Next Phase Newsletter

Interview with Victoria Paz, Co-founder and CEO of EYWA Biotech By Caitlin Dolegowski, Marketing Manager, LSN

Victoria Paz

Caitlin Dolegowski

EYWA Biotech is leading the charge in developing psychedelic APIs through cutting-edge synthetic biology techniques. In this interview, Victoria Paz, a key figure at EYWA, shares insights into the company’s mission, their innovative approach to solving mental health treatment challenges, and their experience at the Innovator’s Pitch Challenge during RESI Boston. From their fundraising journey to the impact they envision for the healthcare industry, this conversation sheds light on how EYWA Biotech is pioneering solutions in the biotech space.

About the Company

Caitlin Dolegowski (CD): Can you give us a brief introduction to EYWA Biotech and the problem you’re aiming to solve?
Victoria Paz (VP): Eywa Biotech is focused on using synthetic biology and gene engineering to produce GMP-certified psychedelic APIs like psilocybin, DMT, 5-MeO-DMT, and bufotenin. We aim to solve the challenge of providing a reliable, high-quality, and sustainable supply chain for psychedelic compounds used in research and therapeutic applications. Our goal is to address the mental health crisis by ensuring consistent access to these innovative compounds for conditions such as treatment-resistant depression and PTSD.

CD: What inspired you to start EYWA Biotech, and what differentiates your technology from others in the field?
VP: The inspiration behind Eywa Biotech came from the urgent need for new solutions in mental health treatment. Current production methods for psychedelic compounds are often inefficient and environmentally unsustainable. Eywa’s approach stands out because we use synthetic biology to create scalable microorganisms that produce these compounds in fewer steps, cutting down production time and reducing environmental impact. This enables us to deliver high-purity APIs for research and clinical use at a lower cost.

CD: How do you envision your solution impacting the healthcare industry in the next few years?
VP: We believe that Eywa Biotech’s innovations will play a key role in transforming mental health treatment by providing a reliable supply of high-quality psychedelic compounds. Our technology has the potential to make therapeutic psychedelics more accessible to researchers and healthcare providers, accelerating the development of novel mental health treatments. By doing so, we hope to contribute to a broader acceptance of psychedelics in medicine and support the advancement of personalized treatments for conditions like depression and PTSD.

Fundraising Status

CD: Where are you currently in the fundraising process?
VP: We recently closed our pre-seed round, which has allowed us to build and scale our initial production capabilities. We are now preparing to launch our seed round by the end of next year to support further scaling, commercialization, and the development of new formulations and preclinical trials.

CD: What type of investors are you seeking, and what do you hope to achieve with this round of funding?
VP: We are looking for strategic investors who have a strong understanding of biotechnology, mental health, and pharmaceuticals. Ideally, these investors will bring not only capital but also expertise in scaling biomanufacturing and navigating regulatory landscapes. With this round, we aim to scale our production to an industrial level, expand into new markets, and advance our pipeline of formulations and APIs.

CD: How have potential investors responded to your pitch so far, and what has been the most frequent feedback?
VP: Feedback from investors has been positive, especially regarding our innovative approach to scaling psychedelic API production and our focus on sustainability. The most common feedback has been around ensuring that our go-to-market strategy is well-defined, especially in terms of navigating regulatory challenges and market entry in different regions.

Experience at RESI Boston

CD: How was your experience participating in the Innovator’s Pitch Challenge at RESI Boston?
VP: Participating in the Innovator’s Pitch Challenge at RESI Boston was an invaluable experience. It provided us with a platform to showcase Eywa Biotech’s vision to a diverse panel of investors and industry leaders, allowing us to refine our message and receive valuable feedback.

CD: What was the most valuable aspect of presenting to a dedicated panel of investors at the event?
VP: The most valuable aspect was the insightful questions and constructive feedback from the panel, which helped us better understand the investment priorities of various stakeholders in the biotech space. It also offered a great opportunity to build connections with potential investors who align with our long-term vision.

