Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
AR1005 is a fixed-dose combination (FDC) drug candidate being developed by AriBio for the treatment of Lewy body disease (LBD), including dementia with Lewy bodies. The product combines mirodenafil (also known as AR1001), a selective phosphodiesterase 5 (PDE5) inhibitor, with rivastigmine, a dual acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitor that is a standard-of-care treatment for LBD. Mirodenafil is intended to enhance the nitric oxide (NO)/cGMP signaling pathway, promoting neuroprotection, synaptic plasticity, and improved cerebral blood flow, while rivastigmine addresses the cholinergic deficit characteristic of the disease. By combining these two mechanisms, AR1005 aims to provide synergistic improvements in cognitive function, behavioral psychological symptoms, and motor fluctuations. The drug is currently being evaluated in a Phase 2a clinical trial (NCT06537076) in patients with cognitive impairment due to Lewy body disease.
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 mirodenafil + rivastigmine.