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

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

US | Healthcare | Biotechnology | NASDAQ

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RAPT Therapeutics, Inc. is a clinical-stage biopharma company, but are they just another name in the crowded immunology space, or a defintely genuine disruptor?

Their distinctive focus on developing novel oral small-molecule therapies for inflammatory diseases like food allergy and chronic spontaneous urticaria (CSU) is starting to show tangible clinical progress, with their lead candidate, ozureprubart, initiating a key Phase 2b trial in late 2025. Financially, the company is managing its clinical burn rate effectively, reporting a net loss of only $52.4 million for the first nine months of the 2025 fiscal year, a significant improvement from the prior year.

Plus, their recent October 2025 public offering secured approximately $234.4 million in net capital, extending their operating runway into mid-2028-so how exactly will a clinical-stage entity generate revenue and turn that clinical promise into a commercial win before the cash runs out?

RAPT Therapeutics, Inc. (RAPT) History

You need to understand where RAPT Therapeutics came from to judge its clinical-stage risk and runway, and the story begins with a strategic pivot. The company was defintely not born as RAPT, but as a venture-backed effort to translate cutting-edge immunology into new medicines.

Given Company's Founding Timeline

Year established

The company was incorporated in March 2015 under the initial name FLX Bio, Inc..

Original location

South San Francisco, California, which is the heart of the US biotech industry.

Founding team members

The initial team included experienced scientific leaders and venture capitalists. Key early figures who joined in 2015 included Brian Wong, M.D., Ph.D., who became President and CEO, and William Ho, M.D., Ph.D., who joined as Chief Medical Officer.

Initial capital/funding

RAPT launched with substantial venture capital support, including a Series B funding round in 2017 that raised around $60 million. Total funding raised across all rounds, including venture and public offerings, has reached over $199 million as of late 2024.

Given Company's Evolution Milestones

Year Key Event Significance
2018 Rebranded from FLX Bio, Inc. to RAPT Therapeutics, Inc. Signaled a refined, public-facing focus on its pipeline of oral small molecule therapies for inflammation and oncology.
2019 Initial Public Offering (IPO) on Nasdaq (RAPT) Raised approximately $36.0 million in gross proceeds, providing the first major capital infusion from public markets to advance clinical programs.
2025 Positive topline Phase 2 data for ozureprubart in Chronic Spontaneous Urticaria (CSU) Demonstrated comparable efficacy and safety to a major existing therapy (omalizumab), validating the drug's potential in a large inflammatory market.
2025 Completed underwritten public offering in October Raised approximately $250.0 million in gross proceeds, significantly extending the company's cash runway to mid-2028.

Given Company's Transformative Moments

The company's history is a series of calculated steps to de-risk its pipeline and secure capital. The shift from FLX Bio to RAPT Therapeutics in 2018 was more than a name change; it was a clear signal of moving from foundational research toward clinical execution in inflammation and oncology.

The October 2025 public offering was the most recent game-changer. Raising $250.0 million in gross proceeds at $30.00 per share, as they did, provides a huge financial cushion for a clinical-stage company. This capital is the lifeblood for a biotech firm, especially since the net loss for the nine months ended September 30, 2025, was still substantial at $52.4 million.

  • Pipeline Validation: The positive Phase 2 data for ozureprubart (formerly RPT904) in CSU in 2025, showing it was comparable to a leading injectable drug, immediately boosted its value and potential.
  • Strategic Focus: Following the positive data, the FDA cleared an Investigational New Drug (IND) application, allowing RAPT to start a Phase 2b trial for ozureprubart in food allergy, which is a massive and underserved market. This new trial, initiated in 2025, is a major commitment.
  • Financial Runway: The October 2025 financing is projected to fund operations until mid-2028, giving the team a crucial three-year window to hit more clinical milestones without immediate capital pressure. That's a strong position to be in.

The story of RAPT is about translating early science into late-stage clinical assets and then funding that push with timely, large equity raises. You can dive deeper into the institutional backing and strategy with Exploring RAPT Therapeutics, Inc. (RAPT) Investor Profile: Who's Buying and Why?