CD: How did the RESI Boston conference contribute to your overall fundraising journey and networking?
VP: The RESI Boston conference significantly boosted our fundraising journey by allowing us to engage directly with high-quality investors and potential partners. It expanded our network within the biotech and life sciences community, helping us identify potential strategic partners for future collaborations.

CD: Did you find the feedback from investors during the pitch challenge helpful, and if so, how?
VP: Absolutely, the feedback was extremely helpful. It highlighted the importance of clarifying our regulatory strategy and demonstrating market readiness. This has guided us in refining our pitch to better address investors’ concerns about market entry timelines and scalability.

CD: Would you recommend the Innovator’s Pitch Challenge to other early-stage biotech companies, and why?
VP: Yes, I would highly recommend it. The Innovator’s Pitch Challenge provides a unique opportunity to receive direct feedback from experienced investors, gain visibility in the industry, and connect with like-minded entrepreneurs. It’s an ideal platform for any early-stage biotech company looking to validate their business model and accelerate their growth.

Interview with Pratip Chattopadhyay, Founder and CEO of Talon Biomarkers By Caitlin Dolegowski, Marketing Manager, LSN

Pratip Chattopadhyay

Caitlin Dolegowski

In this interview, Pratip Chattopadhyay, Founder and CEO of Talon Biomarkers, shares the journey behind the company’s founding and its mission to improve cancer recurrence predictions through advanced immune cell characterization. As a sponsor at the upcoming RESI Boston, Pratip delves into Talon’s cutting-edge technologies, strategic collaborations, and what excites them about connecting with early-stage companies in the biotech space.

Caitlin Dolegowski (CD): Can you tell us about Talon Biomarkers’ founding story and mission?

Pratip Chattopadhyay (PC): Talon Biomarkers was born from my personal frustration with understanding cancer recurrence risks and a broader need in drug development for precise cell-type markers that predict therapeutic outcomes. My career has been dedicated to developing the technologies that accurately characterize immune cells, and Talon is where we connect these technical capabilities to drug discovery and informed patient treatment decision-making.

CD: What sets Talon Biomarkers apart from other biomarker discovery companies?

PC: At Talon, we believe that every patient sample and clinical trial holds valuable insights—there’s always something to learn, even when outcomes aren’t as expected. We leverage cutting-edge, high-parameter immune monitoring technologies to identify predictors of therapeutic efficacy and disease progression. While we operate as a CRO, what truly sets us apart is our deep scientific commitment. We collaborate closely with our clients’ translational teams, not just delivering data but helping to analyze and interpret it, ensuring every experiment reveals actionable insights.

CD: How do you collaborate with clients on experimental design and data interpretation?

PC: We’ve developed unique, automated approaches to accelerate experimental design and execution, ensuring that our work is robust and impactful. Our process starts with understanding the client’s needs through one-on-one consultations and tailoring our strategies to fit their budget and goals, delivering actionable insights.

CD: Can you discuss your strategic partnership with LASE Innovation and how it enhances your services?

PC: Our partnership with LASE Innovation showcases Talon’s tech development expertise. We help companies validate, demonstrate, and introduce new technologies to the scientific community. LASE, for instance, has an exciting technology that transforms static flow cytometry results into dynamic time-lapse insights on immune responses, pushing the boundaries of traditional immune monitoring.

CD: What types of early-stage companies are you most excited to connect with at RESI Boston?

PC: We’re eager to connect with companies developing drugs that affect the immune system or involve immune responses in disease settings. The immune system often serves as a sentinel for many diseases and drug reactions, and we’re excited to demonstrate how our tools can accelerate discoveries.

CD: What emerging trends do you see in immune monitoring and biomarker research?

PC: One major trend is the simultaneous measurement of multiple immune cell parameters, maximizing insights from valuable patient samples. Another is the advancement in complex data analysis. As thought leaders, we guide our clients toward the best biomarker discovery approaches that yield actionable insights.

