We develop clinic ready, analytically-validated biosimilar
cell lines, and manufacturing processes with proven
similarity to reference compounds.
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Delivering fully validated biosimilar assets with supporting
data to jump start your development efforts.
We start every program with detailed patent discovery work, finding all valid and relevant patents in the US and EU.
We complete every aspect of analytical development for each program needed to characterize and control the biosimilar.
We screen biosimilar cell lines for each program, including single cell cloning, PQ screening, and production of a RCBs.
We develop end-to-end biosimilar processes from early upstream development through GMP drug substance production.
Our differentiated approach enables rapid biosimilar target selection, accelerates Chemistry, Manufacturing, and Controls development timelines, and reduces preclinical cost and risk. Learn more about our programs by exploring our pipelines.
Our analytical packages deliver reference product QTPP, stability data, and analytical methods at a lower cost than independent generation.
Early initiation of biosimilar development, coupled with our robust data packages, enables us to develop high quality products ready to out-license.
Reduce risk during early biosimilar development, cut costs for analytical activities, and accelerate early programs.
Are you looking for a program beyond our current pipeline but you are concerned with risks from program cancellation and market timelines? Discuss a co-development agreement with Similis to initiate the development of multiple biosimilar programs in parallel with an exclusive right to every program.
1280 N. Mathilda Ave
Sunnyvale, CA 94089
United States
+1 408 543 8800
partner@similis.bio
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