Belite eyes tinlarebant approval after late-stage Stargardt success
Belite Bio is seeking US approval of its lead ophthalmology asset, tinlarebant, in Stargardt disease 1 (STGD1) following the positive…
Belite Bio is seeking US approval of its lead ophthalmology asset, tinlarebant, in Stargardt disease 1 (STGD1) following the positive…
Sydnexis has revealed further data of its paediatric progressive myopia (PPM) candidate, which met both the primary and secondary endpoints,…
FELIQS has concluded a $9m Series A funding round, a significant step towards advancing the FLQ-101 clinical programme for preventing…
Viridian Therapeutics’ veligrotug has shown one-year durability in a Phase III trial in patients with active thyroid eye disease (TED).…
China-headquartered VivaVision Biotech is looking to advance its non-steroidal therapy, VVN461-CS-201 (VVN461), in a Phase III trial after the candidate…
Outlook Therapeutics’ second attempt to obtain US approval for its wet age-related macular degeneration (wet AMD) therapy, Lytenava (bevacizumab-vikg) has…
Glaukos plans to file for US approval of its iLink corneal cross-linking therapy Epioxa (Epi-on) for treating keratoconus after the…
Viridian Therapeutics’s veligrotug has met all primary and secondary endpoints in a Phase III trial in active thyroid eye disease…
Boehringer Ingelheim and CDR-Life have reported positive outcomes from the Phase I clinical trial of BI 771716, a new treatment…
MSD (Merck & Co) and its wholly-owned subsidiary EyeBio have announced the start of the Phase IIb/III BRUNELLO clinical trial…