AFFiRiS is a clinical-stage biopharmaceutical company that pursues the ultimate aim to improve the lives of patients suffering from neurodegenerative diseases by providing disease-modifying specific active immunotherapies (SAIT) based on its proprietary patented AFFITOME® technology.
We strive to deliver much‑needed therapies to patients with debilitating and life‑threatening neurodegenerative diseases, such as Parkinson’s disease, multiple system atrophy (MSA), dementia with Lewy Bodies (DLB), and Huntington’s disease.
We aim to surpass currently available treatments.
RECENT PRESS RELEASES
18 June 2020
The Lancet Neurology publishes positive results of AFFiRiS’ Phase 1 trial with PD01A in Parkinson’s disease patients
9 April 2020
World Parkinson’s Day: AFFiRiS developing PD01 to treat Parkinson’s disease, a major unmet medical need
3 June 2020
Neurobiology of Disease publishes encouraging preclinical results of AFFiRiS’ antibody mAB C6-17 to treat Huntington’s disease
WHERE TO MEET US
28 January 2020
Biomed Event by Invest Securities
23-25 March 2020
11-12 May 2020
The Neuro4D Conference 2020
Specific Active ImmunoTherapy (SAIT)
Adherence to current therapies can be poor due to complex dosing regimens, and the treatment of many neurodegenerative diseases is stillinadequate. Using our unique AFFITOME technology, we are developing Specific Active ImmunoTherapy (SAIT), which stimulates the body to find and fight proteins central to the development and progression of neurodegenerative diseases. SAIT induces a long‑lasting target-specific immune response, which may be generated by far less frequent dosing regimens (e.g. once or twice a year)
SAIT is an exciting prospect.
We focus on identifying proteins that are involved in the development and progression of neurodegenerative diseases, and establishing novel SAIT treatments against pathogenic forms of these proteins using our unique AFFITOME technology. SAIT has successfully demonstrated proof of concept in both preclinical and clinical studies. Our most advanced product candidates are entering Phase II clinical trials.
We are moving forward.