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esketamine

Generic: ESKETAMINE HYDROCHLORIDE·Brand: SPRAVATO, Spravato

esketamine: 3 clinical trials tracked.

esketamine evidence translation

What we can confirm

3 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about esketamine, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence0 indications · 2 study sponsors

Related indications

No linked indication is available.

Clinical Trials (3)

A Randomized, Double-blind, Multicenter, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Esketamine Nasal Spray, Administered as Monotherapy, in Adult Participants With Treatment-resistant Depression

NCT07716098·Phase 3·GHRS
Recruiting

Primary endpoint: Double-Blind (DB) Treatment Phase: Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) Total Score From Day 1 to the End of the 4-Week Double-Blind Treatment Phase

InterventionalRandomizeddouble348 targetStarted 2026-07Completion 2029-0915 sites · Japan, Taiwan, United StatesJanssen Research & Development, LLC

Effect of Esketamine on Postoperative Sleep in Postmenopausal Women

Not yet recruiting

Primary endpoint: The incidence of postoperative sleep disturbance (PSD) on postoperative day 1.

InterventionalRandomizedtriple164 targetStarted 2026-03Completion 2026-122 sites · ChinaZhuan Zhang

A Double-blind, Randomized, Psychoactive Placebo-controlled Study to Evaluate the Efficacy and Safety of Intranasal Esketamine 84 mg in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder in Adolescent Participants With Acute Suicidal Ideation or Behavior

NCT07227454·Phase 3·GHRS
Recruiting

Primary endpoint: Change from Baseline in Depressive Symptoms Measured by Children's Depression Rating Scale - Revised (CDRS-R) Total Score at 24 Hours Post First Dose

InterventionalRandomizeddouble258 targetStarted 2026-01Completion 2031-0935 sites · Brazil, Hungary, Italy, Romania…Janssen Research & Development, LLC