Tag Archives: entrepreneurship

Do RESI San Diego and BIO Overlap?

12 May

By Sougato Das, President and COO, LSN

Sougato-Das

The fourth week of June is one of the largest gatherings of life science business development and investment professionals on the calendar, second only to JPM. If you are an early-stage company raising anywhere from $250K to $75M, that week in San Diego is not optional. The question most founders are asking right now is whether attending RESI means missing BIO.

The short answer is no. Here is why.
RESI partnering starts early morning on June 22. BIO Convention partnering does not start until early afternoon. That means you can run a full morning of investor meetings at RESI before BIO gets going. The two venues are about 15 minutes apart, making it straightforward to move between them in the afternoon. RESI has virtual days both that week and the following week, so any meetings that do not fit in person can be held on Zoom with no schedule conflicts.

If you find yourself double booked across both events on Monday afternoon, the partnering systems give you real options. Move the Convention meeting to another day. Move the RESI meeting to the morning or to a virtual slot. Or simply decide which meeting matters more for your specific raise. Having choices is better than not having them.

Fundraising is a numbers game. Companies with tight budgets need to maximize every hour and dollar spent in San Diego each week. RESI is not a scheduling conflict. It is more meetings with investors and pharma external innovation teams that are specifically focused on early-stage deals. Add it to your agenda.

Bonus: Increase your networking ROI by attending the many side events and receptions during Convention week. Luckily we’ve assembled the most complete list for you! Click here.

Register for RESI San Diego

From Story to Outcome: Exit Risk 

12 May

By Dennis Ford, Founder & CEO, Life Science Nation (LSN)

DF-News-09142022

As part of Life Science Nation’s series on converting scientific innovation into investable signal, the final layer of the De-Risk Stack addresses exit risk. (Explore the full series here) After market, technical, regulatory, execution, economic, and financing risks are reduced, the final question becomes clear: how does this become a return?

Exit Risk

From Story to Outcome

At the top of the stack is the question every investor ultimately asks: how does this become a return?

Exit risk is not about predicting a specific transaction. It is about defining a realistic, evidence-based path to liquidity. Without that, even well-executed companies remain difficult to fund across multiple rounds.

This begins with clarity on the most likely exit path, acquisition, licensing, or public markets, aligned with the type of company you are building and the norms of your sector.

From there, you must be able to name a credible buyer universe: specific pharmaceutical, biotechnology, device, or platform companies for whom your asset would represent strategic value. Strategic fit explains why those buyers should care, how your product fills a pipeline gap, extends an existing franchise, enables a new modality, or provides differentiated access to a market.

Timing and value inflection points determine when the asset becomes relevant to those buyers. Clinical data, regulatory milestones, partnership signals, and early commercial traction all influence when interest peaks.

Competitive positioning answers why your asset would be selected over alternatives. Deal structure reality grounds expectations in how transactions are done in your space, including licensing terms, milestones, royalties, and acquisition patterns.

Finally, return potential must align with the expectations of the capital investing in the company. A good company is not always a good investment. The scale and timing of the likely outcome must match the risk and capital required to get there.

Exit risk is resolved when the company presents a credible path from development to liquidity, with clear buyers, clear triggers, and realistic structures.

Core Elements of Exit Risk

  • Exit path clarity
  • Buyer universe
  • Strategic fit
  • Timing
  • Value inflection points
  • Competitive positioning
  • Deal structure reality
  • Return potential

Sequence and Progression

These risks do not resolve independently. The order in which they are addressed determines outcome.

Market clarity precedes technical validation. Technical validation precedes regulatory definition. Regulatory definition precedes scaled execution. Execution enables economic validation. Economic validation supports structured financing. Financing makes an eventual exit possible.

When this sequence is followed, uncertainty is reduced efficiently and value compounds. When it is not, capital is consumed without progress and even strong assets can stall.

From Risk to Signal

The purpose of de-risking is to generate signal.

Investors do not fund ideas; they fund signal, coherent, cross-validated evidence that enough uncertainty has been removed to justify action. Each layer of the stack produces a different class of signal: market signal, technical signal, regulatory signal, execution signal, economic signal, financing signal, exit signal. As these accumulate and align, an opportunity becomes not just understandable, but investable.

Fundraising, in this view, is not persuasion. It is the systematic production and communication of signal.

Implications

For founders, progress is defined by the reduction of uncertainty, not by the volume of activity or the length of the roadmap.

For investors, the De-Risk Stack provides a structured framework for evaluation, what is resolved, what remains unresolved, and what must be proven next.

For ecosystems, it highlights the missing infrastructure between innovation and capital: shared standards, de-risking platforms, and operating systems that help assets move through this process more reliably.

From Framework to System

The De-Risk Stack defines how life science companies become investable. Implementation defines how that process is executed.

