Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
DPI-289 is a novel, orally bioavailable small molecule designed as a bi-functional opioid modulator, acting as a **delta opioid receptor agonist** and a **mu opioid receptor antagonist** (DAMA). It is under development primarily for **Parkinson's disease**, targeting motor symptoms and aiming to reduce L-DOPA-induced dyskinesia and L-DOPA dose requirements. Preclinical studies in rodent and non-human primate models demonstrate antiparkinsonian efficacy without inducing dyskinesia, with DPI-289 enhancing the benefit of L-DOPA while potentially minimizing side effects seen with standard dopaminergic therapies. The compound is being developed by Eboo Pharmaceuticals, with key research conducted in collaboration with Atuka Inc. and Dina Pharmaceuticals[1][3][4][5].
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 DPI-289.