A Phase I/IIa Dose Escalation Safety Study of Subretinally Injected SAR421869, Administered to Patients with Retinitis Pigmentosa Associated with Usher Syndrome Type 1B
Latest Information Update: 07 Nov 2021
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At a glance
- Drugs SAR 421869 (Primary)
- Indications Usher syndromes
- Focus Adverse reactions; First in man
- Sponsors Oxford BioMedica; Sanofi
- 26 Sep 2019 Status changed from recruiting to discontinued.
- 28 Jan 2019 Planned number of patients changed from 18 to 27.
- 13 Jul 2018 Planned End Date changed from 24 Feb 2020 to 13 Jan 2021.