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InflaRx (IFRX) investor relations material
InflaRx Guggenheim Securities Emerging Outlook: Biotech Summit 2026 summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Key product updates and differentiation
Izicopan, an oral C5aR antagonist, shows higher bioavailability, faster onset, and lower CYP3A4 inhibition compared to avacopan, suggesting improved safety and efficacy profiles.
No hepatotoxicity observed in approximately 200 patients treated with izicopan, even at high doses, supporting a clean safety profile.
Izicopan’s rapid achievement of steady-state plasma levels allows for lower dosing and potentially better patient outcomes.
The molecule’s lower risk of drug-drug interactions is attributed to significantly reduced CYP3A4 inhibition.
If avacopan is withdrawn from the market, izicopan could quickly capitalize on the opportunity due to its differentiated profile.
Clinical development and trial results
Proof-of-concept studies in hidradenitis suppurativa (HS) and chronic spontaneous urticaria (CSU) showed encouraging efficacy signals, especially in reducing draining tunnels and pain in HS.
Four-week basket study in HS demonstrated responses comparable or superior to other phase II/III HS trials, despite being non-placebo-controlled.
Long-term toxicology data now supports indefinite dosing, enabling progression to phase IIB trials.
Additional PK simulations and regulatory discussions are ongoing to finalize dosing and trial design for the next phase.
Phase IIB study is required before moving to pivotal trials in HS.
Strategic focus and pipeline outlook
HS remains the primary focus, but CSU is also under consideration for further development, especially in severe patient subsets.
Expansion into other autoimmune indications is possible, with future updates expected at the upcoming Capital Markets Day.
Commercial differentiation in HS will rely on biologic-like efficacy, safety, and unique benefits such as draining tunnel reduction.
Regulatory discussions are ongoing to define endpoints that reflect clinical benefits beyond standard HiSCR measures.
Partnerships may be pursued to expand into additional indications, depending on resources.
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