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Profesionales

Gabín María Noel


Oftalmología - Médica de staff / Oftalmología Infantil - Médica de staff

Formación

Médica

Especialización

  • Residencia completa hospital Medalla Milagrosa.
  • Fellowship Retina HUA.
  • Especialista Oftalmología USAL.

Antecedentes

  • Medica de Planta HUA
  • A cargo del Servicio de Oftalmología Hospital Comodoro Meisner, Pilar Pcia de Buenos Aires.
  • A cargo del Servicio de Oftalmología Hospital Nuestra Señora del Pilar, Pilar Pcia de Buenos Aires.

Docencia

  • Ayudante de cátedra Fisiología (endocrinología-neurolofisiología) Escuela de medicina Hospital Italiano.

Participación

SANTEN

Study 32-007 “A Phase III, Multinational, Multicenter, Randomized, Double-Masked, Study Assessing the Safety and Efficacy of Intravitreal Injections of DE-109 (three doses) for the Treatment of Active, Non-Infectious Uveitis of the Posterior Segment of the Eye” SANTEN INCORPORATED

GENENTECH

Study FVF 4168g “A PHASE III, DOUBLE-MASKED, MULTICENTER, RANDOMIZED, SHAM INJECTION–CONTROLLED STUDY OF THE EFFICACY AND SAFETY OF RANIBIZUMAB INJECTION IN SUBJECTS WITH CLINICALLY SIGNIFICANT MACULAR EDEMA WITH CENTER INVOLVEMENT SECONDARY TO DIABETES MELLITUS” GENENTECH

ABBOT

Study M10-880 “Phase III study, A Multicenter Study of the Efficacy and Safety of the Human Anti-TNF Monoclonal Antibody Adalimumab as Maintenance Therapy in Subjects Requiring High Dose Corticosteroids for Active Non-infectious Intermediate-, Posterior-, or Pan-uveitis” VISUAL I. AbbVIE (Abbott)

Study M10-877 “Phase III study, A Multicenter Study of the Efficacy and Safety of the Human Anti-TNF Monoclonal Antibody Adalimumab in Subjects With Inactive Non-infectious Intermediate-, Posterior-, or Pan-uveitis” – VISUAL II. AbbVIE (Abbott)

Study M10-327 “phase iii study, A Multicenter Open-Label Study of the Long-term Safety and Efficacy of the Human Anti-TNF Monoclonal Antibody Adalimumab in Subjects With Noninfectious Intermediate-, Posterior-, or Pan-uveitis” – VISUAL III. AbbVIE (Abbott)

OPHTHOTECH

STUDY OPH1003 ”FOVISTA”. A PHASE 3 RANDOMIZED, DOUBLE-MASKED, CONTROLLED TRIAL TO ESTABLISH THE SAFETY AND EFFICACY OF INTRAVITREOUS ADMINISTRATION OF FOVISTATM (ANTI PDGF-B PEGYLATED APTAMER) ADMINISTERED IN COMBINATION WITH LUCENTIS® COMPARED TO LUCENTIS® MONOTHERAPY IN SUBJECTS WITH

SUBFOVEAL NEOVASCULAR AGE-RELATED MACULAR DEGENERATION. opHtHOTECH

ALCON (AZARGA)

Study RDG 11-198 “phase iii study, Assessing the Efficacy and Tolerability of AZARGA® (Brinzolamide 1%/Timolol 0.5% Fixed Combination) as Replacement Therapy in Patients on Brimonidine 0.2%/Timolol 0.5% Fixed Combination Therapy (COMBIGAN®) in Latin America” Alcon

Acreditado por Joint Commission InternationalOAAMiembro de la Red Global de Hospitales Verdes y Saludables