The Prophage Series cancer vaccines extend across multiple tumor types. With every insight gained in every clinical trial, we're getting closer to fulfilling our promise to our patients. Current efforts are aimed at exploring new partners globally.
G-100 Newly Diagnosed
- Exciting early results using Prophage G-100 Series in combination with an
approved therapy, Temodar®, in newly diagnosed patients have
led to expansion of the Phase 2 study
G-200 Recurrent
- Promising monotherapy results
in recurrent disease sparked
additional studies
- Immune response demonstrated
R-100 Adjuvant (Oncophage)
- International Phase 3 study completed. Statistically significant
results in patients with better prognostic factors
- Approved in Russia for patients at intermediate risk for disease recurrence
- Phase 2 clinical study ongoing to evaluate immune response.
Data could support additional international regulatory approvals
R-200 Metastatic
- Promising efficacy signals
observed in Phase 2 studies
- Planning Phase 2 combination
study with an approved therapy
NP-150 Pediatric
- Encouraging results in adult glioma have spurred research in pediatric brain tumors
- Manufacturing feasibility of Prophage NP-150 from pediatric brain tumors has been demonstrated
- Phase 1 study to be initiated in newly diagnosed and recurrent setting
M-100 Adjuvant
- New approaches for making the Prophage Series
available from small tumors, typical
of the adjuvant setting, are in the
research phase
M-200 Metastatic
- Immune response demonstrated in Phase 2 studies
- International Phase 3 study completed using Prophage M-200 as
monotherapy. Statistically significant results in patients
with better prognostic factors (eg, stages M1a and M1b)
- Preparing combination studies with immunomodulatory agents