Positive Phase III biosimilar infliximab study results published
Positive long-term data from a pivotal Phase III study demonstrating the clinical efficacy and safety profile of biosimilar infliximab in rheumatoid arthritis (RA) patients has been published.
After the 54-week randomised PLANETRA study, patients could participate in a 48-week extension with biosimilar infliximab Remsima. This is a biosimilar version of Johnson & Johnson's (NYSE: JNJ) Remicade. In those enrolled, efficacy and tolerability were evaluated over the full 102 weeks.
During the 48-week extension part of the study, biosimilar infliximab continued to be effective and well tolerated in RA sufferers.
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