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Bispecific DP Development Stability
Aurigene engineered a stable bispecific drug product formulation across both lyophilized and liquid presentations through rapid excipient evaluation, fill volume studies, and optimized lyophilization recipe design. The result: <1% aggregation across stability conditions, <2% moisture in final Lyo DP, buffer/pH identified in just 14 days, and a cGMP DP batch delivered within 4 weeks — cutting development timelines by 40% versus industry average.
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