Sepsis
Sepsis could affect everyone, and ultimately leads to death or a long and painful recovery. It starts with a simple infection — a trauma, a surgery, a bacterial infection — that can rapidly escalate into sepsis. When it happens, patients are transferred to the ICU, where medical teams have the tools to manage organ failure caused by sepsis, but nothing to treat sepsis itself and prevent that failure.
SepsIgnite aims to change that through an integrated theranostic platform: combining a first-in-class drug with an early companion diagnostic and marker.
Sepsis affects everyone, regardless of age or gender. Any infection can escalate to life-threatening sepsis within hours. In countries with intensive care access, 10% of deaths are attributed to sepsis and worldwide, the figure exceeds 20%.
Beyond mortality, sepsis causes extensive cellular damage leading to a prolonged and painful recovery lasting months or years. And when caught in time, there is nothing to give, no approved treatment targets the cascade itself.
Post-sepsis syndrome affects 50% of survivors: memory loss, chronic fatigue, recurring infections and post-traumatic stress — for months or years after discharge. Patients leave the ICU without ever being told they had sepsis.
During an infection, when the body perceives a dangerous situation, it reacts violently. What starts as a localized response progresses to sepsis, and the progression is very rapid, accelerating within a few hours. The mortality rate for sepsis without intensive care is extremely high. Sepsis can escalate further to septic shock or acute respiratory distress, both of which are fatal without intensive care.
Once sepsis has set in (as defined by Sepsis 3.0, Singer), the entire body is affected and at least one organ is failing, requiring organ support in the ICU. In septic shock and acute respiratory distress, multiple organ failures (MOF) are interrelated, requiring complex, multifaceted organ supports.
Currently, diagnosis is primarily clinical. It relies on the healthcare provider's experience, training, and expertise. Laboratory findings are helpful but none are considered a reliable marker of sepsis.
Diagnosis is based on: (i) identification of an infection via clinical presentation and microbiological results; (ii) organ failure; and (iii) a moderate increase in blood lactate, indicative of systemic distress, but not specific.
When started very early, aggressive treatment of the infection and moderate resuscitation can prevent progression to sepsis. After that, intensive care must be initiated very quickly (see The Surviving Sepsis Campaign). It enables survival, but does not stop sepsis. On the contrary, in this artificial state created by humans, sepsis will worsen. The body's response is generalized and dysregulated, and the damage it causes further exacerbates the condition.
There are a few treatments available for SARS-CoV-2-related sepsis, but they are not very effective. In the case of septic shock, low-dose corticosteroids can partially replace the adrenal response. There is currently no medication that can effectively control sepsis. Once the infection has been treated, sepsis in the ICU has only negative consequences — it is either fatal or results in a very painful recovery due to extensive cellular damage, including frequent post-traumatic stress.
References: Bone R. (Chest, 1992); T.I.M.E. (Sepsis Alliance); NEWS2; UK Sepsis Trust; Singer M. et al., Sepsis 3.0; The Surviving Sepsis Campaign.
Most approaches tried to block messenger molecules called cytokines, or other cascades such as coagulation or complement. None focused on oxidation — the most effective enforcement mechanism between cells and pathogens. SepsIgnite takes a radically different path: restore vessel protection first, then address the source.
Our proprietary biomarker signature identifies sepsis onset before clinical signs appear. Point-of-care compatible, lab-integrable. Defined CE & FDA pathway.
Hyperactivated white blood cells (the "archer") release oxidants to fight pathogens — but those same oxidants destroy vessel walls. Selenoprotein-P infusion + ultra-rapid sodium selenite restores vascular integrity first, then addresses the hyperactivated immune cells at the source.
Most approaches tried to block messenger molecules called cytokines, activating immune cells (white blood cells, innate response), or other cascades such as coagulation or complement. None of them succeeded.
They did not focus on oxidation, which remains the most effective enforcement mechanism between cells or between cells and pathogens. In sepsis, hyperactivated white blood cells release oxidants in the fight against pathogens — but those same oxidants destroy vessel walls. SepsIgnite's approach: restore blood vessel protection first, then fight the archer (the hyperactivated white blood cells).
Forceville X., Van Antwerpen P., Preiser J.-C. Antioxidants & Redox Signaling, 2021. — Forceville X., Van Antwerpen P., Annane D., Vincent J.-L. Antioxidants & Redox Signaling, 2022.
Combining diagnosis and treatment allows for personalised care. This is the way forward. The diagnostic creates the treatment indication. The treatment validates the diagnostic. Together: a proprietary care pathway and a defensible commercial moat, protected by foundational patents.
SepsIgnite's approach is grounded in more than 80 years of basic research in atomic and quantum biochemistry, translated through 30 years of pre-clinical and clinical work by the founding team.
Small & large, across 3 leading European centers
In leading biochemical journals, incl. Antioxidants & Redox Signaling 2021 & 2022
Multicenter randomised controlled trial, Meaux / Rennes
US Pat. 11,224,633 · EU prosecution in progress
“Sepsis is a tragedy far more common than people realize. Patients leave the ICU without understanding what happened to them, and spend months recovering from something they were never told they had.
For over 70 years, since the birth of intensive care, we have been managing the consequences of this cascade without treating its cause. Intensive care can halve mortality. But survivors still face the post-sepsis syndrome. The cascade itself remains untouched.
What I found, through 30 years of work grounded in 80 years of fundamental biochemistry, is a radically different path. I am convinced it can transform sepsis: from a syndrome we endure, into a disease we detect early and treat at its source.”
The sepsis therapeutics market is vast, growing, and entirely unserved at the cascade level. Combining diagnosis and treatment allows for personalised care — this is the way forward, and SepsIgnite is positioned to own this category.
Beyond the clinical market, a NATO-identified strategic gap in combat trauma and mass-casualty preparedness extends our reach and unlocks non-dilutive defense funding pathways.
A dedicated and experienced team: business builders, clinician, scientist, pharmacist, marketing and IT. More than 100 years of cumulative experience across Medtech, critical care, biochemistry, and digital infrastructure.
Full Scientific Advisory Board and clinical partner network available on request under NDA.
Patient Advisory Board in construction · Full Advisory Board available under NDA.
SepsIgnite's platform is grounded in 30 years of published research across biochemistry, critical care, and translational medicine.
Full bibliography, clinical data package, and methodology notes are available to qualified investors under NDA.
SepsIgnite is building the clinical solution. These patient organisations are raising awareness, supporting survivors, and driving policy change.
SepsIgnite has no commercial relationship with any of the above organisations. Links are provided for informational purposes only.
We're raising €3.5M to unlock 24 months of value creation. Materials are available under NDA.
Or reach us directly at inquiries@sepsignite.com
SepsIgnite · Confidential · All materials subject to NDA