https://www.sec.gov/Archives/edgar/data/1636050/000104746919001193/a2238033z424b5.htm
The AXO-AAV-OPMD clinical program is expected to begin in the second half of 2019, and the final design will be informed by discussions with the FDA andother regulators.
from the Axovant prospectus:
Gene Therapy ProgramClinical Indication Development Stage 1 AXO-AAV-GM1
GM1 gangliosidosis Clinical-ready 2 AXO-AAV-GM2
GM2 gangliosidosis (including Tay-Sachs disease and Sandhoff disease)
Clinical
3 AXO-LENTI-PD
Parkinson's disease
Clinical
4 AXO-AAV-OPMD
Oculopharyngeal muscular dystrophy
Preclinical
5 AXO-AAV-ALS
Amyotrophic lateral sclerosis
Research
6 AXO-AAV-FTD
Frontotemporal dementia
Research
7 Four additional AXO-AAV
Undisclosed
Research
8 Collaboration Programs