Drug intelligence / Profile preview

zicronapine

Development stage
Phase 3
Lead developer
Lundbeck
Modality
Small Molecules
Administration
Oral
01

Overview

Zicronapine (Lu 31-130) is an atypical antipsychotic small molecule that was under development by Lundbeck for the treatment of schizophrenia. It is characterized by a unique pharmacological profile, acting as a potent antagonist at dopamine D1, D2, and serotonin 5-HT2A receptors. Unlike most atypical antipsychotics which prioritize D2 and 5-HT2A antagonism, zicronapine possesses high affinity for the D1 receptor, a feature intended to improve cognitive and negative symptoms of schizophrenia while minimizing extrapyramidal side effects. Despite reaching Phase III clinical trials, Lundbeck announced the discontinuation of zicronapine's development in 2012, citing that the clinical data did not support a competitive profile compared to existing therapies.

Other names
zicronapine
02

Targets

DRD2 (Dopamine D2 Receptor)DRD1 (Dopamine D1 Receptor)HTR2A (Serotonin receptor 5-HT2A)

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