QuantHealth provides an AI-powered Clinical-Simulator platform that helps pharma and biotech companies de-risk and speed up drug development by simulating clinical trials. Its AI engine uses anonymized data from hundreds of millions of patients, biomedical knowledge graphs, and trial data to create a digital twin and digital-drug environment. Clients can run thousands of trial variations to predict how individuals respond, optimizing trial protocols, patient subgroups, and endpoints before real trials, with reported accuracy up to 90% across oncology, immunology, and cardiovascular therapy. The company differentiates through its scale, data integration, and digital-twin approach, starting with pilots and expanding into long-term partnerships with clients ranging from small biotechs to the top pharma companies, aiming to reduce risk, shorten timelines, and speed patient access to therapies.
Company Size
51-200
Company Stage
Series B
Total Funding
$67M
Headquarters
Tel Aviv-Yafo, Israel
Founded
2020
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GC Cell and QuantHealth Collaborate to Optimize Clinical Development of GCC2005. Wednesday, October 07, 2026 GC Cell, a leader in the cell and gene therapy (CGT) sector within the biopharmaceutical industry, and QuantHealth, the global leader in AI-powered clinical trial simulation, have announced a collaboration to bring a simulation-first approach to the design of upcoming clinical trials for GCC2005, GC Cell's investigational CD5-targeted CAR-NK cell therapy for T-cell lymphoma. The collaboration is intended to advance GCC2005's global clinical development strategy and enhance the design of a planned Phase 2 multi-regional clinical trial (MRCT), using simulation to inform key design decisions before a single patient is enrolled. Drug development is a costly and laborious process, costing $2 billion to $3 billion per approved drug and taking more than a decade from early-stage discovery to regulatory approval. Despite that investment, roughly nine out of ten drug candidates that enter clinical trials ultimately fail - a rate that climbs even higher once preclinical attrition is included. For cell and gene therapies in particular, where patient populations are narrow and precedent is limited, the cost of getting a pivotal trial's design wrong is especially acute. Under the agreement, QuantHealth will apply its AI-powered clinical trial simulation platform to predict treatment responses across different patient populations, assess efficacy outcomes, conduct comparative analyses against competing therapies, and evaluate a range of clinical trial scenarios. GC Cell will use these insights to refine key trial design elements, including patient selection criteria and study endpoints, to optimize the Phase 2 design for GCC2005 and reduce uncertainty in its global development program. For a first-in-class therapy like GCC2005, where there is limited precedent to draw on, this allows GC Cell to stress-test multiple Phase 2 scenarios up front and enter the MRCT with a data-informed design rather than one based on assumptions alone. By collaborating with QuantHealth on a simulation-first approach to clinical development, GC Cell can test design assumptions - patient population, endpoints, comparator performance - against predictive models before committing them to protocol, rather than validating those choices only after a trial is underway. "GC Cell is a recognized leader in Korea's life sciences market, and their adoption of a simulation-first approach further demonstrates their leadership and commitment to innovation. We are excited to help them optimize their clinical trial program, bringing more certainty to decisions about where patients are enrolled and where capital is spent," said Orr Inbar, Co-Founder and CEO of QuantHealth. "This partnership also marks an important step in QuantHealth's global expansion - we're proud to have established our presence in Korea with GC Cell and look forward to continuing to expand into key markets worldwide." GCC2005 is an allogeneic CAR-NK cell therapy candidate targeting CD5, being developed as a potential first-in-class treatment for difficult-to-treat T-cell lymphoma, and is one of GC Cell's key clinical-stage pipeline assets. GC Cell has completed Phase 1a enrollment of GCC2005 in patients with difficult-to-treat T-cell lymphoma and is preparing to initiate a Phase 1b study in collaboration with leading clinical research institutions in Korea. Based on the Phase 1b results, GC Cell plans to advance GCC2005 into a Phase 2 MRCT for registration as part of its global development strategy. "With AI-powered simulation capabilities, we expect this collaboration to enable a more rigorous and data-driven global clinical development strategy for GCC2005," said Sung Yong Won, CEO of GC Cell. "We aim to improve the probability of success and development efficiency of our future Phase 2 program and further strengthen the global competitiveness of GCC2005." About GCC2005 GCC2005 is a fourth-generation CAR-NK cell therapy engineered to direct natural killer (NK) cells against CD5, a marker highly expressed in T-cell lymphoma. It