Drug intelligence / Profile preview

clomipramine + diazepam

Development stage
Unknown
Lead developer
Novartis
Modality
Small Molecules
Administration
Oral, Intramuscular, Intravenous, Rectal
01

Overview

Clomipramine + diazepam is a combination of two pharmaceutical drugs, each with distinct mechanisms of action. Clomipramine is a tricyclic antidepressant (TCA) primarily used for the treatment of obsessive-compulsive disorder and other conditions with an obsessive-compulsive component, such as depression and certain anxiety disorders. It acts mainly by inhibiting the reuptake of serotonin and norepinephrine in the central nervous system, increasing their synaptic concentrations. Diazepam is a benzodiazepine indicated for symptomatic management of anxiety, muscle spasms, acute alcohol withdrawal, and as an adjunct in certain types of epilepsy. It works by enhancing the effect of gamma-aminobutyric acid (GABA) at the GABA-A receptor complex, producing anxiolytic, anticonvulsant, sedative-muscle relaxant effects. The combination may be considered in clinical practice for patients with comorbid anxiety and depressive or obsessive symptoms; however, concurrent use increases risks such as sedation, dizziness, confusion—especially in elderly patients—and should only be undertaken under close medical supervision due to potential drug interactions[2][7]. There are no widely recognized fixed-dose combination products containing both agents; use together typically involves co-prescription rather than a single branded product.

02

Targets

M1 (Muscarinic acetylcholine receptor M1)HRH1 (Histamine H1 Receptor)SERT (Sodium-dependent serotonin transporter)NET (Norepinephrine Transporter)GABRR (GABA-A receptor subunit rho)ADRA1A (α1A)

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