At the company level, this means shaping opportunities deliberately, targeting specific layers of risk, executing against clear milestones, and running structured fundraising campaigns.

At the ecosystem level, it means building infrastructure that can systematically identify, assess, and advance assets through the stack, so promising technologies do not stall for avoidable reasons.

When applied consistently, the De-Risk Stack becomes more than a framework. It becomes a system for converting scientific innovation into investable opportunity.

Closing

The challenge in life science is not discovery. It is the disciplined conversion of discovery into investable signal.

De-Risking, Signal, and Investability Series:

  1. The Problem Is Not the Science: A Seven-Part Series on De-Risking, Signal, and Investability
  2. Technical Risk – From Belief to Evidence
  3. From Proof to Approval: Regulatory Risk
  4. From Plan to Progress: Execution Risk
  5. From Progress to Viability: Economic Risk
  6. From Viability to Capital: Financing Risk
  7. From Story to Outcome: Exit Risk

Hot Investor Mandate: Pre-Seed Focused Impact-Driven Early Stage VC Invests in Neurotech and Deeptech With Focus in USA 

5 May

Anearly-stage venture capital firm based in the United States is focused on backing transformative healthcare technologies. The firm primarily invests at the pre-Seed stage, supporting companies at formation and early product development. The firm deploys capital from a dedicated early-stage fund and partners with both individual and institutional investors aligned with its focus on innovation and long-term value creation. While the firm invests in U.S.-incorporated companies, it actively supports globally distributed teams and engages with founders across multiple regions.  

The firm specializes in health-focused deep technology, with a primary emphasis on neurotechnology and adjacent medical device innovation. The firm invests in companies developing technologies that diagnose, treat, or enhance human health through brain-centered or neurological approaches. Areas of interest include neurotechnology platforms, medical devices, diagnostics, and enabling technologies at the intersection of science, healthcare, and engineering. In addition to its core neurotech focus, the firm also evaluates broader medtech opportunities with the potential to deliver scalable impact across healthcare systems.  

From a company and management team perspective, the firm partners with mission-driven founders who combine technical depth with a patient-centered approach to innovation. The firm prioritizes teams developing differentiated technologies with strong scientific foundations, clear clinical relevance, and the potential for global impact. The firm engages closely with founders from the earliest stages, providing strategic guidance, long-term perspective, and support in building durable, high-impact companies. 

If you are interested in more information about this investor and other investors tracked by LSN, please email salescore@lifesciencenation.com

Hot Investor Mandate: Multi-Family Office Firm Invests in Companies and Aligned Funds in Biotech, Precision Medicine, and Medtech  

5 May

The firm is a multi-family office investment and wealth management platform that combines traditional advisory services with direct investment and co-investment opportunities. The firm allocates capital across both direct company investments and third-party funds, providing exposure to high-growth sectors. The firm operates across Europe and the United States and maintains a flexible investment approach spanning multiple asset classes and stages.  

The firm has an active focus on health technology and life sciences, including precision medicine, biotechnology, and select medical technology opportunities. The firm evaluates both companies and funds across early-stage and growth-stage investments, with an emphasis on scientific and clinical innovation that can drive meaningful long-term impact. Areas of interest include personalized healthcare, advanced therapeutic modalities, and technologies that improve diagnosis, treatment, and patient outcomes.  

From a company and management team perspective, the firm partners with teams demonstrating strong domain expertise, execution capability, and strategic clarity. The firm prioritizes opportunities with robust scientific or technical foundations and credible pathways through development, regulatory processes, and commercialization. The firm invests as a collaborative partner, offering capital alongside strategic insight, co-investment flexibility, and access to a broader network of investors and industry relationships.

If you are interested in more information about this investor and other investors tracked by LSN, please email salescore@lifesciencenation.com

Hot Investor Mandate: Asia-Based Healthcare-Focused VC Invests Broadly in All Life Science Sectors, Actively Making Cross-Border Investments 

5 May

A healthcare-focused venture capital firm with a team grounded in biomedical training and industry experience manages both local currency and USD-denominated funds and invests across early and growth stages. The firm has an established track record of investing in companies across multiple financing rounds and geographies, including Asia, North America, and Europe. The firm maintains a strong conviction in long-term growth opportunities within the global healthcare sector, particularly in cross-border innovation.  

The firm invests broadly across therapeutics, medical devices, diagnostics, healthcare IT, and medical services. Within therapeutics, the firm has invested across a range of indications such as oncology, infectious diseases, and autoimmune disorders, covering multiple modalities including small molecules, biologics, and gene-based therapies. The firm also evaluates device and imaging technologies, as well as opportunities in bioinformatics, research tools, and adjacent areas such as animal health. Therapeutic investments typically begin at preclinical stages, while device investments are often made prior to commercialization.  

From a company and management team perspective, the firm does not impose strict requirements and remains open to partnering with a wide range of teams and opportunities. 

