Biosimilar adoption
Scott: We've had this recent wave of biologic products and I think one of the recent bright spots is really the emergence of biosimilar options for biologic drugs such as Humira® and Stelara®. You know, these are products used to treat conditions like rheumatoid arthritis, psoriasis, and Crohn's disease. Where are we in terms of biosimilar adoption now and what do you anticipate going forward?
John: When you're thinking about cost, there's clearly an importance to biosimilars because they provide a real opportunity to get clinically equivalent products at less expense. At Optum we have defined formular strategies and principles around biosimilars that we are beginning to deploy.
For example, we've excluded Humira starting January 1st and we're working with providers to get people on biosimilars without sacrificing the clinical care model and making sure that it's appropriate for patients.
A really important key for us is that alignment with providers to make sure that they're on board with clinically equivalent products. Then we also need to make sure that patients who may have been used to a certain therapy in the past realizes this new biosimilar is just as efficacious and safe but at a lower cost.
Obviously, there is a significant impact that can happen to trend in savings, but there are also complexities beyond what the provider impact is and the patient impact is. Having a significant number of patients on the product with a client is really important to making those savings really count. So, we're really trying to take all of that into consideration. We do not want to sacrifice the patient experience but it represents a really important lever for us with our clients.