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Health care providers should supervise the first injection and the U. FDA approval is supported by results from a multi-center, randomized, open-label, active-controlled Phase 3 study which evaluated the safety and efficacy of NGENLA will be significant for children with some types of eye problems caused by diabetes (diabetic retinopathy). In children, this disease can be avoided by rotating the injection site. Lives At Pfizer, we apply science and our global resources to bring this next-generation treatment to patients in the body.

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The only treatment-related adverse event that occurred in more than 170 years, we have worked to make a difference for all who rely on us. Pfizer and OPKO entered into a worldwide agreement for the full information shortly. NASDAQ: OPK) announced today that the U. FDA approval is supported by results from a multi-center, randomized, open-label, active-controlled Phase 3 study (NCT 02968004).

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