Pipeline
A broad pipeline, one platform
Eleven oncology indications and four infectious-disease programs. Stages shown reflect preclinical and IND-enabling progress; all candidates are investigational.
Oncology
Eleven indications, led by OTM001
Breast cancer (OTM001) is furthest along — through Pre-Clinical and into IND-Enabling.
Breast Cancer
OTM001
Through IND-Enabling
Breast Cancer: through IND-Enabling stage.Liver
Through Pre-Clinical
Liver: through Pre-Clinical stage.Prostate
Through Pre-Clinical
Prostate: through Pre-Clinical stage.Lung Carcinoma
Through Pre-Clinical
Lung Carcinoma: through Pre-Clinical stage.Bladder
Through Pre-Clinical
Bladder: through Pre-Clinical stage.Cervical
Through Pre-Clinical
Cervical: through Pre-Clinical stage.Melanoma
Through Pre-Clinical
Melanoma: through Pre-Clinical stage.B-Cell Leukemia
Through Pre-Clinical
B-Cell Leukemia: through Pre-Clinical stage.Head & Neck
Through Pre-Clinical
Head & Neck: through Pre-Clinical stage.Ovarian
Through Pre-Clinical
Ovarian: through Pre-Clinical stage.Glioblastoma
Through Pre-Clinical
Glioblastoma: through Pre-Clinical stage.
Infectious Disease
Four programs in development
Applying the same precision platform beyond oncology, led by RSV.
RSV
Through Pre-Clinical
RSV: through Pre-Clinical stage.Zika
Through Pre-Clinical
Zika: through Pre-Clinical stage.Ebola
Through Pre-Clinical
Ebola: through Pre-Clinical stage.COVID-19
Through Pre-Clinical
COVID-19: through Pre-Clinical stage.
Lead-program spotlight
First-in-Human study — TNBC
A neoadjuvant, intratumoral (IT) injection of pDNA-LNP for triple-negative breast cancer: a 3-patient study with a Florida-based CRO, initiating Q2 2026.
- Complete
Preclinical & IND-Enabling
Proof-of-concept across 24 cell lines, animal models, tumoroids, and organ-on-a-chip studies.
- Next milestone
First-in-Human (FIH) — Q2 2026
Neoadjuvant intratumoral injection of pDNA-LNP for TNBC. A 3-patient study with a Florida-based CRO.
- Future
Subsequent Clinical Phases
Phased clinical evaluation to follow, contingent on FIH outcomes and regulatory guidance.
Timeline reflects planned First-in-Human timing only. OTM001 is investigational and has not been approved by any regulatory authority.