Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
K-3505 is an orally administered, gut-restricted small molecule therapeutic developed by Kallyope, Inc. for the treatment of migraine. Utilizing Kallyope's proprietary platform focused on the gut-brain axis, K-3505 is designed to act locally within the gastrointestinal tract to modulate neural or hormonal signaling pathways—potentially involving 5-HT3 receptors—that communicate with the brain to influence migraine pathophysiology. By remaining gut-restricted, the compound aims to provide therapeutic benefit while avoiding the systemic exposure and associated side effects typical of other migraine medications. Clinical development progressed to Phase 1 trials in Australia; however, a planned Part II study to further assess safety, pharmacokinetics, and pharmacodynamics in healthy volunteers was withdrawn in 2023 due to a change in the sponsor's development strategy, and the asset is no longer a primary focus of the company's active clinical pipeline.
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 K-3505.