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CLAIM #43424 · Merck & Company Inc (MRK) · 2024Q1 earnings call · Apr 25, 2024 · due Dec 31, 2028

Obviously, if you look at then the size of the patient population where it could be, just to give you a sense, by 2028, if we look at the patients who are on monotherapy with KEYTRUDA who are using combinations with orals and those who are moving into earlier stages of disease through some of our adjuvant and neoadjuvant areas with KEYTRUDA, that represents about 50% of the patient population at that time.

Rob Davis · CEO

PENDING
graded after results covering Dec 31, 2028 are reported

How to check this claim

Look at: Patients on KEYTRUDA monotherapy, combinations with orals, and those in adjuvant/neoadjuvant (earlier-stage disease) settings, as a percentage of the total KEYTRUDA-treated (or addressable) patient population

It came true if: Reported or estimated share of this patient segment >= 45% of total addressable population by 2028

Where: Company disclosures, investor presentations, or management commentary on KEYTRUDA patient population segmentation (10-K/earnings calls through 2028)

In context

.. Robert Davis: Yes. Maybe, Tim, I'll just provide some commentary on your questions on uptake and how much of the patient population this can account for. As we think about uptake of this opportunity, I would first point out that we see really -- it starts with the strength of the clinical data underlying the IO agent itself. So it's more about the confidence they have in KEYTRUDA. And then secondarily, it's about the delivery mechanism, which is important as we think about obviously leveraging the data we have and just the breadth of what KEYTRUDA is. But I will tell you that as we think about bringing this forward when we do launch, our goal will be the price appropriately with the goal of driving quick adoption. So we do want to see adoption happen, and we do think you will see it. Obviously, if you look at then the size of the patient population where it could be, just to give you a sense, by 2028, if we look at the patients who are on monotherapy with KEYTRUDA who are using combinations with orals and those who are moving into earlier stages of disease through some of our adjuvant and neoadjuvant areas with KEYTRUDA, that represents about 50% of the patient population at that time. So that is really the addressable market for what we see the subcu offering to be. And potentially, we're not foreclosing the opportunity to also look into the metastatic setting and people being given care in institutions as well as those moving outside of the institutions. But obviously, the value to the patient is ease of use, ability to use it outside of the hospital setting. The time and share is obviously less if you're getting a subcu versus an IV. And then from a cost to the health care system, the ability to not have a patient sitting in the chair for as long allowing for more patients to move through, we think, actually drives access and improves the providing of care as well. So we see it both beneficial from a patient perspective and from the provider perspective, and that's

Verify independently

SEC filings for MRK · Claim quote is verbatim from the 2024Q1 earnings call.