Verve Therapeutics, Inc. (VERV): History, Ownership, Mission, How It Works & Makes Money

Verve Therapeutics, Inc. (VERV): History, Ownership, Mission, How It Works & Makes Money

US | Healthcare | Biotechnology | NASDAQ

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Could a single-course gene editing therapy truly revolutionize cardiovascular care, potentially impacting millions worldwide?

Verve Therapeutics, Inc. is boldly pursuing this vision, investing heavily in its clinical pipeline, with research and development expenses climbing past $45 million in recent quarters and maintaining a significant cash runway often exceeding $400 million to fuel its groundbreaking work in base editing for heart disease.

But how exactly did this clinical-stage company emerge, who steers its ambitious course, and what makes its approach to treating the leading cause of death so distinct?

Are you curious to understand the fundamentals—its history, ownership structure, core mission, and the innovative science driving its potential revenue streams?

Verve Therapeutics, Inc. (VERV) History

Founding Timeline

Year established

Verve Therapeutics was established in 2018.

Original location

The company was founded in Cambridge, Massachusetts, a major hub for biotechnology innovation.

Founding team members

The core founding team included leading experts in cardiovascular genetics and gene editing: Sekar Kathiresan, M.D. (who serves as CEO), Kiran Musunuru, M.D., Ph.D., M.P.H., and J. Keith Joung, M.D., Ph.D. Their collective expertise formed the scientific bedrock of the company. Understanding their driving purpose is key; explore the Mission Statement, Vision, & Core Values of Verve Therapeutics, Inc. (VERV).

Initial capital/funding

Verve launched publicly in 2019 with a substantial Series A financing round, securing $58.5 million. This initial funding was crucial for setting up operations and initiating preclinical research programs. Key investors included GV (formerly Google Ventures), ARCH Venture Partners, and F-Prime Capital.

Evolution Milestones

Year Key Event Significance
2021 Initial Public Offering (IPO) Raised gross proceeds of approximately $306.7 million, providing significant capital to advance pipeline candidates into and through clinical trials. Listed on Nasdaq under the ticker VERV.
2022 First Patient Dosed in heart-1 Trial Marked the transition to a clinical-stage company with the first human dosing of VERVE-101, its lead candidate targeting heterozygous familial hypercholesterolemia (HeFH).
2023 Positive Interim Data & VERVE-102 IND Clearance Reported encouraging initial safety and efficacy data for VERVE-101. Received FDA clearance for the Investigational New Drug (IND) application for VERVE-102, expanding the clinical pipeline.
2024 VERVE-102 Dosing Initiated & Financial Position Began dosing patients with VERVE-102, its second clinical candidate. Maintained a strong financial position, reporting cash, cash equivalents, and marketable securities of $604.1 million as of September 30, 2024, supporting ongoing development despite R&D expenses of $57.9 million in Q3 2024.

Transformative Moments

Pioneering In Vivo Base Editing for Cardiovascular Disease

The company's core strategic decision was to apply gene editing technology, specifically base editing, directly within the human body (in vivo) to target the genetic drivers of cardiovascular disease. This represented a novel and ambitious therapeutic approach, moving beyond traditional chronic therapies.

Transition to a Clinical-Stage Company

Initiating the heart-1 clinical trial in 2022 was a pivotal moment. It shifted Verve from a preclinical research entity to a clinical development organization, bringing its lead candidate, VERVE-101, into human testing and generating crucial early clinical data.

Navigating Clinical and Strategic Developments

Successfully managing the clinical development path, including addressing a temporary FDA clinical hold on VERVE-101 in the US (subsequently lifted) and advancing VERVE-102 into the clinic in 2024, demonstrated resilience. The strategic decision in 2024 to terminate the collaboration with Eli Lilly for VERVE-101 also marked a shift, focusing resources potentially more internally or towards different partnerships.