RAPT Therapeutics, Inc. (RAPT) Ownership Structure

RAPT Therapeutics, Inc. is controlled overwhelmingly by institutional investors, a common structure for a clinical-stage biotechnology company, with a small fraction held by company insiders. This means the strategic direction is heavily influenced by large funds focused on long-term growth in the biotech sector.

Given Company's Current Status

RAPT Therapeutics is a publicly traded, clinical-stage biopharmaceutical company, with its common stock listed and trading on the Nasdaq Stock Market (NasdaqGM) under the ticker symbol RAPT. As of November 2025, the company's market capitalization stands at approximately $750.4 million. To be fair, the company faced a Nasdaq minimum bid price deficiency notice in May 2025, which it was working to cure by November 17, 2025, though it remains listed.

The company recently completed a significant financing round, an underwritten public offering in October 2025, raising gross proceeds of approximately $250.0 million. This capital injection is defintely a huge tailwind for their clinical programs, like the lead candidate RPT904. You can read more about their core strategy here: Mission Statement, Vision, & Core Values of RAPT Therapeutics, Inc. (RAPT).

Given Company's Ownership Breakdown

The ownership is highly concentrated among institutional players, which is typical for a company relying on significant capital for drug development. Institutional investors hold the vast majority of the shares, giving them outsized voting power in key corporate decisions.

Shareholder Type Ownership, % Notes
Institutional Investors 82.07% Includes major holders like OrbiMed Advisors, TCG Crossover Management, and Vanguard Group Inc.
Retail/Public Float 17.51% Shares held by individual investors and the general public.
Insiders (Executives & Directors) 0.42% Direct holdings by management and board members.

It's important to note that the top institutional holders alone often represent a significant portion of the institutional stake. For instance, Medicxi Ventures and Forbion Growth Opportunities Fund III Cooperatief U.A. are among the largest shareholders.

Given Company's Leadership

The company is steered by an experienced leadership team with a deep background in immunology and drug development, balancing scientific expertise with financial oversight. The average tenure for the management team is about 4.6 years, showing good stability in a volatile industry.

  • Brian Wong, M.D., Ph.D.: President and Chief Executive Officer, appointed in August 2015. His total yearly compensation for the 2025 fiscal year is approximately $6.98 million.
  • Rodney Young: Chief Financial Officer.
  • Dirk Brockstedt, Ph.D.: Chief Scientific Officer, bringing over 20 years of experience in discovery.
  • William Ho, M.D., Ph.D.: Chief Medical Officer, leading clinical development since 2015.
  • Gwen Carscadden: Chief Human Resources Officer.

The board of directors also saw key additions in June 2025, appointing industry veterans Scott Braunstein, M.D., and Ashley Dombkowski, Ph.D., to provide guidance as the company advances its late-stage clinical programs. Their expertise will help the company navigate the complex path toward potential commercialization.

RAPT Therapeutics, Inc. (RAPT) Mission and Values

RAPT Therapeutics' mission is fundamentally about patient impact, not just pipeline development; the company is driven to discover and commercialize novel therapies for people struggling with inflammatory and immunological diseases. This purpose is backed by core values that emphasize ethical science and a collaborative, patient-first approach to drug development.

RAPT Therapeutics' Core Purpose

The company's cultural DNA is rooted in a commitment to scientific discovery in challenging disease areas, which is a significant factor in how they allocate capital. For instance, the focus on advancing their lead programs is clear in their 2025 financials: Research and development expenses for the nine months ended September 30, 2025, totaled $36.4 million, showing a serious commitment to their clinical-stage work.

Official mission statement

The core mission is a clear statement of intent, focused on a specific therapeutic area and stage of development.

  • Discover, develop, and commercialize novel therapies for patients.
  • Focus on individuals living with inflammatory and immunological diseases.
  • Utilize deep, proprietary expertise in immunology to modulate critical immune responses.

Vision statement

The vision extends beyond drug development to the ultimate goal of transforming patient care and improving quality of life. Honestly, this is the real reason a biopharma company exists.

  • Transform the treatment of inflammatory and immunologic diseases.
  • Improve and empower countless lives through intelligently targeted therapeutics.
  • Aspire to be a leader in targeted oral therapies, translating deep biological insights into clinically meaningful treatments.