CD: How can interested companies best engage with Talon Biomarkers during and after RESI Boston?

PC: We’d love to meet you at Table 20, and don’t miss our Wednesday afternoon workshop at 2PM on the third floor of the Westin, St George Room D! If you can’t attend RESI, you can schedule a one-on-one meeting through our website. We look forward to connecting!

Interview with Scott Kozak, Vice President of Research & Development, with contributions from Dr. Angela Lek, Vice President of Research at Muscular Dystrophy Association (MDA) By Caitlin Dolegowski, Marketing Manager, LSN

Scott Kozak

Dr. Angela Lek

Caitlin Dolegowski

I had the opportunity to interview Scott Kozak, Vice President of Research & Development, with contributions from Dr. Angela Lek, Vice President of Research, both at the Muscular Dystrophy Association (MDA), a title sponsor at upcoming RESI Boston. As leading figures in MDA’s mission to advance treatments and find cures for neuromuscular diseases, Scott and Angela bring a wealth of experience and a shared dedication to improving patient outcomes. In this interview, they discuss their professional backgrounds, the latest advancements in research, and offer valuable advice for early-stage companies in the field of Duchenne muscular dystrophy (DMD) research.

Caitlin Dolegowski (CD): Scott, can you share a bit about your background and what led you to your current role as Vice President of Research & Development at the Muscular Dystrophy Association?

MDA: Sure. I have been in the pharmaceutical industry for 35 years. Most of that time has been concentrated on licensing & business/corporate development. I have held senior positions in Big Pharma & Specialty Pharma before concentrating on the entrepreneurial route, co-founding 3 companies along with my own consulting company. As an Entrepreneur In Residence for Yale Ventures, The University of Connecticut Center for Entrepreneurial Innovation, and Connecticut Innovations, I have helped many start-ups with business plans and fundraising as well as helping university faculty & students start companies. My role at MDA was a perfect fit for the experience I have gained throughout my years in the industry. I support the Research areas from a business perspective, which covers strategy, negotiation and other partnering activities for MDA Grants, Venture Philanthropy, MOVR, our patient registry of Real-World Data (RWE), and KickStart, a program encompassing MDA in-licensing IP and partnering for the development of therapeutics for the first time.

CD: What advice would you give to early-stage companies looking to access grants for DMD research, and what resources or programs does MDA offer to support them in this process?

MDA: Advice: It is never too early to reach out to MDA’s research team to initiate conversations about your drug or device development plans. We can provide disease-specific insights, patient perspectives, guidance on trial design as well as help connect you with the right experts in the field. We also highly recommend engaging with TREAT-NMD’s Advisory Committee for Therapeutics (TACT) to receive a comprehensive review on your drug development plans by a multidisciplinary team of experts in the neuromuscular disease space: https://www.treat-nmd.org/what-we-do/tact/

Resources/programs: MDA Venture Philanthropy (MVP) awards early-stage companies with promising therapies in development to treat neuromuscular conditions: https://www.mda.org/science/mda-venture-philanthropy

CD: As we explore innovative approaches in DMD treatment, can you explain the significance of Myosana’s non-viral delivery platform and how it differs from current viral delivery methods?

MDA: Myosana’s non-viral platform differs from AAV-based delivery methods because the therapeutic transgene is not packaged in an existing biological delivery vehicle. Instead, the platform includes proprietary components to deliver DNA that is stable in circulation and can assist in movement from blood vessels to muscle by targeting the GLUT4 transporter that is enriched in skeletal and cardiac muscles. The GLUT4 transporter naturally undergoes trafficking from internal stores to the muscle surface and then back again. The Myosana platform is designed to hitch a ride on GLUT4, leading to internalization of the cargo. Once inside the cell, the DNA cargo is optimized for nuclear targeting and expression.

