Table 2.
Statement | Important/Extremely Important | Selected as Being in the Three Most Important Statements |
---|---|---|
Studies that provide clinical immunogenicity data for the biosimilar and reference product | 97% | 42% |
Studies that directly compare clinical efficacy and safety between reference products and biosimilars | 96% | 68% |
Studies that show pharmacokinetic similarities between reference products and biosimilars | 96% | 30% |
Inclusion in international and Russian clinical practice guidelines and standards of treatment | 95% | 55% |
Studies that show chemical/physical similarities between reference products and biosimilars | 89% | 24% |
Studies that compare activity with in vitro functional assays between reference products and biosimilars | 87% | 21% |
Acquisition cost differences | 78% | 31% |
Colleague and expert opinion | 78% | 8% |
Payer decisions and requirements | 69% | 21% |
Data were extracted from question 10 of the questionnaire (see Survey Questionnaire 1).