is also designed to co-express interleukin-15 (IL-15) to enhance the in vivo persistence of immune cells. Through these features, GCC2005 is being developed as a next-generation therapeutic candidate with the potential to address limitations of existing treatment approaches. About GC Cell With a core focus on cell therapy, GC Cell offers complete bio healthcare solutions from diagnosis to treatment, and the brand's comprehensive value chain spans R&D, manufacturing, commercialization, and distribution. More info: https://gccell.com/ About QuantHealth QuantHealth is the global leader for AI clinical trial simulation, bringing together the industry's most advanced clinical trial simulations portfolio - 600+ trial simulations across 30 diseases with up to 90% prediction accuracy - and the category's largest real-world data set to help life sciences and biotechnology organizations improve the potential of clinical trial successes. QuantHealth solutions use real-world data and predictive modeling to simulate trials at scale, optimize protocols, reduce risk, and accelerate timelines. The company has been a trusted partner for twelve of the top 20 global pharmaceutical companies. Contacts Mia Hinz [email protected]
QuantHealth raises $45 million Series B, led by Qumra Capital, to accelerate simulation-first clinical trial development. Funding will advance QuantHealth's R&D, product innovation, and commercial expansion following 8x sales growth in 2025 TEL AVIV, Israel-(BUSINESS WIRE)-QuantHealth, a global leader in AI-driven clinical trial simulation, today announced a $45 million Series B. The round was led by Qumra Capital, with support from additional investors, including Pitango HealthTech, Sanofi Ventures, Artofin Venture Capital Fund L.P., Bertelsmann Healthcare Investments (BHI), GC Ventures, NewHealth Ventures, Shoni Top Ventures, and Esplanade Ventures. Building on strong momentum and growing adoption of its solutions, QuantHealth will use the new capital to scale its enterprise-wide impact and accelerate adoption of simulation-first clinical development. With this approach, life sciences organizations move away from designing clinical trials based on historical benchmarks and subjective assumptions, and toward launching trials that have been tested, optimized, and de-risked through AI-driven simulation before a patient is enrolled or capital is deployed. Key investments include: * Advancing its R&D capabilities with next-generation AI models, deeper scientific validation, expanded data sets, and increased therapeutic coverage * Growing its workforce to support increasing industry demand and deliver expert-driven client engagements * Expanding its product portfolio across the clinical and commercial lifecycle, from trial design through go-to-market positioning, with a focus on demonstrating measurable impact Clinical trials remain one of the most costly and uncertain phases of drug development, with more than 90% of drugs that enter clinical development ultimately failing, approximately 75% due to efficacy and safety. As pressure mounts to bring therapies to market faster, while still ensuring safety and efficacy, pharmaceutical and biotech companies are increasingly turning to predictive technologies to guide decision-making. "Today, clinical development decisions are still largely made through real-world iteration - running trials, waiting for results, and adjusting at significant cost and risk. We're fundamentally changing that model," said Orr Inbar, CEO and co-founder of QuantHealth. "With our predictive simulations, teams can evaluate clinical and commercial decisions before enrolling a single patient or committing capital. This funding allows us to scale that approach, making simulation a standard step in development and fundamentally improving how drugs are brought to market." To date, QuantHealth has simulated more than 600 clinical trials across 30 indications, achieving up to 90% predictive accuracy. The company plans to expand to more than 40 indications across its core therapeutic focus areas, including oncology, cardiometabolic, and inflammation. "AI has already transformed drug discovery, and clinical trials are the next frontier. It's a market in which hundreds of billions of dollars are spent annually on clinical trials, and one that is ripe for a smarter, more efficient approach," said Reut Yehuda Golan, partner at Qumra Capital. "QuantHealth is at a significant inflection point: their technology is mature, the market is ready for change, and the proof points are already there. At Qumra, we invest in companies that transform industries, and QuantHealth is exactly that, a company on its way to defining and leading a massive category, with groundbreaking technology that is already widely adopted across the world's leading pharmaceutical companies." "As one of QuantHealth's earliest investors, we have had the opportunity to watch the company help define an emerging category at the intersection of AI and clinical development," said Cris De Luca, Partner at Sanofi Ventures. "As the pharmaceutical industry increasingly looks to leverage AI to improve decision-making across the