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Verve Therapeutics Founded to Protect Against Heart Disease Launches with $58.5 Million in Series A

Company to Develop Gene Editing Therapies to Permanently Reduce Risk of Coronary Artery Disease in Adults


Announces Key Licensing Agreements with the Broad Institute and Harvard University, and Collaboration Agreements with Beam Therapeutics and Verily


Leading Cardiologist and Geneticist Sekar Kathiresan, M.D., Named Chief Executive Officer


CAMBRIDGE, Mass. — May 7, 2019 — Verve Therapeutics, a next-generation cardiovascular company, today announced its launch to discover and develop therapies that safely edit the adult human genome to permanently reduce a person’s risk of coronary artery disease, the most common form of heart disease and the leading cause of death worldwide. Verve brings together two of the biggest breakthroughs in 21st-century biomedicine — human genetic analysis and gene editing — to create a promising new treatment approach for adults at risk of coronary artery disease. The company was founded by a team of world-renowned researchers in cardiovascular genetics and pioneers of gene editing, including Sekar Kathiresan, M.D., Kiran Musunuru, M.D., Ph.D., MPH, and J. Keith Joung, M.D., Ph.D.


The $58.5 million Series A financing was led by GV (formerly Google Ventures), with participation from ARCH Venture Partners, F-Prime Capital, and Biomatics Capital. The funds raised will be used to advance the pre-clinical programs through proof-of-concept studies. The company has assembled a portfolio of key gene editing technologies, which includes a collaboration with Beam Therapeutics and license agreements with Harvard University and the Broad Institute of MIT and Harvard. Verve has also entered into a collaboration with Verily to develop and optimize nanoparticle formulations for therapeutic delivery.


Genetic research conducted by Verve’s founders and others has identified healthy adults who carry naturally occurring gene variants that dramatically lower their lifetime risk of coronary artery disease and heart attacks. Verve is building on this research to develop gene editing therapies that confer lifelong protection in adults at risk of coronary artery disease.


All of the therapeutics to be developed by Verve involve making edits in adult (somatic) cells, which are not passed down to offspring.


“Coronary artery disease is a true pandemic and a growing health crisis,” said Sekar Kathiresan, M.D., co-founder and incoming chief executive officer of Verve. “Our genetic understanding of coronary artery disease, combined with increasing sophistication of gene editing technologies, have aligned to create a transformative moment in the treatment of this disease. Verve was founded to turn the tide of coronary artery disease worldwide. Gene editing offers the possibility of introducing protective gene variants to adults at risk of the disease through a one-time therapy.”


“New therapeutic approaches are needed to protect populations at risk of coronary artery disease,” said Kiran Musunuru, M.D., Ph.D., MPH, co-founder and chief scientific advisor of Verve and associate professor of cardiovascular medicine and genetics at the Perelman School of Medicine at University of Pennsylvania. “Gene editing has the potential to completely transform the treatment paradigm for the disease. Preclinical studies conducted in the field, including work done in my lab, have shown the promise of gene editing to safely reduce cholesterol and other coronary artery disease risk factors.”

Existing treatments to prevent coronary artery disease, including cholesterol-lowering statins and other therapies, face challenges due to poor adherence, high cost, and limited access to these medicines, especially in low- and middle-income countries, where more than 80 percent of deaths due to coronary artery disease occur.1

Gene editing technologies, including CRISPR nucleases and base editors, have the potential to change those outcomes. Accurate, directed gene edits within the adult liver could improve lifelong lipid and metabolic status and lower coronary artery disease risk. Preclinical studies already conducted by the company and its scientific founders have validated the potential efficacy of gene editing approaches to safely reduce coronary artery disease risk factors.


Verve will take a stepwise approach to clinical development, first taking aim at patients with life-threatening coronary artery disease and high unmet medical need. As the company establishes safety and efficacy, Verve will widen its clinical focus to include progressively larger patient populations at risk of coronary artery disease.


“Cholesterol-lowering treatments have been an important advance for many patients at risk of coronary artery disease,” said Burt Adelman, M.D., co-founder and chairman of the board of Verve. “However, as the disease’s prevalence rises in low- and middle-income countries, the current treatment model of daily pills or monthly injections over a lifetime must evolve if we are to effectively protect millions of people from disability or death due to coronary artery disease. Imagine if a single injection could permanently and safely prevent coronary disease. That’s the singular goal that Verve will be pursuing.”


To Read More: https://www.vervetx.com/press-releases/verve-therapeutics-founded-to-protect-against-heart-disease-launches-with-58-5-million-in-series-a-funding-led-by-gv/