Verve Therapeutics, Inc. (VERV) Ownership Structure

As a publicly traded biotechnology company, Verve Therapeutics features a diverse ownership structure dominated by institutional investors, alongside holdings by company insiders and the general public. This composition reflects its journey from venture backing to its current status on the public markets.

Verve Therapeutics, Inc.'s Current Status

As of the end of fiscal year 2024, Verve Therapeutics, Inc. operates as a publicly traded company. Its common stock is listed on the Nasdaq Global Market under the ticker symbol VERV.

Verve Therapeutics, Inc.'s Ownership Breakdown

Ownership is concentrated among institutional holders, typical for clinical-stage biotech firms requiring significant capital. Data reflects approximate holdings based on filings towards the end of 2024.

Shareholder Type Ownership, % (Approx. End 2024) Notes
Institutional Investors ~91% Includes mutual funds, pension funds, venture capital firms (like ARCH Venture Partners, GV), and other large investment managers. Significant holdings reflect confidence in the company's gene editing platform.
Company Insiders ~4% Includes shares held by executive officers, directors, and co-founders. Aligns leadership interests with shareholder value.
Public & Other ~5% Represents shares held by individual retail investors and entities not classified as institutions or insiders.

Verve Therapeutics, Inc.'s Leadership

Guiding the company's strategic direction and operations requires experienced leadership, crucial for navigating the complex biotech landscape. The team's expertise is vital for executing the Mission Statement, Vision, & Core Values of Verve Therapeutics, Inc. (VERV). Key figures steering the company as of the end of 2024 include:

  • Sekar Kathiresan, M.D. - Co-founder and Chief Executive Officer
  • Andrew Ashe - President and Chief Operating Officer
  • Allison Dorval - Chief Financial Officer
  • Andrew Bellinger, M.D., Ph.D. - Chief Scientific Officer & Chief Medical Officer

This leadership team combines deep scientific knowledge with extensive operational and financial experience in the biopharmaceutical industry.

Verve Therapeutics, Inc. (VERV) Mission and Values

Verve Therapeutics is driven by a clear purpose focused on tackling cardiovascular disease through genetic medicine. Understanding their core principles offers insight into their long-term goals and operational philosophy, which is crucial when evaluating their potential, as discussed in Breaking Down Verve Therapeutics, Inc. (VERV) Financial Health: Key Insights for Investors.

Verve Therapeutics, Inc. (VERV) Core Purpose

Official mission statement

To protect the world from cardiovascular disease.

Vision statement

While a distinct, separate vision statement isn't prominently published, the company's ambitious mission itself outlines a clear long-term vision: a future where cardiovascular disease is preventable through their innovative therapies.

Company slogan

Verve Therapeutics does not appear to utilize a specific, widely marketed company slogan.

Core Values

Guiding their work and culture, Verve emphasizes several key values:

  • Patients First: Prioritizing the needs and well-being of patients above all else.
  • Urgency: Recognizing the critical need for new treatments and acting with speed and focus.
  • Collaboration: Fostering teamwork internally and externally to achieve shared goals.
  • Excellence: Striving for the highest standards in science, research, and execution.
  • Integrity: Operating with ethical principles and transparency in all endeavors.

Verve Therapeutics, Inc. (VERV) How It Works

The company pioneers gene editing medicines designed as single-course treatments to durably lower disease-causing proteins for cardiovascular disease. It leverages in vivo base editing technology to make precise, protective edits to the genome in targeted cells, primarily within the liver.

The Company's Product/Service Portfolio

Product/Service Target Market Key Features
VERVE-101 Heterozygous Familial Hypercholesterolemia (HeFH) patients with established atherosclerotic cardiovascular disease (ASCVD) Investigational in vivo base editing medicine targeting the PCSK9 gene in the liver to lower LDL cholesterol.
VERVE-102 Patients with established ASCVD not adequately controlled on oral therapy Investigational in vivo base editing medicine targeting the PCSK9 gene, using a different lipid nanoparticle (LNP) delivery system.
VERVE-201 Homozygous Familial Hypercholesterolemia (HoFH) Investigational in vivo base editing medicine targeting the ANGPTL3 gene in the liver to lower LDL cholesterol and triglycerides.

