Available Technologies

Novel Therapeutics for Obsessive-Compulsive Disorder and Process Addictions

Therapeutic candidates showing strong efficacy and rapid onset in treating treatment-resistant psychiatric disorders, such as OCD and process addictions

Background

OCD and process addictions are characterized by repetitive behaviors that are difficult for patients to voluntarily control, significantly impairing daily functioning.
Common pharmacological treatments for OCD include high-dose, long-term administration of antidepressants such as selective serotonin reuptake inhibitors (SSRIs). However, over half of patients are classified as treatment-resistant, showing little or no response to antidepressants.
Moreover, process addictions - such as gaming disorder and internet addiction - are newly recognized behavioral conditions, and currently, no approved pharmacological treatments are available.

Description and Advantages

Leveraging proprietary analyses of large-scale medical datasets, researchers at Kyoto University developed a drug-induced mouse model of OCD that is unresponsive to SSRIs, effectively mimicking treatment-resistant OCD. In-depth analysis of the model revealed an imbalance between D1-and D2-receptor-positive neurons in the striatum leading to the identification of a key target gene and a promising therapeutic candidate capable of restoring this balance (Fig. 1).

Offers hope for majority of OCD patients resistant to SSRIs
Shared neural mechanisms in OCD and process addictions suggest newtherapeutic potential

スクリーンショット 2025-06-23 140430.png

Figure1.EffectofthecandidatedrugonRepetitiveBehaviorinanOCDMouseModel
Toevaluatethedrug'sefficacyinreducingrepetitivebehaviors,arodentmodelofcompulsivebehavior-specifically,therepeatedgnawingofbeddingmaterial-wasusedasanindexofOCD-likesymptoms.OCDmodelmicewereintraperitoneallyadministeredeitherthenewdrugcandidate,anexistingantidepressant(citalopram),ananxiolytic(diazepam),orvehiclecontroloncedaily.Stereotypicbehaviorwasobservedfor10minutesondays1and4oftreatment.Administrationofthenewdrugcandidateat3mg/kgsignificantlysuppressedstereotypicbehavior(left),whereasneithertheexistingantidepressantnortheanxiolyticshowedsignificanteffects(right).

Development
Status
•Validated efficacy of candidate drug in OCD model mice
•Ongoing evaluation for potential indication expansion
Offer •Patent License
•Collaborative Research
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