting
Pediatric Neurology and Epilepsy Winter Park Florida Recruiting
Iowa Health Care - Pediatric Neurology & Specialty Clinic Iowa City Iowa Recruiting
Boston Children's Hospital Boston Massachusetts Recruiting
Northeast Regional Epilepsy Group (NEREG) - Hackensack Hackensack New Jersey Recruiting
Columbia University - Harkness New York New York Recruiting
Duke Health-Duke Children's Hospital & Health Center Durham North Carolina Recruiting
Duke University Health System Durham North Carolina Recruiting
Cincinnati Children's Hospital Medical Center Cincinnati Ohio Not Yet Recruiting
Cincinnati Children's Hospital Medical Center Cincinnati Ohio Recruiting
Children's Hospital of Philadelphia Philadelphia Pennsylvania Recruiting
Child Neurology Consultants of Austin - South Austin Austin Texas Recruiting
Children's Health Specialty Center, Dallas Dallas Texas Recruiting
The University of Texas Southwestern Medical Center (UTSW) Dallas Texas Recruiting
UTHealth Houston Houston Texas Recruiting
Seattle Children's Hospital Seattle Washington Recruiting
Queensland Children's Hospital South Brisbane Queensland Recruiting
Austin Health Heidelberg Victoria Recruiting
UZ Brussel Brussels Belgium Recruiting
University Hospital Antwerp Edegem Belgium Recruiting
Centre Hospitalier Universitaire d'Angers (CHU Angers) Angers France Recruiting
CHU Angers Angers France Recruiting
Hospices Civils de Lyon Bron France Recruiting
Hospices Civils De Lyon Bron France Recruiting
CHU de Dijon Dijon France Recruiting
AP HM Hopital d'enfants de la Timone Marseille France Recruiting
Hopital Necker Enfants Malades (APHP) Paris France Recruiting
Hôpital Necker Enfants Malades Paris France Recruiting
Hopital des Enfants ; CHU Toulouse Toulouse France Recruiting
CHU Toulouse - Hôpital Purpan Toulouse France Recruiting
Universitatsklinikum Leipzig Leipzig Saxony Recruiting
Universitatsklinikum OWL der Universitat Bielefeld Bielefeld Germany Recruiting
Universitatsmedizin Greifswald Klinik und Poliklinik fur Frauenheilkunde und Geburtshilfe Greifswald Germany Recruiting
Klinik und Policlinik fur Kinder - und Jugendmedizin Leipzig Germany Recruiting
Azienda Ospedaliera Universitaria Meyer IRCCS Florence Viale Pieraccini Recruiting

+ 22 more sites — see the full list on the official registry below.

More GRIN Therapeutics, Inc. trials in Germany

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 NCT07224581 on ClinicalTrials.gov ↗ ← All trials in Germany