
Oncolytic Molecules that Kill Cancer with Direct & Abscopal Tumor Effects
Neoadjuvant Immunotherapy with Durable Responses Approaching Registrational Studies
Our Pipeline is Led by Ruxotemitide, Rapidly Approaching Registrational Studies
Asset
Preclinical
Phase I
Phase II
Phase III
Partner
Ruxotemitide (LTX-315)
Neoadjuvant resectable melanoma
Seeking Partners
LTX-401
Deep-seated solid tumors
Seeking Partners
More Pipeline Assets...
Ruxotemitide (LTX-315)
Neoadjuvant resectable melanoma
Seeking Partners
PreIIIIII
LTX-401
Deep-seated solid tumors
Seeking Partners
PreIIIIII
More Pipeline Assets...
News
Latest Press Releases
Sep 2, 2026
Lytix Biopharma ASA: Mandatory notification of trade by primary insider
Lytix Biopharma ASA: Mandatory notification of trade by primary insider
Read MoreAug 26, 2026
Lytix Biopharma Q2 2026: FDA Feedback Clears Path to Registrational Phase III Trial for Ruxotemitide (LTX-315) in Patients with Resectable High-Risk Melanoma, Marking Defining Milestone
Lytix Biopharma Q2 2026: FDA Feedback Clears Path to Registrational Phase III Trial for Ruxotemitide (LTX-315) in Patients with Resectable High-Risk Melanoma, Marking Defining Milestone
Read MoreAug 26, 2026
FDA Feedback Clears Path to Registrational Phase III Trial for Ruxotemitide (LTX-315) in Patients with Resectable High-Risk Melanoma
FDA Feedback Clears Path to Registrational Phase III Trial for Ruxotemitide (LTX-315) in Patients with Resectable High-Risk Melanoma
Read More




