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Zepbound is FDA approved and covered by Part D for this indication, so patients with moderate to severe OSA are directed to their Part D plan rather than the Bridge

This distinction matters not just to drug developers, but to the broader drug manufacturing market: as peptide drug volumes scale, demand surges for the reagents, instrumentation, contract manufacturing capacity, and analytical workflows that underpin both approaches

No serious adverse effects were reported across the trials

Regulatory guidelines require detailed analytical characterization before a biosimilar product can enter the market