Myosana’s non-viral delivery platform to deliver full-length dystrophin is mutation agnostic and is anticipated to benefit the entire DMD patient population. In addition, the technology overcomes known hurdles associated with current viral delivery methods utilized in gene therapy such as adeno-associated viruses (AAV) by: 1) not limiting gene size; 2) potential for repeat dosing due to lack of immune response; 3) enriched cardiac and skeletal muscle targeting via the GLUT4 receptor; 4) a predicted decreased cost of goods and better scalability.

CD: What are the potential advantages of delivering the full-length dystrophin gene compared to current microdystrophin approaches?

MDA: Full-length gene delivery of dystrophin at sufficient doses is anticipated to restore full functionality of the dystrophin protein at the sarcolemma, thus achieving a better result than current microdystrophin gene replacement therapy developed for DMD. Microdystrophin gene constructs currently in clinical development are approximately a third the size of full-length dystrophin and can at best achieve a milder Becker Muscular Dystrophy phenotype.

CD: How might Myosana’s technology address some of the limitations of existing gene therapies for DMD, such as gene size restrictions and the inability to repeat doses?

MDA: Currently, patients who test positive for pre-existing AAV antibodies are currently not eligible to receive AAV-based therapies due to immune-related safety concerns. This also precludes patients from being able to receive AAV-based therapies more than once. Myosana’s non-immunogenic platform is not anticipated to exclude any patients based on pre-existing immune concerns. Importantly, current gene therapy technologies are not optimized for durability, hence the ability to re-dose presents a very attractive option for Myosana’s platform.

Myosana’s non-viral delivery platform can be adapted to deliver gene cargoes without the size limitation of AAV. This opens doors for gene replacement therapy across a range of NMDs with genes that exceed the size limit for AAV packaging (e.g. Titin, Nebulin, LAMA2, Dysferlin, RYR1). The lack of size limitation also makes fine-tuning regulation of the transgene expression theoretically feasible by allowing for the use of native promoters and or additional regulatory elements.

CD: Could you elaborate on the mutation-agnostic nature of this approach and its potential to benefit the entire DMD patient population?

MDA: Despite FDA approval for exon skipping drugs for Duchenne (eteplirsen, golodiresen, casimersen, vitolorsen), there is still significant unmet need for the DMD patient population. These specific drugs target only a subset of patients with mutations in hotspot exons of the DMD gene, excluding those with pathogenic mutations that do not fall in exons 45, 51, 53. The recently approved Elevidys gene replacement therapy delivers a truncated version of the dystrophin gene that aims to achieve a milder Becker-like phenotype in patients. The ability to deliver sufficient quantities of full-length dystrophin may be necessary for the maximum achievable benefit and should be helpful to all DMD/BMD patients regardless of their disease-causing mutation.

CD: How does MDA’s support for Myosana’s research align with the organization’s history of funding DMD research, dating back to the identification of the dystrophin gene in 1986?

MDA: MDA has a strong track record in funding DMD research, dating back to the 1980s when we funded Dr. Louis Kunkel who discovered the dystrophin gene as the disease-causing gene responsible for DMD. Over the years, MDA has funded a range of DMD projects ranging from basic science research to clinical trials. Importantly, MDA supported Dr. Jeffrey Chamberlain and his research into understanding the function of dystrophin and whose pivotal findings have enabled the identification of the most functionally important regions of dystrophin. This vital knowledge has enabled the generation of miniaturized dystrophin gene therapies pursued by several companies. MDA also funded Dr. Jerry Mendell who conducted early AAV-based gene therapy trials and pioneered systemic delivery for muscular dystrophies. We continue to support cutting edge therapy development, identifying new technologies that can fill an unmet need in DMD. Myosana was selected for investment via our MVP program committee because their platform represents an alternative option to viral-based gene therapies and potentially holds tremendous therapeutic benefit through the restoration of the full-length dystrophin gene.

CD: What are your expectations for the development of genetic treatment options for DMD patients in the coming years?

MDA: Our expectation for genetic treatment options is to ensure that every patient is eligible for treatment that can restore dystrophin to therapeutic levels that is sustained over many years, thus allowing patients to life longer and more independent lives.

