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If Merck succeeds in transitioning a substantial portion of the Keytruda patient base to the subcutaneous version by 2026 or 2027, the commercial position of IV pembrolizumab biosimilars, which would launch against the original IV formulation, is materially weakened
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They are primarily prescribed for patients with type 2 diabetes and may have side effects such as nausea, diarrhea, and constipation
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