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However, clinical observations and trial data have identified specific circumstances where these drugs may be associated with worsening diabetic retinopathy, particularly in patients with pre-existing retinal disease
This distinction matters clinically because it determines dosing, timing, and what results to expect at each stage of the protocol
The FDA has scheduled a Pharmacy Compounding Advisory Committee meeting for July 23, 2026 to review BPC-157 for the 503A Bulks List
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