Interview with Dr. Sharon Hesterlee, Executive Vice President and Chief Research Officer at Muscular Dystrophy Association (MDA) By Caitlin Dolegowski, Marketing Manager, LSN

Dr. Sharon Hesterlee

Caitlin Dolegowski

Today, we are excited to feature Dr. Sharon Hesterlee, Executive Vice President and Chief Research Officer at the Muscular Dystrophy Association (MDA), a title sponsor at our upcoming RESI Boston conference. Dr. Hesterlee plays a vital role in advancing research and treatment for neuromuscular diseases. In this interview, she discusses MDA’s investment programs, including the MOVR Data Hub and Venture Philanthropy, and shares insights on supporting biotech startups, key criteria for funding ultra-rare disease therapies, and emerging trends in research. Join us as Dr. Hesterlee offers valuable advice for entrepreneurs seeking to make an impact in the neuromuscular disease landscape.

Interview with Meritxell Teixidó, PhD, CEO & CSO, Gate2Brain By Caitlin Dolegowski, Marketing Manager, LSN

Meritxell Teixidó

Caitlin Dolegowski

Meritxell Teixidó holds a PhD in Organic Chemistry from the University of Barcelona (UB) and an eMBA in Entrepreneurship, Innovation and International Business from UOC. At a scientific level, her field is the synthesis of peptides and the discovery of peptides capable of crossing biological barriers and she was responsible for this research line at the IRB Barcelona during more than 15 years, where she co-directed 10 doctoral theses, published more than 50 articles and participated in 9 patents.

After dedicating more than 15 years to biomedical research at IRB Barcelona, trying to improve the arrival of drugs to the brain by crossing the blood-brain barrier that protects it. She decided to jump more barriers and be the CEO/CSO of Gate2Brain SL. in order to bring technology closer to patients, a challenge and an honor. Jumping barriers is perhaps the common thread that describes her, combining science and innovation with a new vision on leadership, for which she received the Spanish Woman Startup Award 2022 – Inspiration.

Caitlin Dolegowski (CD): Please introduce Gate2Brain and the company’s technology.

Meritxell Teixidó (MT): Gate2Brain is a biotech company focused on the development of therapeutics that efficiently cross biological barriers such as the blood-brain barrier using a radically innovative peptide-based patented technology platform.

G2B-002, the first therapeutic proof of concept of our technology platform, is aimed mainly at the treatment of rare pediatric solid tumors.

CD: Meritxell, you were joined by your colleague, Carles Taulé, Gate2Brain’s Business Development Manager, at RESI Europe and Gate2Brain boasts three women founders. Tell us more about your team.

MT: Gate2Brain has a multidisciplinary team that ranges from peptide scientists to oncologist, from business development to operations. A team that is based in Barcelona and Madrid in Spain but also has key members in Tel Aviv and Mumbai.

CD: What were your experiences at the conference? What worked well for both you and Carles at RESI Europe?

MT: The conference was a great opportunity to share the journey of Gate2Brain and interact with novel potential investors that could help us advance to the clinics.

CD: What stage of fundraising is Gate2Brain in and what are your goals for the rest of 2024 and looking into 2025?

MT: We are fundraising 5M€ to perform the preclinical regulatory studies of G2B-002 (IND enabling studies) and prepare the Clinical Batch of G2B-002.

CD: Congratulations on your first-place finish at RESI Europe’s Innovator’s Pitch Challenge (IPC)! There were over 40 companies in the IPC. What do you think was the key to your success and standing out at RESI Europe?

MT: On one hand, the impact that our technology could have on the first indication that will benefit from it, pediatric brain tumors that have no cure to date. On the other hand, the potential to use our delivery platform to improve the transport of many other drug candidates for brain diseases that are not able to cross the BBB unaided. Our Intelectual property portafolio and the team behind the scenes are to hallmarks that positionates Gate2Brain.

CD: What advice would you like to give to fellow entrepreneurs about RESI conferences?