The Company's Operational Framework

Operations revolve around extensive research and development (R&D) activities, forming the core of value creation. This includes discovery research, preclinical studies, and advancing lead candidates through clinical trials, such as the ongoing Phase 1b trials for VERVE-101 initiated in 2024. Manufacturing of the complex gene editing components and delivery systems, often involving specialized contract development and manufacturing organizations (CDMOs), is critical. The company also engages heavily in regulatory affairs, seeking guidance and approvals from bodies like the FDA and EMA. Strategic collaborations, notably with Beam Therapeutics for base editing technology and Eli Lilly for certain LNP delivery technology and development support, are integral to the operational model. Significant capital fuels these efforts; R&D expenses alone reached approximately $149.7 million for the first nine months of 2024, reflecting the high cost of developing novel genetic medicines. Understanding the financial structure supporting these operations is vital; you can explore this further here: Breaking Down Verve Therapeutics, Inc. (VERV) Financial Health: Key Insights for Investors. As of September 30, 2024, the company maintained a solid financial position with cash, cash equivalents, and marketable securities totaling $547.5 million to fund these ongoing operations.

The Company's Strategic Advantages

Several factors contribute to the company's competitive positioning in the biopharmaceutical landscape.

  • Pioneering Technology: Its focus on in vivo base editing, a precise form of gene editing potentially offering advantages over traditional CRISPR-Cas9 nuclease approaches, represents a key scientific differentiator.
  • Cardiovascular Focus: Targeting cardiovascular disease, a leading cause of death globally with significant unmet needs, addresses a vast potential market.
  • Single-Course Treatment Potential: The goal of creating durable, potentially lifelong effects from a single administration offers a transformative value proposition compared to chronic therapies.
  • Strategic Partnerships: Collaborations provide access to essential technology, development expertise, and potential future commercialization pathways, mitigating some risks inherent in biotech development.
  • Experienced Leadership: The management team possesses deep expertise in genetic medicine, drug development, and cardiovascular disease, guiding strategic direction.

Verve Therapeutics, Inc. (VERV) How It Makes Money

As a clinical-stage biotechnology company, Verve Therapeutics primarily generates revenue through collaboration agreements with larger pharmaceutical companies, focusing on developing its gene editing therapies. It does not yet have commercial product sales and relies on upfront payments, research funding, and potential future milestone payments and royalties from these partnerships.

Verve Therapeutics, Inc.'s Revenue Breakdown

Revenue Stream % of Total Growth Trend
Collaboration Revenue 100% Increasing
Product Sales 0% N/A

Verve Therapeutics, Inc.'s Business Economics

The economic model for Verve is typical of a pre-commercial biotech firm, characterized by substantial investment in research and development aimed at bringing novel therapies through rigorous clinical trials and regulatory approval processes. Key cost drivers include:

  • Clinical trial execution and management.
  • Preclinical research and discovery activities.
  • Personnel costs for scientific and administrative staff.
  • Manufacturing process development for potential therapies.

Profitability hinges entirely on the future successful commercialization of its product candidates or potentially lucrative licensing deals. Until then, the company's operations are funded through equity financing and collaboration payments. The value proposition rests on the potential of its gene editing technology to provide one-time cures for cardiovascular diseases, representing a significant market opportunity if successful.