RAPT Therapeutics' Core Values

The company's values are the operating principles that guide their scientists and executives, from the lab bench to the boardroom. These values are defintely a compass for making tough, high-stakes decisions.

  • We put patients first.
  • We follow a moral compass.
  • We value open communication.
  • We are fearless, nimble and adaptive.
  • We are one team.
  • This is OUR company.

This patient-centric approach is the long-term play that justifies the near-term cash burn; the net loss for the nine months ended September 30, 2025, was $52.4 million, but the October 2025 public offering raised net proceeds of approximately $234.4 million to fuel this mission. You can explore more about the Mission Statement, Vision, & Core Values of RAPT Therapeutics, Inc. (RAPT).

Given Company slogan/tagline

The company uses a powerful statement that succinctly captures their scientific ambition and their ultimate goal for patients.

  • THE SCIENCE TO OVERCOME INFLAMMATORY AND IMMUNOLOGIC DISEASES.

That's a strong, action-oriented message.

RAPT Therapeutics, Inc. (RAPT) How It Works

RAPT Therapeutics, Inc. is a clinical-stage biopharmaceutical company that designs novel therapies by intelligently modulating key drivers of the immune system to treat inflammatory and immunological diseases. The company creates value by advancing its lead drug candidates, like the anti-IgE antibody ozureprubart, through clinical trials and securing strategic partnerships to reach commercialization.

RAPT Therapeutics, Inc.'s Product/Service Portfolio

Product/Service Target Market Key Features
Ozureprubart (RPT904) IgE-driven Allergic Diseases: Food Allergy, Chronic Spontaneous Urticaria (CSU), Asthma Novel, half-life extended anti-IgE monoclonal antibody; Phase 2b initiated for Food Allergy (prestIgE trial) in October 2025; Phase 2 CSU data showed comparable efficacy to omalizumab with less frequent dosing (Q8W and Q12W).
Tivumecirnon (FLX475) Oncology: Advanced Head and Neck Squamous Cell Carcinoma Oral small molecule C-C motif chemokine receptor 4 (CCR4) antagonist; Designed to block regulatory T cell migration into tumors to enhance anti-tumor immunity; In Phase 2 combination trial with Keytruda.

RAPT Therapeutics, Inc.'s Operational Framework

The company's operational framework centers on its proprietary discovery engine, which focuses on identifying and creating highly selective small molecules and biologics that modulate critical immune pathways. This is a crucial step; you can't get to a Phase 2 trial without a solid molecule to start with.

  • Platform Focus: RAPT's core strategy is built around two primary targets: Immunoglobulin E (IgE) for allergic/inflammatory diseases (with ozureprubart) and C-C motif chemokine receptor 4 (CCR4) for oncology (with tivumecirnon).
  • Clinical Development as Value Driver: Since RAPT is pre-revenue (annual revenue of only $1.53 million as of the most recent data), its primary output is clinical data. The positive Phase 2 CSU data for ozureprubart, reported in October 2025, is the most recent significant value-creating event.
  • Strategic Resource Allocation: Following the termination of the zelnecirnon program in late 2024, R&D expenses for the nine months ended September 30, 2025, dropped significantly to $36.4 million from $60.8 million in the same period a year prior, showing a sharp, necessary pivot to focus resources on ozureprubart and other pipeline assets.
  • Partnerships: RAPT leverages partnerships, such as the one with Shanghai Jeyou Pharmaceutical Co., Ltd. (Jeyou), to accelerate development and access the Chinese market for ozureprubart in indications like CSU and asthma.

RAPT Therapeutics, Inc.'s Strategic Advantages

The biggest advantage for a clinical-stage biotech is having the cash to reach the next critical data readout, plus a differentiated product profile. RAPT has both right now.