MT: RESI is the perfect arena to establish connections and network with investors that are aligned with early drug development.

Interview with Sunil Shah, CEO of o2h Ventures | Co-founder @ o2h Group By Claire Jeong, Chief Conference Officer, VP of Investor Research, Asia BD, LSN

Sunil Shah

Claire Jeong

Sunil Shah is a dedicated entrepreneur with over two decades of experience in fostering early-stage biotech innovation. He has focused on building the biotech ecosystem to support fledgling biotech innovations through investment, mentoring, and network building. As Co-founder of the o2h Group and CEO of o2h Ventures, he has led initiatives like the Kickstarter competition and ChaiTime webinars, supporting global biotech startups with integrated drug discovery services and virtual networking. Sunil’s efforts have impacted over ten early-stage companies across five countries and facilitated successful fundraising for o2h Ventures portfolio companies through ChaiTime Portfolio Pitch Day to leverage o2h’s syndicate investor network.

Outside of work, he enjoys biking, running, and competing in Ironman events.

Claire Jeong (CJ): Can you please describe your history in the life science arena?

Sunil Shah (SS): I am a biochemist by training, and I have subsequently spent most of my life in the life sciences arena. Started my career in the life sciences team at PA Consulting gaining early experience working with large Pharma and eventually co-founding a discovery services business that was later sold for a significant multiple. Building on this success we started o2h Discovery to continue to support biotech companies with chemistry and biology, o2h CoWork Labs to provide the biotech companies with the space that they need to start up and o2h Ventures to provide seed capital to biotech companies helping them accelerate their growth journey. I started all these businesses along with my brother Prashant Shah.

I love working with such exciting start-ups and struggle to say ‘no’ when they need support, hence I get involved in every working aspect of a biotech company from finance, business, and strategy and when we are really desperate for science! I am currently either Chair or Non-Executive Director in over ten biotechnology companies at various stages from Preclinical to Phase II and am serving second terms on the Board of Cambridge Angels and the British Biotech Industry Association (BIA).

I am proud to have been recognized by the OBN with a ‘Special Recognition Award’; CEO of the year by the Cambridge Independent Science and Technology Awards and UKBAA Angel of the Year, all in the last five years.

CJ: Can you tell me about how you started your family office, o2h Incubator, o2h CRO, and your o2h venture fund?

SS: Well, I was quite poor after my first start-up (I had a .com and saw the boom-and-bust cycle), I was working as a part-time business development director for a biotech start-up in Cambridge, UK. This was in 2003 and the chemists at CBT were complaining about outsourcing chemistry and we thought there is a market that exists, we just need to do it better. So, we started Oxygen Healthcare in India, with 2 FTEs from Amicus Therapeutics… It was a long slog after that but that was the beginning of the journey. We had already started angel investing in the biotech sector in 2005 with Acacia being one of our first. Through the ‘lens’ of a discovery service provider we were able to speak to big pharma and find out what technologies they were interested in investing in and at the same time connect this to many of the fledgling biotech companies that we were supporting.

The angel investment turned into a Pre-Seed fund ‘o2h Ventures’ and we built our own ‘flywheel’ where we could incubate and mentor start-ups from our own incubator that we bought and developed in Cambridge, UK ‘o2h CoWork Labs’ and we had discovery support on tap as ‘o2h Discovery’ in India/UK continued to flourish. We have made pre-seed investments into 35 biotech companies, mostly over the last 5 years.

CJ: What is your venture funds investment thesis? How many startup investments have you made?  How many exits?  