Verve Therapeutics, Inc.'s Financial Performance

As of late 2024, Verve Therapeutics' financial profile reflects its clinical-stage status. For the nine months ended September 30, 2024, the company reported collaboration revenue of approximately $10.1 million, primarily related to its agreements with major pharmaceutical partners. However, operating expenses remain high due to ongoing research and development efforts. R&D expenses for the same period were $140.8 million, while General and Administrative (G&A) expenses totaled $43.7 million. This resulted in a net loss of $174.4 million for the first nine months of 2024. The company maintained a strong cash position, holding $646.8 million in cash, cash equivalents, and marketable securities as of September 30, 2024, providing operational runway for continued development activities. For a deeper dive, consider Breaking Down Verve Therapeutics, Inc. (VERV) Financial Health: Key Insights for Investors. The company's financial health is closely tied to clinical progress and its ability to manage cash burn effectively while advancing its pipeline towards potential commercialization.

Verve Therapeutics, Inc. (VERV) Market Position & Future Outlook

The company is carving out a unique position by pioneering *in vivo* base editing therapies specifically targeting cardiovascular disease drivers, a potentially massive market. Its future hinges critically on demonstrating clinical safety and efficacy in ongoing trials for its lead candidates.

Competitive Landscape

The gene editing field is dynamic, with several players employing different technologies and targeting various diseases. While direct market share is not applicable for clinical-stage companies, relative positioning reflects technological focus and pipeline progress.

Company Relative Position Proxy (%) Key Advantage
The Company ~15-25% (in *in vivo* base editing for CVD) Pioneer in base editing for Atherosclerotic Cardiovascular Disease (ASCVD); Focused pipeline (VERVE-101, VERVE-102).
Intellia Therapeutics (NTLA) ~30-40% (Broader *in vivo* CRISPR) Leading *in vivo* CRISPR-Cas9 data (e.g., ATTR amyloidosis); Broader platform application.
CRISPR Therapeutics (CRSP) ~25-35% (Ex-vivo focus, broadening) First approved CRISPR therapy (Casgevy, *ex vivo*); Established platform; Expanding into *in vivo*.
Beam Therapeutics (BEAM) ~15-25% (Base editing platform) Broad base editing platform technology; Diverse pipeline across *ex vivo* and *in vivo* applications.

Note: Percentages are conceptual estimates reflecting leadership and focus within specific niches of the gene editing market as of late 2024/early 2025, not established revenue-based market share.

Opportunities & Challenges

Opportunities Risks
Successful Phase 1b data readout for VERVE-101 and advancing VERVE-102 could significantly de-risk the platform. Potential for off-target edits or unforeseen long-term safety issues with base editing technology.
Validation of base editing as a therapeutic modality opens doors for pipeline expansion to other genetic cardiovascular risk factors. Regulatory pathway for *in vivo* gene editing therapies, especially germline editing concerns, remains complex and evolving.
Partnerships, like the one with Eli Lilly for VERVE-201, provide validation and non-dilutive funding (Lilly collaboration provided significant upfront and potential milestone payments). High cash burn rate associated with clinical trials and R&D (Net loss was $81.9 million for Q3 2024); Future funding needs depend heavily on clinical success. Breaking Down Verve Therapeutics, Inc. (VERV) Financial Health: Key Insights for Investors
Addressing large unmet needs in heterozygous familial hypercholesterolemia (HeFH) and homozygous familial hypercholesterolemia (HoFH) represents a substantial market opportunity. Intense competition from other gene editing companies and established standard-of-care therapies for cardiovascular disease.

Industry Position

This enterprise stands as a clinical-stage biotechnology firm specializing in the development of single-course gene editing medicines aimed at cardiovascular disease. Its core differentiation lies in the application of base editing technology for *in vivo* treatments, aiming to permanently turn off genes associated with conditions like high LDL cholesterol.

As of early 2025, its position is that of an innovator navigating the critical stages of clinical development. Success is heavily tied to the outcomes of its lead programs, VERVE-101 and VERVE-102. The company's substantial cash reserves ($568.4 million as of September 30, 2024) provide runway, but sustained progress and positive data are essential to maintain investor confidence and secure its place against larger, more diversified competitors in the rapidly evolving gene therapy landscape.

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