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Exousia Bio

FDA Orphan Drug Designation

EMA COMP Positive Opinion

Engineering Exosomes to Target Tumors.

Exousia Bio advances next-generation exosome-based cancer therapeutics designed to cross biological barriers and target the treatment-resistant cancer stem cells that drive recurrence.

EXO-NG01
Lead candidate, glioblastoma
2 of 2
Orphan designations secured, US & EU
250+
Publications by our founding scientist
SEC CIK 0001492448

Our Pipeline

Targeting Treatment-Resistant Cells.

EXO-NG01 is an engineered exosome designed to deliver shRNA targeting NANOG mRNA into glioblastoma cells. By downregulating NANOG expression, it targets cancer stemness and treatment resistance — with the goal of enhancing tumor sensitivity to temozolomide.

Our science

A Platform, Not a Drug.

Engineered exosomes act as targeted biological delivery vehicles for nucleic acid medicines — shRNA, siRNA, and DNA. Brain-homing peptide engineering is designed to carry that cargo across the blood-brain barrier to difficult-to-treat tumors.

Latest Updates

Regulatory

FDA grants Orphan Drug Designation for malignant glioma

Designation covers shRNA targeting NANONG mRNA. It does not constitute FDA approval.

Europe

EMA COMP issues a positive opinion

A positive opinion from the Committee for Orphan Medicinal Products extends the regulatory frame to the EU.

Access

A framework for physician-initiated expanded access

Exousia Bio is developing a review pathway for compassionate use requests in mlignant glioma.

Company updates, in your inbox.

Regulatory milestones, preclinical progress, and expanded access news for investors, analysts, and treating physicians.

Company updates