SS: The UK has an amazing science base, having worked with biotech companies in the UK and USA I would say the industrial and academic talent base is equivalent, and in fact, the UK punches well above its weight bringing in over 40% of all biotech investments across Europe as geography.  Despite these facts, there is a significant and well-understood valuation gap between the UK and the USA. This is largely due to the quanta of seed capital available.

o2h Ventures has built this ‘flywheel’ to incubate and support early-stage companies, despite being a small $10M fund, we have amazing access to new science through our CRO business, o2h Discovery or many of the other organisations (Milner, Start Codon, Wellcome Trust, Cambridge Angels etc..) or Tech Transfer Offices (Cambridge, Nottingham, Oxford, Dundee, Sussex, Manchester, etc..) that we have already spun companies out from.

o2h Ventures invests from two funds, these are not normal fund structures, as they have been set up as tax efficient for UK taxpayers, under what is known as the ‘Enterprise Investment Scheme’. We have now invested in over 35 companies and already, over $400M of capital has been invested into our portfolio that we have developed. Already some of the earlier angel investments have exited such as Acacia and Privitar and now Small Pharma is the first company from our portfolio to be acquired by NYSE-listed company Cybin.

We now seek to raise a more traditional growth fund under a typical GP/LP structure to co-invest in 10-15 of our best companies.

CJ: Are you mostly UK-centric in your investments?

SS:  We think the UK represents huge value for investors given both the science and technology base that we have here. We know the UK landscape very well having grown up in the biotech sector in the UK and hence we think it makes a lot of sense to focus on UK biotech investments for our next phase.

CJ: Do you have LPs in your fund from other regions or just the UK?

SS: Our Pre-Seed funds have investors which are all HNWIs from the UK.

CJ: What is your international strategy, and how do the North American and APAC markets play in your worldview?

SS: We see the USA market as being ‘the bridge’ at a certain stage in the company’s growth; we always seek to bring in US directors onto the boards of our companies which can open the door to US growth capital and potential public market exits. The APAC region represents a massive, fast-growing market with immense potential. While we prioritize the US for now, APAC remains on our radar.

CJ: You have attended and participated in many RESI events over the years. What do you see as valuable to you?

SS: I have been attending the RESI Conference since the very early days, I can’t even remember how many but I go back several years. I always thought that it was amazing that I could meet early-stage companies and other investors who were ALL interested in early-stage biotech companies. No one at a RESI Conference is going to tell you that we don’t work with or do early stage! That’s what really appealed to me. The streams, panels and therapeutic focus areas are so tailor-made for people like me, which is why I love going to the conference and am always willing to support Dennis and his team in expanding his presence or appearing on a panel where possible.

Interview with Silvia Raga Founder and CEO of DyCare By Caitlin Dolegowski, Marketing Manager, LSN

This interview features Silvia Raga of DyCare discussing ReHub, their innovative telerehabilitation platform. Raga explains how ReHub uses advanced technology to enable remote physical therapy, making rehabilitation more accessible and efficient. She highlights DyCare’s recent success at RESI Europe’s Innovator’s Pitch Challenge, attributing it to ReHub’s potential to address key issues in digital health. Raga also discusses the unique networking opportunities at RESI Europe, DyCare’s future expansion plans, and offers advice for entrepreneurs attending similar events. The conversation underscores DyCare’s mission to improve lives through technology and their strategic approach to growth and innovation in the digital health sector.

Silvia Raga

Caitlin Dolegowski

Caitlin Dolegowski (CD): DyCare’s mission is to improve lives through science-based technologies. Can you introduce us to ReHub and explain how it’s revolutionizing digital rehabilitation?

Silvia Raga (SR): ReHub is our flagship product, designed as a comprehensive telerehabilitation platform. It leverages advanced camera detection technology to digitize the rehabilitation process, enabling remote therapies. This innovation provides professionals with a powerful tool to monitor patient progress remotely. At the same time, it offers patients the convenience of executing their highly personalized physical therapy from the comfort of their homes. By bridging the gap between clinicians and patients, ReHub is revolutionizing the way rehabilitation is delivered, making it more accessible, efficient, and effective for everyone involved.

CD: Congratulations on your third-place finish at RESI Europe’s Innovator’s Pitch Challenge! What do you think was the key to your success among over 40 competing companies?

