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Table 4 presents the results per indication class and benefit category.
They present the minimum and the maximum mean discount when comparing discounts per indication class (Tables 1 and 2).
By relying on drug compounds already approved for humans, the company is able to commercialize FDA-approved treatments in three to five years, including the clinical trial period, and at a cost of about $5 million per indication.
Most likely the opinions of patients differ per indication.
The yield of advanced neoplasia per indication group is shown in Table 1.
But doses per indication vary by institution and by the patient's size, and national averages simply aren't available.
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In addition, we determined per-indication compliance for Moment 1 and Moment 4, as well as compliance for opportunities that combined Moments 1 and 4. Opportunities considered for this two-indication group were mutually exclusive with the opportunities used in the single indication measures.
Per approved indication, endocrine treatment naive patients were assigned to palbociclib plus letrozole (PAL+LET) or letrozole alone (LET).
Filgrastim was used for a mean (SD) of 4.8 (3.3) injections per cycle compared to 1.0 (0.2) injections per cycle with pegfilgrastim, which was consistent with pegfilgrastim's once-per-cycle indication.
For example, the patient population in VECTIS was unselected and included all the patients who were eligible for panitumumab monotherapy, as per licensed indication.
Clinical records of patients diagnosed with mild-to-moderate IPF (as per European Medicines Agency indication) and receiving pirfenidone treatment across three centers in Belgium and the Netherlands between April 2011 and October 2013 were retrospectively collected from patient notes at 3-month intervals.
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CEO of Professional Science Editing for Scientists @ prosciediting.com