iSTAR Medical receives U.S. FDA approval to start pivotal trial for MINIject in glaucoma patients
This study will report on safety and efficacy of MINIject alone, in a procedure not combined with simultaneous cataract surgery.
- This study will report on safety and efficacy of MINIject alone, in a procedure not combined with simultaneous cataract surgery.
- Patients will also be followed to evaluate long-term benefits and tolerability of MINIjectTM in the treatment of mild to moderate glaucoma.
- Michel Vanbrabant, CEO of iSTAR Medical, commented "We are very pleased that the FDA has granted us approval to bring this innovative technology to North American patients suffering from primary open angle glaucoma in the STAR-V trial.
- iSTAR Medical SA is a private med-tech company developing minimally invasive ophthalmic implants for the treatment of glaucoma patients.