Verve Therapeutics to Participate in the Guggenheim Genomic Medicines and Rare Disease Conference
Verve Therapeutics, a biotechnology company focused on cardiovascular disease treatment, has announced that its Chief Scientific Officer, Dr. Andrew Bellinger, will participate in a fireside chat at the Guggenheim Genomic Medicines and Rare Disease Conference on March 31, 2022, at 10:00 a.m. ET. The event will be available via a live webcast on the company's investor website and archived for 60 days. Verve is known for its innovative gene editing medicines, including its lead product candidate, VERVE-101, aimed at permanently reducing LDL cholesterol levels to mitigate cardiovascular disease risk.
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CAMBRIDGE, Mass., March 24, 2022 (GLOBE NEWSWIRE) -- Verve Therapeutics, a biotechnology company pioneering a new approach to the care of cardiovascular disease with single-course gene editing medicines, today announced that Andrew Bellinger, M.D., Ph.D., chief scientific officer and chief medical officer, will participate in a fireside chat during the virtual Guggenheim Genomic Medicines and Rare Disease Conference on Thursday, March 31, 2022 at 10:00 a.m. ET.
A live webcast will be available in the investor section of the company's website at www.vervetx.com. The webcast will be archived for 60 days following the presentation.
About Verve Therapeutics
Verve Therapeutics, Inc. (Nasdaq: VERV) is a genetic medicines company pioneering a new approach to the care of cardiovascular disease, transforming treatment from chronic management to single-course gene editing medicines. The company’s initial two programs target PCSK9 and ANGPTL3, genes that have been extensively validated as targets for lowering blood lipids such as low-density lipoprotein cholesterol (LDL-C), a root cause of cardiovascular disease. Verve’s lead product candidate, VERVE-101, is designed to permanently turn off the PCSK9 gene in the liver in order to disrupt blood PCSK9 protein production and thereby durably reduce blood LDL-C levels, with the goal of reducing a patient’s risk for cardiovascular disease. VERVE-101, currently in IND-enabling studies, is being developed initially for the treatment of patients with heterozygous familial hypercholesterolemia, a potentially fatal genetic heart disease. For more information, please visit www.VerveTx.com.
Investor Contact
Jen Robinson
Verve Therapeutics, Inc.
jrobinson@vervetx.com
Media Contact
Gina Nugent
Ten Bridge Communications
gina@tenbridgecommunications.com
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