Onco Sciences

Precision Oncology at the Molecular Level

Mojo BioPharma's Onco Sciences division is advancing sirexatamab and antisense mRNA technologies to target cancers with unmet medical needs — striking at the genetic roots of malignancy.

Our Oncology Approach

Cancer is fundamentally a disease of dysregulated gene expression. Our Onco Sciences division combines two powerful modalities — antibody-based therapy with sirexatamab and antisense mRNA technology — to target oncogenic drivers with precision that conventional chemotherapy cannot achieve.

Sirexatamab represents a next-generation therapeutic antibody targeting a validated oncology pathway. Our antisense mRNA platform enables selective silencing of cancer-driving genes, offering a programmable approach to oncology that can be rapidly adapted to emerging resistance mechanisms and new tumor targets.

Phase I
Sirexatamab clinical development stage
2
Distinct therapeutic modalities in our oncology platform
Solid + Heme
Tumor types targeted across our pipeline

Pipeline

Onco Sciences Programs

Sirexatamab
Therapeutic Antibody — Solid Tumors
Phase I
Solid Tumors

Sirexatamab is our lead oncology asset, a therapeutic antibody currently in Phase I clinical development for solid tumors. The program targets a validated oncogenic pathway with a differentiated mechanism of action, designed to overcome resistance mechanisms that limit existing therapies.

  • Phase I clinical stage
  • Solid tumor indication
  • Differentiated mechanism of action
  • Resistance-overcoming design
MBP-AS1
Antisense mRNA Platform — Hematologic Malignancies
Preclinical
Hematologic Malignancies

MBP-AS1 leverages our proprietary antisense mRNA technology to selectively silence oncogenic drivers in hematologic cancers. The platform's programmability enables rapid target adaptation and combination potential with existing standard-of-care regimens.

  • Antisense mRNA modality
  • Hematologic malignancy focus
  • Programmable target selection
  • Combination therapy potential

The Antisense mRNA Platform

Antisense mRNA technology works by designing short oligonucleotide sequences complementary to target messenger RNA transcripts. When these antisense sequences bind their targets, they trigger degradation or block translation — effectively silencing the oncogenic gene. Our platform incorporates proprietary chemical modifications that enhance stability, cellular uptake, and target specificity while minimizing off-target effects.

Programmability
Rapidly design sequences against any validated mRNA target
Selectivity
Precise targeting reduces systemic toxicity vs. chemotherapy
Combination Potential
Orthogonal mechanism enables synergy with existing therapies
Resistance Adaptation
Platform can be re-programmed to address emerging resistance

Interested in Our Oncology Program?

Contact our team to learn more about partnership and investment opportunities in Onco Sciences.