Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
MDMA + citalopram is a combination therapy under development for the treatment of post-traumatic stress disorder (PTSD). It consists of 3,4-methylenedioxymethamphetamine (MDMA), an entactogen and monoamine releasing agent, and citalopram, a selective serotonin reuptake inhibitor (SSRI). In this regimen, MDMA is administered first to produce its psychoactive effects. Citalopram is given several hours later to reduce negative after-effects such as mood disturbances ("Blue Mondays") and to mitigate MDMA-induced serotonergic neurotoxicity. The mechanism involves MDMA increasing synaptic serotonin by promoting its release via the serotonin transporter, while delayed administration of citalopram inhibits further serotonin reuptake and blocks neurotoxic effects without significantly diminishing the desired acute effects of MDMA. This approach aims to preserve therapeutic benefits while reducing adverse outcomes[1][2][3].
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 MDMA + citalopram.