development lifecycle, simulation technologies are becoming an important part of the drug development toolkit. QuantHealth has been an early pioneer in this space, and we look forward to the company's continued growth and impact across the industry." About QuantHealth QuantHealth is the global leader in AI-powered clinical trial simulation. The company combines the industry's most advanced clinical trial simulations portfolio, spanning more than 600 trials and 30 indications, with one of the largest real-world datasets in the category. Its solutions enable pharmaceutical and biotechnology organizations to optimize trial design, reduce risk, and accelerate development timelines. QuantHealth partners with 12 of the world's top 20 pharmaceutical companies to improve clinical success rates and bring better therapies to patients faster. August 4th, 2026 August 3rd, 2026
QuantHealth raises $45M Series B to use AI to predict how patients will respond to therapies. QuantHealth has raised $45 million in Series B funding to scale an ambitious idea: use AI to test clinical trials before drugmakers test them on patients. The round was led by Qumra Capital, with participation from Pitango HealthTech, Sanofi Ventures, Artofin Venture Capital Fund L.P., Bertelsmann Healthcare Investments (BHI), GC Ventures, NewHealth Ventures, Shoni Top Ventures, and Esplanade Ventures. The funding arrives as pharmaceutical companies search for ways to attack one of drug development's most stubborn problems. Clinical trials can consume years and enormous amounts of capital, yet most drugs entering clinical development never reach the market. QuantHealth wants drugmakers to learn more about the likely outcome before committing patients, time, and millions of dollars to a trial. Instead of relying primarily on historical benchmarks and assumptions when designing studies, the Tel Aviv, Israel-based QuantHealth creates AI-powered simulations that let researchers test different trial designs and clinical decisions before patient enrollment begins. Think of it as a computational test run for a clinical trial. That distinction matters. AI has attracted billions of dollars into drug discovery, where companies use machine learning to identify targets, predict molecular behavior, and search for potential drug candidates. QuantHealth is applying AI farther down the drug-development pipeline, at the stage where promising science meets the expensive reality of human clinical testing. With $45M in new funding, Israeli tech startup QuantHealth wants to simulate a clinical trial before the real trial begins. QuantHealth says it has simulated more than 600 clinical trials across 30 indications and has achieved predictive accuracy of up to 90%. The company plans to extend coverage beyond 40 indications, with oncology, cardiometabolic diseases, and inflammation among its main therapeutic areas. QuantHealth says its technology combines clinical trial simulation models with large real-world datasets to predict how different patient populations, endpoints, treatment arms, dosing decisions, and other trial parameters could affect an eventual study. For pharmaceutical companies, the goal isn't to replace clinical trials. It is to make better decisions about which trials to run and how to design them. That distinction is significant. Clinical trials exist to establish whether therapies are safe and effective in real patients, and an AI prediction cannot substitute for that evidence. QuantHealth's bet is that simulation can become an earlier decision layer, helping researchers identify weak trial designs or promising alternatives before millions of dollars have already been committed. "Today, clinical development decisions are still largely made through real-world iteration - running trials, waiting for results, and adjusting at significant cost and risk. We're fundamentally changing that model," said Orr Inbar, CEO and co-founder of QuantHealth. "With our predictive simulations, teams can evaluate clinical and commercial decisions before enrolling a single patient or committing capital. This funding allows us to scale that approach, making simulation a standard step in development and fundamentally improving how drugs are brought to market." A costly problem hiding behind every new drug The economics explain why investors see an opportunity. More than 90% of drugs entering clinical development eventually fail, according to figures cited by QuantHealth, with roughly 75% of those failures tied to efficacy and safety. A failed clinical trial can represent years of research, patient recruitment, regulatory work, manufacturing preparation, and investment. Later-stage failures can be particularly painful since companies have already committed substantial resources by the time a drug reaches larger studies. This creates a compelling use case for predictive software. A simulation doesn't have to predict every outcome perfectly to have economic value. If it can reliably help researchers identify a poorly constructed study, select a better patient population, reconsider an endpoint, or abandon an unlikely program earlier, the savings can become substantial. That is