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memantine

Generic: MEMANTINE HYDROCHLORIDE·Brand: MEMANTINE HYDROCHLORIDE, NAMENDA, NAMENDA XR, Namenda, Namzaric

memantine: developed by 4 companies · 7 clinical trials tracked · 5 FDA decisions.

memantine evidence translation

What we can confirm

5 FDA records · 7 tracked trials

What it means

More than one developer is source-backed. Until you choose one, AI stays drug-only and does not guess ownership.

What to watch

Watch active trials and any change in FDA or trial status.
BioSniper AIPage evidence connected

Prepared research question

What is verified about memantine, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 2 study sponsors
Development Pipeline (4)
Clinical Trials (7)

A Randomized Phase 2 Trial of Memory Avoidance Whole Brain Radiotherapy Versus Hippocampal Avoidance Whole Brain Radiotherapy (Athena 2 Trial)

NCT07248228·Phase 2·SUPN
Not yet recruiting

Primary endpoint: Time to neurocognitive failure (NCF)

InterventionalRandomizedopen90 targetStarted 2026-03Completion 2028-111 site · United StatesCase Comprehensive Cancer Center

COMPARATIVE STUDY TO EVALUATE SATISFACTION WITH THE USE OF ORODISPERSIBLE MEMANTINE TABLETS VERSUS CONVENTIONAL TABLETS IN PATIENTS WITH MODERATE TO SEVERE ALZHEIMER'S DISEASE: A PHASE IV, RANDOMIZED, OPEN-LABEL STUDY.

NCT07417670·Phase 4·SUPN
Completed

Primary endpoint: Caregiver treatment satisfaction assessed by the Treatment Satisfaction with Medicines Questionnaire (SATMED-Q)

InterventionalRandomizedopen105 enrolledStarted 2024-10Completion 2025-084 sites · MexicoCarnot Laboratories

A Phase 3 Randomized, Placebo-Controlled Trial Evaluating Memantine for Neurocognitive Protection in Children Undergoing Cranial Radiotherapy as Part of Treatment for Primary Central Nervous System Tumors

NCT04939597·Phase 3
Active, not recruiting

Primary endpoint: The mean slope of the Cogstate composite Z score (an average of detection, Identification, and one-back Z scores, each Z score calculated using Cogstate age-based normative data)

InterventionalRandomizeddouble162 enrolledStarted 2022-05Completion 2027-0950 sites · United StatesChildren's Oncology Group

Memantine Augmentation of Targeted Cognitive Training in Schizophrenia

NCT04857983·Phase 2·SUPN
Completed

Primary endpoint: Positive & Negative Symptom Scale total (PANSSt)

InterventionalRandomizeddouble62 enrolledStarted 2021-07Completion 2025-031 site · United StatesUniversity of California, San Diego

Phase III Trial of Stereotactic Radiosurgery (SRS) Versus Hippocampal-Avoidant Whole Brain Radiotherapy (HA-WBRT) for Brain Metastases From Small Cell Lung Cancer

NCT04804644·Phase 3·CGON
Recruiting

Primary endpoint: Time to neurocognitive failure

InterventionalRandomizedopen200 targetStarted 2021-06Completion 2031-0750 sites · United StatesNRG Oncology

A Randomized Placebo-controlled, Double Blind Phase 2 Clinical Trial of Memantine for the Treatment of Cognitive Impairment in Systemic Lupus Erythematosus

NCT03527472·Phase 2
Completed

Primary endpoint: Repeatable Battery for Assessment of Neuropsychological Status (RBANS) Total Index Score at endpoint (Visit 4)

InterventionalRandomizedquadruple111 enrolledStarted 2018-08Completion 2026-023 sites · United StatesVanderbilt University Medical Center

Memantine for Prevention of Cognitive Late Effects in Pediatric Patients Receiving Cranial Radiation Therapy for Localized Brain Tumors: A Pilot Study

NCT03194906·Phase 2
Completed

Primary endpoint: Percent of Approached Participants Who Consent to Study Participation

InterventionalRandomizedquadruple41 enrolledStarted 2017-11Completion 2023-061 site · United StatesSt. Jude Children's Research Hospital
FDA Decisions5 records
ANDA208237UNKNOWNStandardOralCapsule, Extended Release
Approval1 INDICATIONS AND USAGE Memantine hydrochloride tablets are indicated for the treatment of moderate to severe dementia of the Alzheimer’s type. Memantine hydrochloride tablets are an N-methyl-D-aspartate (NMDA) receptor antagonist indicated for the treatment of moderate to severe dementia of the Alzheimer’s type. (1)(ANIP)FDA ↗
ANDA205365UNKNOWNStandardOralCapsule, Extended Release
Approval1 INDICATIONS AND USAGE Memantine hydrochloride tablets are indicated for the treatment of moderate to severe dementia of the Alzheimer’s type. Memantine hydrochloride tablets are an N-methyl-D-aspartate (NMDA) receptor antagonist indicated for the treatment of moderate to severe dementia of the Alzheimer’s type. (1)(TEVA)FDA ↗
ANDA090052OralTablet
NDA022525Type 3 - New Dosage FormStandardOralCapsule, Extended Release
Approval(RDY)FDA ↗
ANDA090048OralTablet

Frequently asked questions

Who is developing memantine?

memantine is being developed by AbbVie Inc., ANI PHARMACEUTICALS INC, DR REDDYS LABORATORIES LTD and 1 other.

How many clinical trials involve memantine?

BioSniper tracks 7 clinical trials involving memantine.

What is memantine's latest FDA decision?

The most recent tracked FDA decision for memantine is Approval, dated December 15, 2023.