Why the study?
The complex nature of LMWH molecules creates uncertainty about chemical identity and activity differences between LMWH biosimilars and reference products, challenging evidence evaluation for clinical use.
A working group consensus emphasizes the need for prospective clinical studies and post-marketing pharmacovigilance to ensure the safety and efficacy of LMWH biosimilars compared to reference products.
Urges caution before adopting LMWH biosimilars without dedicated trial data; confirms necessity of prospective RCTs for this class.
A working group of clinicians and scientists was formed to review the clinical considerations for use of low-molecular-weight heparin (LMWH) biosimilars. LMWH are biological molecules of significant complexity; the full complexity of chemical structure is still to be elucidated. LMWH biosimilars are products that are biologically similar to their reference product and rely on clinical data from a reference product to establish safety and efficacy. The complex nature of LMWH molecules means that it is uncertain whether a LMWH biosimilar is chemically identical to its reference product; this introduces the possibility of differences in activity and immunogenicity. The challenge for regulators and clinicians is to evaluate the level of evidence required to demonstrate that a LMWH is sufficiently similar to the reference product. The consensus opinion of the working group is that prior to clinical use a LMWH biosimilar should have proven efficacy and safety, similar to the reference product with prospective studies, which should be confirmed with a proactive post-marketing pharmacovigilance programme.
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Nandurkar et al. (2014) conducted a review in Low-molecular-weight heparin (LMWH) biosimilars use. Low-molecular-weight heparin (LMWH) biosimilars vs. Reference product was evaluated. Low-molecular-weight heparin biosimilars should demonstrate proven efficacy and safety similar to the reference product in prospective studies prior to clinical use.
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