Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Dihydroergotamine mesylate inhalation powder is a drug-device combination product being developed by Aspeya Switzerland SA for the acute treatment of migraine. It utilizes a proprietary dry powder inhaler (DPI) to deliver dihydroergotamine (DHE), an ergot alkaloid, directly to the lungs for rapid systemic absorption. DHE acts as a potent agonist at multiple serotonin receptors, specifically 5-HT1B, 5-HT1D, and 5-HT1F, which leads to the constriction of inflamed intracranial blood vessels and the inhibition of pro-inflammatory neuropeptide release from trigeminal nerve endings. This formulation is designed to provide the rapid onset of action typically associated with intravenous administration while offering the convenience and non-invasive nature of inhalation, potentially improving patient compliance and outcomes in acute migraine management.
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 Dihydroergotamine mesylate inhalation powder.