Toward the Development of a Commercial Process to Produce Muvalaplin. Part II: Preparation of the Drug Substance
Abstract Herein, we describe the development of steps 5–7 for a large-scale process to synthesize muvalaplin, a small-molecule lipoprotein(a) inhibitor for the potential reduction of major adverse cardiovascular events in participants with established cardiovascular disease or at risk for a first cardiovascular event. Each step was optimized, leading to improvements in safety, robustness, and cost of goods that ultimately resulted in a 41% yield increase over three steps and a 60% reduction in PMI compared to the original discovery synthesis. The process was safely scaled to >100 kg, thus ensuring clinical supply and laying the foundation for a commercial route.
Authors
- Matthew J. Genzink (ORCID: https://orcid.org/0000-0002-8956-5635)
- Srinivas Gangula (ORCID: https://orcid.org/0000-0002-3765-6877)
- Jianfei Dai
- Daniel P. Walker (ORCID: https://orcid.org/0009-0001-7703-5936)
- Dajiang Jing
- John R. Rizzo (ORCID: https://orcid.org/0009-0009-7950-5290)
- Antonio Navarro (ORCID: https://orcid.org/0000-0002-3623-0946)
- Silong Zhang
- Mai Khanh Hawk
- Panpan Sun
Institutions
- Eli Lilly (United States) (US)
Publication Details
- Journal
- Organic Process Research & Development
- Published
- 2026-09-22
- DOI
- https://doi.org/10.1021/acs.oprd.6c00323
- Primary Topic
- Lipoproteins and Cardiovascular Health
- Type
- article
- Field-Weighted Citation Impact
- 0.00