Verve Therapeutics, Inc. (VERV)

US — Healthcare Sector
Peers: ADPT  BEAM  CRBU  SANA  NTLA  EDIT  CRSP  PRME  THRX  LIFE  RLAY  IPSC  BPMC 

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Key Metrics & Ratings

  • symbol VERV
  • Rev/Share 0.6862
  • Book/Share 5.4506
  • PB 0.8164
  • Debt/Equity 0.145
  • CurrentRatio 9.843
  • ROIC -0.3643

 

  • MktCap 396687240.0
  • FreeCF/Share -1.6919
  • PFCF -2.6989
  • PE -2.1358
  • Debt/Assets 0.1118
  • DivYield 0
  • ROE -0.3582

 

  • Rating C+
  • Score 2
  • Recommendation Sell
  • P/E Score 1
  • DCF Score 3
  • P/B Score 4
  • D/E Score 3

Recent Analyst Ratings

Type Ticker Analyst Firm Previous Rating Current Rating Previous Price Target Current Price Target Date
Upgrade VERV Cantor Fitzgerald Neutral Overweight -- -- April 15, 2025

News

3 Top Genomics Stocks to Add to Your Portfolio in 2025
NTLA, QURE, VERV
Published: May 21, 2025 by: Zacks Investment Research
Sentiment: Neutral

Investors interested in the Genomics and Synthetic Biology theme may consider adding these three stocks to their portfolio - Intellia Therapeutics (NTLA), uniQure (QURE) and Verve Therapeutics (VERV).

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image for news 3 Top Genomics Stocks to Add to Your Portfolio in 2025
Verve Therapeutics (VERV) Reports Q1 Loss, Tops Revenue Estimates
VERV
Published: May 14, 2025 by: Zacks Investment Research
Sentiment: Negative

Verve Therapeutics (VERV) came out with a quarterly loss of $0.35 per share versus the Zacks Consensus Estimate of a loss of $0.71. This compares to loss of $0.59 per share a year ago.

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image for news Verve Therapeutics (VERV) Reports Q1 Loss, Tops Revenue Estimates
Verve Therapeutics: FDA Fast Track And Eli Lilly Partnership Upgrade It To A 'Buy'
LLY, VERV
Published: April 16, 2025 by: Seeking Alpha
Sentiment: Positive

VERV's VERVE-102 showed an impressive 69% LDL-C reduction in its early Phase 1b data. Also, LLY may opt into VERVE-102's development later this year, which would help VERV by covering one-third of the R&D costs. Similarly, VERV's pipeline includes VERVE-201 for HoFH and refractory hypercholesterolemia, as well as VERVE-301 in collaboration with Lilly.

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image for news Verve Therapeutics: FDA Fast Track And Eli Lilly Partnership Upgrade It To A 'Buy'
VERV Stock Soars on Superior Efficacy in Phase I Cholesterol Study
VERV
Published: April 15, 2025 by: Zacks Investment Research
Sentiment: Positive

Verve Therapeutics stock rises on demonstrating superior LDL-C lowering ability in a phase Ib study of VERVE-102 in patients with HeFH and/or CAD.

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image for news VERV Stock Soars on Superior Efficacy in Phase I Cholesterol Study
Why Verve Therapeutics Is Skyrocketing Today
VERV
Published: April 15, 2025 by: The Motley Fool
Sentiment: Positive

Verve Therapeutics (VERV 22.57%) stock is seeing explosive gains Tuesday. The biotech company's share price was up 24.5% as of 12:30 p.m.

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image for news Why Verve Therapeutics Is Skyrocketing Today
Verve Therapeutics Touts Positive Data From Gene Editing Medicine To Lower Cholesterol After Single Dose
VERV
Published: April 14, 2025 by: Benzinga
Sentiment: Positive

Verve Therapeutics Inc VERV on Monday released initial data from the Heart-2 Phase 1b trial of VERVE-102 in patients with heterozygous familial hypercholesterolemia (HeFH) and/or premature coronary artery disease (CAD), which requires reducing low-density lipoprotein cholesterol (LDL-C) levels in the blood.

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image for news Verve Therapeutics Touts Positive Data From Gene Editing Medicine To Lower Cholesterol After Single Dose
Verve Therapeutics Announces Clearance of Investigational New Drug Application by the U.S. FDA for VERVE-102, an Investigational Gene Editing Medicine Designed to Durably Lower Cholesterol After a Single Dose
VERV
Published: March 24, 2025 by: GlobeNewsWire
Sentiment: Neutral

BOSTON, March 24, 2025 (GLOBE NEWSWIRE) -- Verve Therapeutics, a clinical-stage company developing a new class of genetic medicines for cardiovascular disease, today announced the clearance of its Investigational New Drug (IND) application by the U.S. Food and Drug Administration (FDA) for VERVE-102 for the treatment of patients living with heterozygous familial hypercholesterolemia (HeFH) and/or premature coronary artery disease (CAD). VERVE-102 is a novel, investigational in vivo base editing medicine designed to be a single-course treatment that inactivates the PCSK9 gene in the liver to durably lower blood low-density lipoprotein cholesterol (LDL-C).

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image for news Verve Therapeutics Announces Clearance of Investigational New Drug Application by the U.S. FDA for VERVE-102, an Investigational Gene Editing Medicine Designed to Durably Lower Cholesterol After a Single Dose
Verve Therapeutics Announces Pipeline Progress and Reports Fourth Quarter and Full Year 2024 Financial Results
VERV
Published: February 27, 2025 by: GlobeNewsWire
Sentiment: Neutral

Initial data from the Heart-2 Phase 1b clinical trial of VERVE-102 targeting PCSK9 expected in the second quarter of 2025, with final dose escalation data in the second half of 2025

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image for news Verve Therapeutics Announces Pipeline Progress and Reports Fourth Quarter and Full Year 2024 Financial Results

About Verve Therapeutics, Inc. (VERV)

  • IPO Date 2021-06-17
  • Website https://www.vervetx.com
  • Industry Biotechnology
  • CEO Dr. Sekar Kathiresan M.D.
  • Employees 274

Verve Therapeutics, Inc., a genetic medicines company, engages in developing gene editing medicines for patients to treat cardiovascular diseases. Its lead product candidate is VERVE-101, a single-course gene editing treatment that permanently turns off the PCSK9 gene in the liver. The company also engages in the development of ANGPTL3 program to permanently turn off the ANGPTL3 gene in the liver. It has a collaboration and license agreement with Beam Therapeutics Inc.; a development and option agreement with Acuitas Therapeutics, Inc.; and a Cas9 license agreement with The Broad Institute and the President and Fellows of Harvard College. The company was formerly known as Endcadia, Inc. and changed its name to Verve Therapeutics, Inc. in January 2019. Verve Therapeutics, Inc. was incorporated in 2018 and is headquartered in Cambridge, Massachusetts.