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Ketamine plus usual care

The University of Texas Health Science Center, Houston · FDA-approved active Small molecule Quality 5/100

Ketamine blocks NMDA glutamate receptors in the brain, producing rapid-onset dissociative anesthesia and analgesic effects.

Ketamine plus usual care, marketed by The University of Texas Health Science Center, Houston, is a treatment currently available in the market. A key strength is the protection provided by the key composition patent, which expires in 2028. The primary risk is the lack of detailed revenue data and key trial results, which may limit strategic planning and investor confidence.

At a glance

Generic nameKetamine plus usual care
SponsorThe University of Texas Health Science Center, Houston
Drug classNMDA receptor antagonist
TargetNMDA receptor
ModalitySmall molecule
Therapeutic areaAnesthesia, Pain Management
PhaseFDA-approved

Mechanism of action

Ketamine is a non-competitive antagonist at the N-methyl-D-aspartate (NMDA) receptor, a subtype of glutamate receptor. This blockade interrupts pain signal transmission and produces dissociative anesthesia. When combined with usual care, ketamine may provide enhanced analgesia and sedation in acute or perioperative settings.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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