Regeneron is scheduled to resume trading at 3:15 pm ET, with quotation set to resume at 3:10 pm ET, according to Nasdaq. Shares were halted pending news ahead of Regeneron Pharmaceuticals announcing that the FDA has issued a Complete Response Letter, or CRL, for the Biologics License Application, or BLA, for aflibercept 8 mg for the treatment of patients with wet age-related macular degeneration, diabetic macular edema and diabetic retinopathy and also announcing top-line, two-year data for aflibercept 8 mg from the pivotal PHOTON trial in patients with diabetic macular edema.
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Read More on REGN:
- REGN, CTLT Continue Sliding Following FDA Rejection of Eylea Drug
- Regeneron Stock (NASDAQ:REGN) Sinks; FDA Snubs Higher-Dose Eye Drug
- FDA Issues Complete Response Letter (CRL) for Aflibercept 8 mg Biologics License Application Solely Due to an Ongoing Review of Inspection Findings at a Third-party Filler
- Two-year Results for Aflibercept 8 mg from Pivotal PHOTON Trial Demonstrate Durable Vision Gains at Extended Dosing Intervals in Diabetic Macular Edema
- Regeneron’s two-year Eylea data should look ‘consistent’, says RBC Capital