  • Extended Cash Runway: The company completed a public offering in October 2025, raising approximately $234.4 million in net proceeds. This financing is projected to fund operations to mid-2028, providing a long runway to execute the Phase 2b food allergy trial and planned Phase 3 CSU studies for ozureprubart.
  • Differentiated Dosing Profile: Ozureprubart's Phase 2 CSU data showed comparable efficacy to a market leader (omalizumab) but with a potentially more convenient dosing schedule of every 8 or 12 weeks (Q8W and Q12W), compared to the competitor's every 4 weeks (Q4W). Less frequent injections defintely improve patient compliance.
  • Oral Small Molecule Platform: Tivumecirnon is an oral small molecule for oncology, which offers a convenience advantage over many injectable biologics, potentially expanding its market reach if later-stage trials are successful.

To understand the investor sentiment driving this financing, you should read Exploring RAPT Therapeutics, Inc. (RAPT) Investor Profile: Who's Buying and Why?

RAPT Therapeutics, Inc. (RAPT) How It Makes Money

RAPT Therapeutics, Inc. is a clinical-stage biopharmaceutical company, so it currently makes money not from selling drugs, but through collaboration and licensing agreements with larger pharmaceutical partners and, critically, through raising capital via equity offerings to fund its extensive research and development (R&D) activities. The company's economic value is tied to the potential future commercial success of its drug candidates, like ozureprubart, not current product sales.

RAPT Therapeutics' Revenue Breakdown

You need to be clear that as of November 2025, RAPT Therapeutics has no commercial product revenue. The company's revenue stream is minimal and highly variable, consisting almost entirely of payments recognized from collaboration and license agreements, which are often non-recurring and tied to research milestones. Analyst consensus for the fourth quarter of 2025 revenue is $0.000, reflecting this pre-commercial status.

Revenue Stream % of Total Growth Trend
Collaboration Revenue 100% Variable (Dependent on milestone achievements)
Product Sales 0% N/A (Pre-commercial stage)

The company's actual revenue for the nine months ended September 30, 2025, is negligible, meaning the 100% figure for Collaboration Revenue represents the source of its minimal recognized revenue, not a large dollar amount. To be fair, this is the standard financial profile for a biotech focused on advancing its pipeline through clinical trials.

Business Economics

The economic engine of RAPT is a classic, high-risk, high-reward model focused on developing intellectual property (IP) that can be monetized later through commercialization or a strategic buyout. The entire business hinges on positive clinical data, which acts as a value inflection point.

  • High R&D Burn: The vast majority of capital is funneled into drug discovery and clinical trials. For the nine months ended September 30, 2025, R&D expenses totaled $36.4 million, which is the core operational cost.
  • Financing Dependency: Operations are financed almost exclusively through equity raises. The company completed a public offering in October 2025, raising net proceeds of approximately $234.4 million to extend its cash runway.
  • Pricing Strategy (Future): While no current pricing exists, the future commercial pricing for its lead candidate, ozureprubart, will target specialty markets for inflammatory diseases like chronic spontaneous urticaria (CSU) and food allergy, suggesting a premium, specialty-drug pricing model common for novel biologics and targeted small molecules.
  • Other Income as Cash Buffer: A significant part of the company's non-core income comes from interest earned on its large cash reserves. Other Income for the nine months ended September 30, 2025, was $5.8 million, a 15% increase year-over-year.

This is a cash-intensive model; positive trial results are defintely the only thing that matters right now. You can dive deeper into the market sentiment and major holders by Exploring RAPT Therapeutics, Inc. (RAPT) Investor Profile: Who's Buying and Why?

RAPT Therapeutics' Financial Performance

Looking at the nine months ended September 30, 2025, the financial picture is typical of a company nearing pivotal trials: significant capital is being consumed to reach the next major milestone.

  • Cash Position: As of September 30, 2025, the company held cash, cash equivalents, and marketable securities of $157.3 million.
  • Liquidity Runway: Following the October 2025 public offering, the company projects its cash balance will fund operations to mid-2028, covering the planned initiation of Phase 3 studies for ozureprubart in CSU.
  • Net Loss: The net loss for the nine months ended September 30, 2025, was $52.4 million, a notable improvement from the $76.6 million loss in the same period of 2024, primarily due to a strategic decrease in R&D spending on other candidates.
  • Expense Management: General and Administrative (G&A) expenses for the nine-month period were $21.8 million, a modest increase from the prior year, driven mainly by higher non-cash stock-based compensation and consulting costs.

