Regio Biosciences Enters into License Agreement with AstraZeneca for Phase 2a Asset in Peripheral Artery Disease (PAD)
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Thursday, February 3, 2022
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Regio expects to initiate a Phase 2a clinical program evaluating REG-101 in PAD during the second half of 2022.
Key Points:
- Regio expects to initiate a Phase 2a clinical program evaluating REG-101 in PAD during the second half of 2022.
- The Regio team is thrilled to announce the signing of this license agreement with AstraZeneca to further develop REG-101, said Chris Jeffers, Chairman of Regio Biosciences and CEO of Hibiscus BioTechnology.
- We believe that REG-101 could complement the current standard of care as a patient-centric, once-monthly injection for peripheral artery disease.
- Regio has partnered with CPC Clinical Research (CPC) and multiple clinical sites in the US to conduct a Phase 2a clinical trial in patients with peripheral artery disease.