Why Inhalation?

Significant unmet
needs still exist today

Oral drugs represent ~90% of all pharmaceuticals but are associated with limitations for both patients and drug developers, including:

Significant unmet
needs still exist today

Oral drugs represent ~90% of all pharmaceuticals but are associated with limitations for both patients and drug developers, including:

Side Effects

Oral drugs pass through the GI tract and are largely metabolized in the liver, increasing side effects and reducing bioavailability.1

Bioavailability

Poor bioavailability creates a major drug development hurdle, including high drug failure rates in clinical trials2 and poor drug delivery for lung diseases.3

Drug Failures

Liver toxicity accounts for
1 in 4.5 clinical drug failures and 1 in 3 market withdrawals from adverse drug reactions.4

Inhalation unlocks
therapeutic potential

Inhalation enables rapid and efficient drug delivery, providing multiple potential benefits:

Discover the power of our inhalation platforms

Discover the power of our inhalation platforms

Development requires highly specialized skills and equipment

Developing inhaled therapeutics is out-of-reach for most companies due to the complexity and challenges it poses, including:

Requires highly specialized expertise on inhalable formulations and complex drug-device development

Manufacturing requires expensive, high-volume, custom equipment

Must navigate more stringent regulatory requirements for drug-device combinations 

Explore how we've addressed these industry challenges

1. Bashiardes S, Christodoulou C. Orally Administered Drugs and Their Complicated Relationship with Our Gastrointestinal Tract. Microorganisms. 2024;12(2):242. Published 2024 Jan 24. doi:10.3390/microorganisms12020242
2. Wu K, Kwon SH, Zhou X, et al. Overcoming Challenges in Small-Molecule Drug Bioavailability: A Review of Key Factors and Approaches. Int J Mol Sci. 2024;25(23):13121. Published 2024 Dec 6. doi:10.3390/ijms252313121.
3. Newman SP. Drug delivery to the lungs: challenges and opportunities. Ther Deliv. 2017;8(8):647-661. doi:10.4155/tde-2017-0037.
4. Watkins PB. Drug safety sciences and the bottleneck in drug development. Clin Pharmacol Ther. 2011;89(6):788-790. doi:10.1038/clpt.2011.63