Pipeline

Telomelysin (OBP-301)

The lifecycle commercialization program of Telomelysin employs a considered expansion strategy

lifecycle

 

Potential 2021 launch in esophageal cancer given significant unmet needs

High Mortality
Rates
90%
90% of patients diagnosed with esophageal cancer will die within 2 years
Limited
improvements
Non-operative Settings
Advanced disease at presentation is managed with non-operative approaches (SOC: cisplatin, 5-FU, and radiotherapy alone) which have not seen improvement in outcome for 25 years
Limited
Options
Metastatic Setting
Metastatic esophageal cancer and GEJ cancer have limited approved treatment options and modest efficacy (Nivo and pembro, range of 10-15% in the 3L setting)
Patient
Population
High Potential
Pembrolizumab-refractory: With pembrolizumab’s recent approval in third-line setting, there will be many eligible patients refractory to pembrolizumab that will need another option Older population: Low awareness in elderly allows a huge potential to demonstrate improved outcomes in the older population
FDA
Designations
Opportunity
To pursue Orphan Drug Designation and Breakthrough Therapy Designation

 
 

Given the unmet need in esophageal cancer, Telomelysin has opportunities across different patient types - and in combo with different modalities

combos

 

Telomelysin Platform

molecule

 

Outline / Target indication / Current status

Preclinical studies and proof of concept