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Estás en:  / Home  /  investigation   /  A multicentre, randomized, double masked, 4-parallel, controlled, 6-month phase II study to assess the safety and efficacy of a cyclosporine PAD ophthalmic dispersion (0.06% and 0.03% CsA). Administered once daily in combination with lubricant therapy and safety monitoring three months after treatment in patients with moderate to severe xerophthalmia.
LASTEST ACTIVITIES

 

RESEARCHER:

Dr. Jesús Merayo Lloves

 ACTIVO 

 

A multicentre, randomized, double masked, 4-parallel, controlled, 6-month phase II study to assess the safety and efficacy of a cyclosporine PAD ophthalmic dispersion (0.06% and 0.03% CsA). Administered once daily in combination with lubricant therapy and safety monitoring three months after treatment in patients with moderate to severe xerophthalmia.


INDICATION: Moderate to severe dry eye
TREATMENT: Ciclosporina
PROMOTOR: Mc2 biotec- Iris Pharma