Amolyt Pharma is a global, clinical-stage biotechnology company dedicated to developing and delivering innovative therapeutic peptides for rare endocrine and related diseases. Their primary focus is on addressing significant unmet medical needs in conditions such as hypoparathyroidism with their lead candidate eneboparatide (AZP-3601), and acromegaly with AZP-3813. The company aims to improve patient outcomes and quality of life through targeted scientific advancements. In March 2024, AstraZeneca announced an agreement to acquire Amolyt Pharma, intending to integrate it into Alexion, AstraZeneca's rare disease group.
Serves as the primary operational and research hub, overseeing European clinical development, R&D activities, and corporate functions.
Located within the Hôpital Edouard Herriot campus, specifically in 'Bâtiment Adénine – Recherche', suggesting a strong emphasis on research and close ties to clinical environments and medical expertise.
Characterized by a science-driven, innovative, and collaborative atmosphere typical of biotech firms. There's a strong focus on addressing patient needs in rare diseases, fostering a mission-oriented environment.
Lyon offers a robust biotech ecosystem, providing access to skilled talent, research collaborations, and clinical infrastructure vital for Amolyt Pharma's drug development programs.
Amolyt Pharma operates with an international scope, conducting clinical trials across multiple countries. Its physical presence is anchored by its headquarters in Lyon, France, and a key office in Cambridge, MA, USA. These locations support global functions including research and development, clinical operations, regulatory affairs, and strategic partnerships, aiming to deliver therapies for rare endocrine diseases to patients worldwide.
Hôpital Edouard Herriot, Bâtiment Adénine – Recherche, Place d’Arsonval
Lyon
Auvergne-Rhône-Alpes
France
Address: One Kendall Square, Building 1400E, Suite 14-205, Cambridge, MA 02139, USA
To advance Amolyt Pharma's clinical programs in the U.S., manage engagement with regulatory bodies such as the FDA, and leverage the rich ecosystem of talent, investment, and scientific innovation in the Boston/Cambridge area.
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As of April 2025, Amolyt Pharma' leadership includes:
Amolyt Pharma has been backed by several prominent investors over the years, including:
The most significant development concerning Amolyt Pharma's leadership and corporate structure in the last 12 months is the announcement in March 2024 of its pending acquisition by AstraZeneca. This event is expected to lead to the integration of Amolyt Pharma into AstraZeneca's rare disease unit, Alexion, which will likely influence future leadership roles. Prior to this major announcement, there were no widely publicized, distinct new hires or departures at the executive C-suite or SVP level within the preceding 12-month period.
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Amolyt Pharma likely utilizes standard corporate email address formats. Common patterns for companies in the biopharmaceutical industry include combinations of first name, last name, or initials at their domain amolytpharma.com.
[first_initial][last]@amolytpharma.com (e.g., jdoe@amolytpharma.com) or [first].[last]@amolytpharma.com (e.g., jane.doe@amolytpharma.com)
Format
t.abribat@amolytpharma.com
Example
80%
Success rate
AstraZeneca • March 14, 2024
AstraZeneca has entered into a definitive agreement to acquire Amolyt Pharma, enhancing its rare disease portfolio, Alexion, with Amolyt's promising pipeline including eneboparatide (AZP-3601) for hypoparathyroidism. The proposed acquisition includes an upfront payment of $800 million, plus a contingent payment of $250 million....more
Amolyt Pharma • November 2, 2023
Amolyt Pharma reported positive topline data from its CALYPSO Phase 2b trial of eneboparatide (AZP-3601) in hypoparathyroidism. The study met its primary endpoint, demonstrating potential to normalize calcium levels and reduce dependence on conventional therapy, supporting progression to Phase 3....more
Amolyt Pharma • June 27, 2023
The U.S. Food and Drug Administration (FDA) granted Fast Track designation to eneboparatide (AZP-3601) for the treatment of hypoparathyroidism. This designation aims to facilitate development and expedite review of therapies for serious conditions with unmet medical needs....more
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