the business case QuantHealth is selling. The company has worked with 12 of the world's top 20 pharmaceutical companies, giving it something many AI drug-development startups still lack: adoption among large drugmakers. From AI drug discovery to AI clinical development. The investment comes amid a broader shift in how the pharmaceutical industry is thinking about artificial intelligence. Much of the first wave of AI investment in biotech centered on discovery. Startups promised to search huge chemical spaces, identify biological targets, design molecules, and shorten the earliest stages of drug development. Clinical development presents a different challenge. A molecule can look promising in a laboratory and still fail once tested across diverse groups of patients. Trial design introduces another set of variables, from eligibility criteria and endpoints to dosing schedules and patient characteristics. QuantHealth is betting those variables can increasingly be modeled before researchers commit to a real-world study. "AI has already transformed drug discovery, and clinical trials are the next frontier. It's a market in which hundreds of billions of dollars are spent annually on clinical trials, and one that is ripe for a smarter, more efficient approach," said Reut Yehuda Golan, partner at Qumra Capital. "QuantHealth is at a significant inflection point: their technology is mature, the market is ready for change, and the proof points are already there. At Qumra, we invest in companies that transform industries, and QuantHealth is exactly that, a company on its way to defining and leading a massive category, with groundbreaking technology that is already widely adopted across the world's leading pharmaceutical companies." The new funding will go partly into research and development, including new AI models, larger datasets, scientific validation, and broader therapeutic coverage. QuantHealth plans to grow its workforce to support pharmaceutical customers and extend its products beyond clinical trial design into other parts of the clinical and commercial drug lifecycle, including go-to-market positioning. That broader strategy could turn the company from a clinical trial simulation vendor into a decision platform spanning several stages of drug development. Sanofi Ventures returns as an investor. The investor list offers another signal about where QuantHealth sits in the pharmaceutical ecosystem. Sanofi Ventures, the venture arm associated with pharmaceutical giant Sanofi, participated in the Series B after backing QuantHealth earlier in its development. "As one of QuantHealth's earliest investors, we have had the opportunity to watch the company help define an emerging category at the intersection of AI and clinical development," said Cris De Luca, Partner at Sanofi Ventures. "As the pharmaceutical industry increasingly looks to leverage AI to improve decision-making across the development lifecycle, simulation technologies are becoming an important part of the drug development toolkit. QuantHealth has been an early pioneer in this space, and we look forward to the company's continued growth and impact across the industry." Strategic investment from the pharmaceutical sector carries a different significance from venture funding alone. Large drugmakers are the customers QuantHealth needs to convince if simulation-first clinical development is going to move from an interesting AI application into standard industry practice. The company says its existing relationships with 12 of the top 20 pharmaceutical companies already give it a foothold. The harder question is whether predictive simulation can become trusted enough to influence high-stakes decisions involving programs worth hundreds of millions of dollars. Why QuantHealth's $45 million raise matters. AI's next major test in pharmaceuticals may have less to do with discovering more molecules and more to do with figuring out which drugs have the best chance of surviving clinical development. That's where QuantHealth is positioning itself. The company isn't promising to eliminate clinical trials or predict human biology with certainty. Its opportunity rests on a more practical proposition: give drug developers better information before they make some of their most expensive decisions. There is still a high bar to clear. Predictive accuracy across hundreds of simulations does not mean every future trial can be forecast with the same precision, and pharmaceutical companies will want extensive validation before allowing AI-generated predictions to influence major clinical programs. Yet the economics create a strong incentive to try. If simulation can expose a flawed trial design before hundreds of patients are recruited, the value isn't simply faster software. It could mean avoiding months or years of work on a study that had a poor chance of succeeding from the start. QuantHealth's $45 million Series B gives the company more capital to prove that case. And if simulation becomes a routine checkpoint before patient enrollment, the biggest change may happen long before anyone enters a clinic: the clinical trial could increasingly begin inside a computer.
