|Articles|June 15, 2003

Bausch & Lomb to delay regulatory filing

Rochester, NY-Bausch & Lomb will delay the regulatory filing for the intravitreal fluocinolone acetonide implant (Retisert), a treatment for diabetic macular edema (DME), for up to 3 years while the FDA reviews 12-month safety data of additional eyes treated with implants.

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Bausch & Lomb to delay regulatory filing

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