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JNJ-40411813

Alternative Names: jnj-40411813, jnj40411813, jnj 40411813, ADX71149, ADX-71149, ADX 71149
Clinical Status: Active
Latest Update: 2025-04-25
Latest Update Note: News Article

Product Description

JNJ-40411813 is a positive allosteric modulator of mGluR2 for the treatment of seizures being developed by Addex and Johnson & Johnson. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/25735992/)

Mechanisms of Action: MGLUR2/3 Modulator

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Johnson & Johnson
Company Location: NEW BRUNSWICK NJ 08933
Company CEO: Joaquin Duato
Additional Commercial Interests: Addex Pharma

Clinical Description

Map of Global Clinical Trials for JNJ-40411813

Countries in Clinic: Belgium, Germany, Japan, Korea, Poland, Russia, Spain, Ukraine, United States

Active Clinical Trial Count: 3

Recent & Upcoming Milestones

  • Clinical Outcomes Reported - Addex presented P2 Epilepsy results on 2024-04-29 for JNJ-40411813
  • Clinical Outcomes Reported - Addex announced they will present P2 Epilepsy results in 2Q24 for JNJ-40411813

Highest Development Phases

Phase 2: Seizures

Phase 1: Epilepsy

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

jRCT2071200090

P1

Active, not recruiting

Epilepsy

2021-05-25

CR108943

P2

Completed

Seizures

2024-02-08

50%

2024-03-13

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

A study to investigate JNJ-40411813 in combination with levetiracetam in epilepsy

P2

Completed

Seizures

2024-02-08

50%

2025-05-27

Treatments