If you are interested in more information about this investor and other investors tracked by LSN, please email salescore@lifesciencenation.com

Hot Investor Mandate: Global Multi-Stage Life Sciences Investor Seeks Therapies Addressing High Unmet Medical Need in North America and Asia

5 May

The firm is a life sciences-focused venture capital firm with a global presence and a track record of investing across private and public markets. The firm manages multiple funds backed by institutional and strategic investors and has built a diversified portfolio of companies, including a meaningful number of seed and incubated ventures. The investment team brings extensive experience across venture investing, biopharmaceutical development, academia, and regulatory environments. The firm operates globally with team members based across key innovation hubs in North America and Asia.  

The firm invests across the life sciences sector, targeting areas of high unmet medical need. The firm is flexible across geographies and development stages, leveraging a cross-functional platform to support value creation from early company formation through later-stage and public market investing.  

From a company and management team perspective, the firm prefers to lead investments and typically takes board representation. The firm plays an active role in supporting portfolio companies through strategic guidance across capital markets, business development, clinical strategy, regulatory planning, and commercialization. The firm seeks to partner with management teams that demonstrate strong capability, commitment, and the ability to advance innovative technologies. 

If you are interested in more information about this investor and other investors tracked by LSN, please email salescore@lifesciencenation.com

Oncovita: A Novel Measles-Based Approach to Unlock Immunotherapy in Solid Tumors 

5 May

By Rahul Shetty, Project Management & BD Associate, LSN

Max-Braht-HeadshotIn oncology, one of the most persistent challenges is not a lack of therapeutic innovation, but a fundamental biological limitation: many tumors remain invisible to the immune system. While immunotherapies such as checkpoint inhibitors have transformed treatment paradigms, a significant proportion of cancers, often referred to as “cold” tumors, fail to respond because they simply are not recognized as threats.

Oncovita, a France-based biotechnology company, is addressing this challenge with a novel approach rooted in engineered measles virotherapy. By leveraging the natural biology of the measles vaccine virus, the company aims to expose tumors to immune attack, effectively converting immunologically silent cancers into targets the body can detect and destroy.

This approach is particularly relevant in pleural mesothelioma, one of the deadliest solid tumors, where survival is often measured in months and treatment options remain extremely limited. Its immunologically silent nature makes it largely invisible to immune surveillance and resistant to existing immunotherapies, leaving patients with few effective options.

At the core of Oncovita’s platform is MVdeltaC, an engineered measles vaccine virus designed for intratumoral administration. Many tumors, including mesothelioma, overexpress CD46 – the receptor used by the measles virus to enter cells, providing a natural mechanism for selective targeting. Once inside the tumor, MVdeltaC triggers immunogenic tumor cell death and immune activation by releasing danger signals and tumor antigens, ultimately priming T cells to recognize and attack cancer. In doing so, it converts “cold” tumors into “hot” ones, enabling both local and systemic immune responses.

The use of measles vaccine as a therapeutic backbone offers several advantages. The live attenuated vaccine has been administered to more than four billion people worldwide, establishing a strong safety profile. It replicates in the cytoplasm without integrating into host DNA and is known to stimulate both innate and adaptive immunity, making it well suited for cancer immunotherapy.

Evidence supporting this approach includes a documented remission in a patient with triple-negative breast cancer treated with a measles-based therapy, along with preclinical data showing complete tumor regressions, long-term survival, and systemic immune activation across multiple aggressive tumor models. MVdeltaC has also demonstrated strong potential in combination with checkpoint inhibitors, further expanding its therapeutic relevance.

Oncovita is advancing MVdeltaC with an initial focus on pleural mesothelioma, supported by FDA & EMA Orphan Drug Designation and a clear regulatory pathway. From there, the company plans to expand into triple-negative breast cancer and additional solid tumors, using a stepwise strategy that builds early clinical validation before scaling into larger markets. This stepwise approach allows the company to generate early clinical proof-of-concept in a high-need population before expanding into broader oncology indications. With approximately 9,000 eligible patients annually across the U.S., Europe, and Japan in its initial indications and a significantly larger addressable market across solid tumors, the long-term opportunity is substantial.

Oncovita’s progress is supported by a multidisciplinary team with expertise spanning virology, immunotherapy, and clinical oncology. The company collaborates with leading institutions and key opinion leaders, including experts from Institut Gustave Roussy and MD Anderson Cancer Center, reinforcing the scientific and clinical foundation of its program.

As immunotherapy continues to evolve, enabling the immune system to recognize cancer may be just as important as enhancing its response. Oncovita’s measles-based virotherapy represents a compelling approach to solving this challenge, offering the potential to expand immunotherapy to patients who currently have limited treatment options.

Learn More & Connect

To learn more about Oncovita, visit: https://www.oncovita.fr/

To connect directly with CEO Stephane Altaba, reach out here: stephane.altaba@oncovita.fr