Here's the quick math: the company is burning capital at a controlled rate, but the recent $234.4 million capital injection is the lifeblood that buys time for the clinical data to materialize.

RAPT Therapeutics, Inc. (RAPT) Market Position & Future Outlook

RAPT Therapeutics is at a critical inflection point in late 2025, pivoting from a major clinical setback to a strengthened balance sheet and a focused pipeline, primarily driven by its lead asset, ozureprubart. The company's future outlook hinges entirely on positive Phase 2b and Phase 3 clinical data for ozureprubart in large inflammatory markets like food allergy and chronic spontaneous urticaria (CSU).

Competitive Landscape

As a clinical-stage company, RAPT Therapeutics currently holds a 0% market share in commercialized therapeutics; its competition is against established, revenue-generating drugs in its target indications. The most direct competition for its lead drug, ozureprubart, is in the IgE-driven disease space, where a few biologics dominate the current standard of care.

Company Market Share, % (Target Indication) Key Advantage
RAPT Therapeutics 0% (Pre-commercial) Oral, small molecule CCR4 antagonist; potential for less frequent dosing (Q8W/Q12W) than current injectables.
Novartis/Genentech (Omalizumab - Xolair) ~50-60% (CSU Biologics Market Est.) Established efficacy, long-term safety profile, and entrenched prescriber base.
Sanofi/Regeneron (Dupilumab - Dupixent) Rapidly growing in Atopic Dermatitis/Asthma; expanding into other IgE-related diseases Broad label expansion across multiple Type 2 inflammatory conditions; strong sales infrastructure.

Opportunities & Challenges

The company's strategic focus on ozureprubart (RPT904) in inflammatory diseases, coupled with a significant capital raise, maps out clear opportunities, but it still faces the enormous hurdle of clinical-stage execution and regulatory approval.

Opportunities Risks
Positive Phase 2 CSU data for ozureprubart, showing comparable efficacy to omalizumab (Xolair) with less frequent dosing (Q8W/Q12W vs. Q4W). Regulatory uncertainty: Phase 2 CSU trial was not a formal non-inferiority study, requiring critical FDA/regulatory meetings to define the registrational pathway.
Strong cash runway to mid-2028, secured by the October 2025 public offering that raised approximately $234.4 million net. Clinical trial failure: Any unexpected safety or efficacy data in the Phase 2b food allergy trial or planned Phase 3 CSU trials would be catastrophic.
Advancing the oncology asset, tivumecirmon (FLX475), with Phase 2 data showing a 15.6% confirmed overall response rate (ORR) in difficult-to-treat head and neck squamous cell carcinoma (HNSCC). Pipeline concentration risk: The company's valuation is heavily dependent on the success of a single asset, ozureprubart, after the discontinuation of zelnecirnon.

Industry Position

RAPT Therapeutics is positioned as a high-risk, high-reward clinical-stage biotech, specializing in small molecule inhibitors that modulate the immune system, specifically targeting C-C motif chemokine receptor 4 (CCR4) and IgE-driven inflammation.

  • Financial Resilience: The company reported a net loss of $52.4 million for the nine months ended September 30, 2025, a significant improvement from the $76.6 million loss in the prior year period, reflecting a strategic reduction in R&D spend following the discontinuation of the previous lead candidate.
  • Clinical Momentum: The clearance from the FDA in September 2025 to start the Phase 2b prestIgE trial for ozureprubart in food allergy is a key milestone, opening up a multi-billion dollar market opportunity.
  • Strategic Pivot: The firm's shift away from the failed zelnecirnon program and its subsequent, successful financing round in October 2025 demonstrate a decisive, albeit forced, strategic pivot. This focus on ozureprubart in inflammatory diseases and tivumecirmon in oncology provides two distinct shots on goal.

To be fair, the company's market capitalization of approximately $730 million as of early November 2025 reflects significant investor belief in the potential of ozureprubart, but this valuation is defintely a bet on future clinical success, not current revenue. You should check out Breaking Down RAPT Therapeutics, Inc. (RAPT) Financial Health: Key Insights for Investors for a deeper dive.

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