A First-in-human, Open-label, Single Ascending Dose Study to Assess Safety and Tolerability of Intravitreal MHU650 in Participants With Macular Edema From Diabetic Macular Edema (DME), Neovascular Age-related Macular Degeneration (nAMD), or Retinal Vein Occlusion (RVO)
Latest Information Update: 25 May 2023
At a glance
- Drugs MHU 650 (Primary)
- Indications Diabetic macular oedema; Retinal oedema; Retinal vein occlusion; Wet age-related macular degeneration
- Focus Adverse reactions; First in man
- Sponsors Novartis Pharmaceuticals
- 14 Sep 2022 Status changed from recruiting to completed.
- 09 Nov 2021 Planned End Date changed from 24 Mar 2022 to 25 Mar 2022.
- 26 Jan 2021 Status changed from not yet recruiting to recruiting.