The complexity of small molecule active pharmaceutical ingredients (APIs) is rising, bringing longer syntheses that challenge innovators' timely readiness for the Clinic.
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Better, faster small-molecule synthesis: leveraging modern tools to evaluate and optimize process chemistry
This white paper details a collaborative effort between Lonza’s Bend, OR site and Pfizer’s Groton, CT team to develop a robust commercial control strategy for a pediatric dosage form for crizotinib (Xalkori) in a material sparing fashion.
Bioconjugates are no longer just for cancer therapies. This paper reveals how innovative advancements are opening up a new world of possibilities, from muscle disorders to inflammatory diseases.
In an era of precision medicine and adaptive clinical trial designs, dose flexibility is no longer optional—it’s essential. From preclinical development to commercialization, the ability to scale, modify, and tailor dose strengths is key to meeting regulatory expectations and optimizing patient-centered therapies.
The shift toward biologics delivered via the respiratory route is accelerating—and with it comes the need for precision in excipient selection. Whether in nebulized liquids or dry powder inhalers, biologics demand tailored formulation strategies to ensure safety, stability, and therapeutic effectiveness.
Efficient tech transfer is critical to the success of every Oral Solid Dosage (OSD) product—especially when transitioning from development to full-scale commercial manufacturing.