Drug intelligence / Profile preview

ciladopa

Development stage
Discontinued
Lead developer
Pfizer
Modality
Small Molecules
Administration
Oral
01

Overview

Ciladopa is a small molecule dopamine agonist, specifically a troponylpiperazine derivative, that was developed for the treatment of Parkinson's disease. It acts primarily as an agonist at dopamine D2-like receptors, mimicking the action of endogenous dopamine to alleviate motor symptoms such as bradykinesia, rigidity, and gait disturbances. In clinical evaluations, ciladopa demonstrated the ability to improve disability scores and allow for a reduction in the required dose of levodopa (Sinemet). Despite its initial clinical promise and relatively low incidence of acute adverse effects, its development was discontinued by Ayerst Laboratories in the mid-1980s, primarily due to findings of potential carcinogenicity (specifically Leydig cell tumors) in long-term rodent toxicity studies.

Other names
ciladopa hydrochloride
02

Targets

DRD2 (Dopamine D2 Receptor)

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