Preclinical stage · Anti-infectives

Turning the body's own defence into an anti-infective.

Inicure develops patent-protected small molecule FPR1 agonists that activate the innate immune system to treat infectious disease — and to combat the growing threat of resistant bacterial infections.

Diagram of Inicure's FPR1 agonist mechanism activating immune cells to clear bacterial infection
Fig. 1 — Inicure's molecules boost the innate immune system, targeting infections caused by a wide range of pathogens.

The challenge

Antibiotic-resistant infections are becoming a global health threat.

As traditional antibiotics become less effective and common infections increasingly challenging to treat, new approaches are critical. By developing novel anti-infective compounds, Inicure is targeting infectious disease — addressing a global health threat and a substantial, growing market.

23M
Infections analyzed by WHO
1.27M
Lives lost annually to antimicrobial resistance
$100T
Potential economic impact by 2050

Source: WHO global research report on antimicrobial resistance.

The Inicure approach

Potent agonists of the formyl peptide receptor-1 (FPR1).

Rather than attacking bacteria, Inicure harnesses the innate immune system. Our compounds selectively activate FPR1 and stimulate the NOX2 pathway, enhancing the immune system's natural production of reactive oxygen species — critical for bacterial killing and for resolving inflammation.

  1. 01

    Selective FPR1 activation

    Our small molecules act as potent, functionally selective agonists of the formyl peptide receptor-1 (FPR1) on immune cells.

  2. 02

    NOX2 and ROS response

    FPR1 signalling stimulates the NOX2 complex to produce reactive oxygen species (ROS) — a natural mechanism for bacterial killing and inflammation resolution.

  3. 03

    The immune system clears the infection

    Because the compounds do not target bacteria directly, the risk of resistance development is significantly lower.

Neutrophil engulfing a bacteria
Fig. 2 — Neutrophil engulfing a bacteria. AI generated picture.

Supporters

  • Seal of Excellence logo
  • INCATE logo
  • Knut and Alice Wallenberg Foundation logo
  • Potter Clarkson logo

Pipeline

Advancing toward clinical development.

Inicure's lead compounds are in the preclinical stage, moving along a clear trajectory toward first-in-human studies.

FPR1 agonists

  • Discovery

    Completed

    Discovery: Completed
  • Early preclinical

    Ongoing

    Early preclinical: Ongoing
  • Late preclinical

    Not started

    Late preclinical: Not started
  • Phase 1

    Not started

    Phase 1: Not started
    • Phase 2 - Topical use

      Not started

      Phase 2 - Topical use: Not started
    • Phase 2 - Systemic use

      Not started

      Phase 2 - Systemic use: Not started

Why Inicure

A different route to treating infection.

Host-directed, not bacteria-directed

The compounds work through the innate immune system rather than attacking bacteria, significantly lowering the risk of resistance development.

A new mechanism of action

Selective FPR1 agonism driving NOX2-produced ROS is a fundamentally new approach to inhibiting and treating infection and inflammation.

Topical to systemic versatility

Water-solubility and specificity allow applications from infected wounds to severe systemic infections such as urinary tract infections.

Patent-protected assets

Inicure is developing patent-protected compounds, supported by peer-reviewed science and an experienced drug development team.

Preclinical evidence

Efficacy in human cells and preclinical models — without toxicity.

Our compounds have demonstrated efficacy against resistant pathogens including Escherichia coli (UPEC) and Staphylococcus aureus (MRSA). Because they do not directly target bacteria, the risk of resistance development is significantly lower. Early safety studies indicate no adverse toxicological effects.

Lind S, Dahlgren C, Holmdahl R, Olofsson P, Forsman H. Functional selective FPR1 signalling in favour of an activation of the neutrophil superoxide generating NOX2 complex. J Leukoc Biol. 2021; 109: 1105–1120.

Read the publication
Preclinical data figure showing functional selective FPR1 signalling and NOX2 activation
Fig. 3 — FPR1 signalling and the NOX2 complex. Images by BioRender, produced by Dr Heather Chicks, Swansea University.

About Inicure

A Gothenburg spinoff with deep immunology roots.

Inicure AB is a spinoff from the autoimmunity-focused company Pronoxis AB. The company develops anti-infectious assets activating the formyl peptide receptor-1 (FPR1) and was founded in 2024 by Peter Olofsson-Sahl, Sara Malcus, Johan Bylund and GU Ventures AB.

Portrait of Peter Olofsson-Sahl

Peter Olofsson-Sahl

CEO

Preclinical drug development and international project management. Founder of several innovative research companies.

Portrait of Sara Malcus

Sara Malcus

Chair Board of Directors

Business development and investment management, with extensive life science start-up executive and Board experience.

Portrait of Johan Bylund

Johan Bylund

CSO

Professor in Microbiology, focused on immunology and infections including targeting of immunological mechanisms.

Portrait of Felix Sanchez Klose

Felix Sanchez Klose

Researcher — Product Development

Immunology and infection biology combined with bio-engineering, method development and instrumentation.