QuantHealth raises $45 million Series B to bring AI simulations to the costly world of clinical trials. The Israeli startup says its technology has simulated more than 600 trials and can help drugmakers test decisions before enrolling patients or spending billions on development. 15:12, 04.08.26 QuantHealth, which develops AI-based simulations for clinical trials, has raised $45 million in a Series B funding round led by growth fund Qumra Capital, with participation from additional investors including Pitango HealthTech, Sanofi Ventures, Artofin Venture Capital Fund L.P., Bertelsmann Healthcare Investments (BHI), GC Ventures, NewHealth Ventures, Shoni Top Ventures and Esplanade Ventures. The latest round brings the Israeli company's total funding raised to $75 million. Previous investors include pharmaceutical giant Sanofi and Accenture Ventures, the investment arm of consulting firm Accenture. QuantHealth plans to use the new capital to expand its research and development capabilities, develop next-generation AI models, increase its datasets and broaden its therapeutic coverage. The company also intends to expand its workforce and extend its product offering across the drug development lifecycle, from clinical trial design to commercial planning. The company was founded in 2020 by Orr Inbar, who previously worked at ConcertAI, and Arnon Horev, who previously led business operations at life sciences company Nucleai and managed marketing and sales at medical technology company EarlySense. The company currently employs approximately 85 people in offices in New York and Tel Aviv. Clinical trials remain one of the most expensive and uncertain stages of drug development. More than 90% of drugs that enter clinical development ultimately fail, with approximately 75% of failures attributed to efficacy and safety issues. Faced with rising development costs, increasing competition and pressure to bring new therapies to market faster, pharmaceutical and biotechnology companies are increasingly adopting predictive technologies to improve decision-making. QuantHealth's technology allows pharmaceutical companies to simulate clinical trials before enrolling patients or committing significant capital. Instead of relying primarily on historical benchmarks and subjective assumptions, companies can use AI-driven simulations to test different trial designs, identify risks and optimize decisions before launching real-world studies. "Today, clinical development decisions are still largely made through real-world iteration, running trials, waiting for results, and adjusting at significant cost and risk. We're fundamentally changing that model," said Orr Inbar, CEO and co-founder of QuantHealth. "With our predictive simulations, teams can evaluate clinical and commercial decisions before enrolling a single patient or committing capital." To date, QuantHealth has simulated more than 600 clinical trials across 30 medical indications, achieving predictive accuracy levels of up to 90%, according to the company. It plans to expand coverage to more than 40 indications, focusing on areas including oncology, cardiometabolic diseases and inflammatory diseases. The company says its platform is already used by 12 of the world's top 20 pharmaceutical companies, helping them optimize trial design, reduce risk and improve development timelines.
QuantHealth, an Israeli clinical trial simulation software provider, has raised $45 million in Series B funding, CEO Orr Inbar announced. The company's software helps model and simulate clinical trials. Demand for modelling and simulation software is increasing as AI promises to reduce drug development costs and timelines. The funding will support QuantHealth's expansion in this growing market. The company specialises in providing tools that enable pharmaceutical developers to simulate clinical trial outcomes before conducting actual trials, potentially streamlining the drug development process.