Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Lubabegron, marketed under the brand name Experior, is a veterinary pharmaceutical drug approved for use in beef cattle. It is the first FDA-approved product specifically labeled to reduce ammonia gas emissions from an animal or its waste. Lubabegron acts as a beta-adrenergic receptor agonist/antagonist (β-AAA), with antagonist activity at β1 and β2 receptors and agonist activity at β3 receptors. This unique mechanism allows it to reduce ammonia emissions without causing the negative side effects associated with other beta-agonists that stimulate β1 and β2 receptors. The drug is administered to beef steers and heifers fed in confinement for slaughter during their final 14 to 91 days on feed. Its primary benefit is environmental stewardship by reducing ammonia gas released from manure, which can contribute to atmospheric haze, noxious odors, and eutrophication of water bodies[3][7][8].
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 lubabegron.