Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Placebo + ketamine refers to a specific pharmacological intervention arm used in clinical research, notably in a Phase 1 pilot study conducted at Yale University (NCT00106119). This combination serves as a control or baseline model for schizophrenia-like symptoms in healthy volunteers. The protocol involves the oral administration of an inactive placebo followed by an intravenous infusion of ketamine. Ketamine acts as a non-competitive antagonist of the N-methyl-D-aspartate (NMDA) receptor, which induces transient cognitive deficits, perceptual alterations, and psychotic symptoms that mimic the pathophysiology of schizophrenia. This model is utilized to evaluate the potential of novel antipsychotic agents, such as glycine transporter-1 (GlyT1) inhibitors, to attenuate these induced symptoms compared to the placebo + ketamine baseline.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on placebo + ketamine.