The Ideal Treatment for CIP

Protection from pulmonary fibrosis with tumor suppression

Executive Summary

  • anti-IL-25 monoclonal antibody candidate (LNR125.38) in development for treatment of CIP
  • Unlike other CIP therapeutics, LNR125.38 significantly reduces tumor growth rather than promoting it
  • Implications in all fibrotic and type 2 inflammatory conditions, with active R&D underway for pulmonary fibrosis, non-allergic asthma, atopic dermatitis, COPD, Ulcerative colitis, and others
  • Licensing and partnership opportunities for additional indications
  • Seasoned founding management has successfully launched multiple drugs
Fluorescent IL-25 and receptors in human idiopathic pulmonary fibrosis biopsy

LEAD INDICATION

Checkpoint Inhibitor Induced Pneumonitis and Interstitial Lung Disease

Up to 30% of cancer patients taking immune checkpoint inhibitors (ICls) will develop pneumonitis as a result of this therapy as more combinations and chronic administration becomes the norm.

Over 20% of those with checkpoint inhibitor pneumonitis (CIP) will die from respiratory failure – with an average 1 month progression­ free survival for severe CIP.

LEAD INDICATION

Checkpoint Inhibitor Induced Pneumonitis and Interstitial Lung Disease

Up to 30% of cancer patients taking immune checkpoint inhibitors (ICls) will develop pneumonitis as a result of this therapy as more combinations and chronic administration becomes the norm.

Over 20% of those with checkpoint inhibitor pneumonitis (CIP) will die from respiratory failure – with an average 1 month progression­ free survival for severe CIP.