We usually like to at least start with a data-driven approach using our databases. We will typically align with the client on quantitative-based metrics to use to feed into our prioritization. Things like, what are the current sales for the indication, are those indications forecasted to grow in sales? We can look at things like competitive intensity. How many drugs are in the pipeline at the moment? How many drugs are marketed? What do we think the unmet need is going to be?
Then once we have some quantitative metrics, we will usually build and extract the high-level indication information from our databases. And we will build a prioritization model that the client can use to weigh different aspects depending on how they want to test different scenarios, and it will rank the indications just based on the data.
Once we have got the top view from those models, we will then do further due diligence either through secondary or primary research. For instance, we can test the TPP (target product profile) with the KOLs (key opinion leaders) to see for your particular product, which indication do KOLs think is going to be best? The client provides information on their product, such as the expected efficacy and safety, and we will interview key opinion leaders and ask them, on a scale of 1 to 10, how would you rate the product? Where do you think it will be best situated? Would you prescribe it? And that information can feed into these prioritization exercises.
The typical stakeholders can vary quite a lot depending on the client. On these types of projects, I’ve worked with people on the business development side of things, but I’ve also had stakeholders from the clinical team as well. Usually it does mean having to present to a wide range of different stakeholders and trying to mesh everyone’s different opinions.