
As demand for complex peptide APIs reaches unprecedented scales, manufacturers face a critical strategic question: is linear solid-phase peptide synthesis (SPPS) or a fragment-based approach the right choice for large-scale production of the target molecule?
Fragment-based approaches have gained attention following high-profile successes, but Bachem’s experience shows they are not automatically superior. To find out when – and whether – conjugation of SPPS-based fragments truly delivers advantages over optimized linear SPPS, we conducted a comprehensive feasibility study and cost evaluation on a commercially relevant GLP-1 receptor agonist.
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