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One2Treat launches groundbreaking treatment-decision approach to clinical research and market access analysis

One2Treat reflects patient priorities in a single comprehensive treatment evaluation, reducing trial sample size and accelerating patient access to new treatments

Brussels, March 26th, 2024One2Treat, a new innovative start-up offering cutting edge digital health solutions, launches with a pioneering approach that addresses two of the most strategic challenges in the biopharma industry today – incorporating multiple outcomes that matter to patients into a single holistic treatment assessment while accelerating the delivery of new treatments to market. This method, refined through years of research and practical applications, not only enables a more patient-centric approach but also leads to consistent (often drastic) reductions in trial design sample sizes and time to market.

In today’s clinical studies, the focus on one or two primary endpoints often leads to underutilization of valuable data and fails to capture the holistic impact of treatments on patients. Moreover, if the primary endpoints are not met, the trial is considered “negative” regardless of any treatment benefits on other endpoints. Even when a trial is successful, many of the potential insights may be ignored. More importantly, the primary endpoints often fail to reflect what matters to patients, for instance in terms of quality of life.

One2Treat offers a revolutionary approach to clinical trial design and analysis, focused on incorporating all key patient-relevant outcomes into the primary analysis. This paradigm shift draws from extensive industry experience and a rigorous methodology – developed and tested across numerous sponsors’ projects within its parent company IDDI.

At the core of One2Treat‘s offering lies a unique blend of statistical methodology, software, and expert clinical insights. One2Treat‘s proprietary software incorporates the groundbreaking Generalized Pairwise Comparisons (GPC) methodology, allowing non-statisticians to leverage sophisticated statistical techniques with ease. This innovative approach enables sponsors to conduct more patient-centric treatment analysis, by including multiple outcomes in a mathematically rigorous assessment and paving the way for treatments that truly align with patient needs.

Marc Buyse, One2Treat Founder, speaking at the launch of One2Treat, underscored the need for a paradigm shift, stating: “Traditional models often neglect critical aspects of patient well-being, such as quality of life, which can significantly influence treatment effectiveness. Therefore, standard primary endpoints only partially capture patients’ concerns. One2Treat addresses this gap by enabling sponsors to listen to patients’ preferences and evaluate treatment effects across multiple dimensions, within a single reliable assessment. Moreover, leveraging a higher percentage of the collected study data allows for a higher statistical significance and/or a reduced sample size.

Sebastien Coppe, CEO of One2Treat, affirms the company’s commitment to revolutionizing clinical research practices, stating: “Advancements in computing power and a growing focus on patient-centricity present an opportunity for transformative change in the industry. One2Treat‘s innovative approach not only enhances trial design and analysis but also facilitates a more transparent and efficient transition from drug development to market access. Leveraging the same rigorous method to analyze data about overall treatment effects enables us to connect the dots between these two critical elements of global healthcare. Indeed, One2Treat’s unique solution provides a comprehensive benefit-risk evaluation of the treatment based on what matters most to patients (e.g., considering both efficacy and safety outcomes within a single assessment)”.

As One2Treat emerges to disrupt the status quo in both clinical research and HTA/market access, its vision transcends traditional stakeholders to include clinicians and patients themselves. Through its dedicated solution, One2Treat aims to empower individuals to voice their treatment preferences and access personalized care tailored to their unique specific needs.

For more information on One2Treat and its paradigm shifting solution, visit the newly launched website at www.one2treat.com and join the movement towards patient-centric healthcare.

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About One2Treat:

One2Treat is a forward-thinking partner for biopharmaceutical companies, dedicated to delivering transformative insights in clinical trial design, analysis, and market access evaluations to support holistic treatment decisions.

Driven by a commitment to patient-centricity, One2Treat leverages modern statistical methodologies and advanced software solutions to integrate multiple specific efficacy and safety outcomes into a single aggregated measure. This approach allows for the estimation of the Net Treatment Benefit based on patients’ preferences, ushering in a new era of personalized healthcare.

One2Treat’s unique solution empowers sponsors to optimize the design of registration trials, resulting in smaller sample sizes and more clinically relevant analyses. This leads to significantly shorter recruitment timelines and improved biopharma R&D productivity. Additionally, One2Treat facilitates market access through comprehensive benefit-risk evaluations and patient-centric analyses, aligning with the evolving landscape of healthcare needs.

As initiatives to incorporate patients’ preferences into treatment development continue to gain momentum, the adoption of One2Treat’s innovative trial designs is poised to become the new gold standard in the industry.

To learn more about how One2Treat is revolutionizing treatment decisions in clinical research and market access, visit: www.one2treat.com.

Bios:

Marc Buyse, Founder

Marc Buyse is a leading figure in clinical research, renowned for founding IDDI and CluePoints. With decades of academic experience, he has spearheaded innovative methodologies for personalized medicine, meta-analysis, and surrogate endpoints. Marc’s expertise in biostatistics has driven advancements in data-driven decision-making, patient-centric trial designs and regulatory submissions.

As the founder of One2Treat, he continues to lead innovation in clinical research methodologies and technologies, focusing on SaaS solutions for trial design and analysis while prioritizing patients’ needs and clinical relevance at the forefront of every discussion and decision.

Sebastien Coppe, CEO

Sebastien Coppe brings extensive experience in clinical trials and artificial intelligence. Over more than a decade at N-SIDE, he played a pivotal role in leading the company’s Life Sciences activities, contributing significantly to its growth from a small start-up to a purpose-driven organization with over 200 employees.

With a deep understanding of the biopharma industry’s challenges and opportunities, Sebastien made the bold decision to join Marc Buyse in his latest venture, aiming to industrialize his paradigm-shifting solution enhancing treatment decisions. Sebastien is driven by a strong conviction in the potential of innovative digital solutions to meet the overall patients’ needs and accelerate clinical research timelines. He is committed to pioneering approaches that prioritize patient-centricity and enhance biopharma productivity.

Our Vision

Through its innovative solution, One2Treat aims to empower individual clinicians and patients to voice their treatment preferences and access personalized care tailored to their unique specific needs.

Our Mission

One2Treat’s mission is to enable a more holistic evaluation of treatment effects by integrating all key patient-relevant outcomes into a single comprehensive assessment of the Net Treatment Benefit.

Our Unique Value Proposition

One2Treat allows for better leveraging of the large amount of patient data collected in clinical trials and real-world evidence. This leads to more clinically meaningful statistical analysis of treatment effects, incorporating all outcomes that matter to patients. As a result, this approach significantly reduces trial sample sizes and expedites innovative treatments to market.