SR: We believe the key to our success lies in addressing critical issues within the rapidly growing digital health market. Improving people’s lives is a priority for many, and the rehabilitation market is enormous. We have identified significant pain points such as the burnout of physical therapists and long waiting lists for patients. Our solution, ReHub, directly addresses these challenges by offering an efficient, accessible, and effective way to deliver personalized rehabilitation remotely.

This innovative approach and the high level of adoption to date resonated with the judges, highlighting the impactful potential of our technology.

CD: How did your experience at RESI Europe differ from other conferences you’ve attended? What aspects of the event did you find most valuable?

SR: Our experience at RESI Europe was unique compared to other conferences we’ve attended. The primary difference lies in the event’s focus on investing. Startups attend with the goal of fundraising, and investors are there specifically to scout for promising startups. This clear alignment of objectives made our interactions more targeted and productive. We found the networking opportunities to be incredibly valuable, as they facilitated meaningful connections with potential investors who were genuinely interested in our technology and vision. Additionally, the structured environment of the Innovator’s Pitch Challenge provided us with a platform to showcase our solution directly to a receptive and relevant audience.

CD: Your team is described as multidisciplinary. How did this diverse expertise contribute to your pitch and overall performance at RESI Europe?

SR: Our team’s diverse expertise was crucial to our success at RESI Europe. Our team includes developers, QA and regulatory affairs specialists, product specialists, physical therapists, and sales and marketing experts. This broad range of knowledge and dedication has enabled us to deliver top-notch medical software. As CEO, having such a well-rounded team behind me instills confidence when pitching in front of anyone. Each team member’s unique perspective and skills have contributed to creating a robust and innovative product, which undoubtedly resonated with the judges and investors at the event.

CD: Following your success at RESI Europe, what are DyCare’s goals for the rest of 2024 and looking into 2025, particularly in terms of market expansion and fundraising?

SR: RESI has been a spectacular platform for showcasing our product to new investors. Moving forward, our primary goals for the rest of 2024 and into 2025 are focused on market expansion and fundraising. We are particularly excited about entering new markets such as LATAM and Italy. In these regions, ReHub has already demonstrated its potential to improve processes for hospitals and insurance companies, delivering better care to patients. We aim to build on this success by establishing a stronger presence in these markets and continuing to refine our product based on user feedback. We are seeking further investment to support our expansion and enhance our technology to meet the evolving needs of the rehabilitation sector.

CD: ReHub is already trusted by prestigious hospitals and insurance companies. How did your participation in RESI Europe help in furthering these partnerships or opening new opportunities?

SR: Participating in RESI Europe significantly boosted our efforts to further existing partnerships and explore new opportunities. The event provided us with a valuable platform to present ReHub to a wide audience of investors and industry leaders in Europe, and it also gave us exposure in a new market such as the US. This exposure has not only enhanced our credibility but also opened doors to new potential partnerships with hospitals and insurance companies that were previously out of reach. Additionally, the feedback and interest we received at RESI have helped us to better understand the market needs and refine our approach to meet the demands of prestigious institutions more effectively.

CD: Based on your experience, what advice would you give to fellow entrepreneurs about making the most of events like RESI Europe?

SR: When attending events like RESI Europe, it’s crucial to be proactive and strategic. Set clear goals and pursue them with determination.

Start by doing your homework: research the key people attending the event and reach out to them beforehand to schedule meetings. This preparation can significantly increase your chances of making valuable connections.

Leverage social media to inform your network that you will be attending. Posting about your presence not only boosts your visibility but also lets potential partners and investors know that you are open to discussions.

Seek an active role at the event, whether as a speaker, a participant in a pitch competition, or in another capacity. Active involvement not only enhances your visibility and credibility but also helps maximize your return on investment.

Don’t underestimate the importance of practicing your pitch. Take the time to refine and rehearse it thoroughly. Show how your product solves a problem and demonstrate its value in action.

Lastly, embrace networking opportunities fully. Events like these are prime opportunities to connect with industry peers and decision-makers. Don’t be shy—engage actively to make the most of your time there.