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INNOVATION, EXPERTISE AND EXPERIENCE
Discovering New Treatments for Rare and Ultra-Rare Diseases
Our Philosophy
At Atlas Molecular Pharma we are “patient-centric” and strongly believe that the key aspect of delivering an effective treatment requires input and support from patients and their families suffering from Rare and Ultra-Rare Diseases.
Our most advanced project is targeting Congential Erythropoietic Porphyria, but we are also in the process of assessing other Rare and Ultra-Rare Diseases for which we believe we can discover a treatment.
Proprietary Platform Technology
Pipeline
Prion Disease: Prion disease (e.g., Creutzfeldt-Jakob disease) results from the progressive accumulation of an abnormal form of the naturally occurring cellular prion protein leading to subsequent adverse effects on brain function and ultimately death. This project is at the hit identification phase of discovery.
Other diseases: We are currently assessing a range of other diseases to initiate further projects which will benefit from a pharmacological chaperone therapeutic.