Investor Presentaiton
Investor Presentation
First six months of 2018
Slide 77
5 out of 10 PIONEER trials for oral semaglutide are
completed, rest are expected to read out during H2 2018
2016
Q1 2018¹ Q2 2018¹ Q3 2018¹ Q4 2018¹
PIONEER 3: vs sitagliptin²
78 weeks, n=1,860
PIONEER 1: monotherapy²
26 weeks, n=704
PIONEER 2: vs empagliflozin²
52 weeks, n=816
2017
PIONEER 4: vs liraglutide²
52 weeks, n=690
PIONEER 5: moderate renal impairment²
26 weeks, n=324
PIONEER 6: cardiovascular outcomes³
Event driven (>122 MACE), n=3,176
PIONEER 7: flexible dose escalation4
52 weeks, n=500
PIONEER 8: insulin add-on²
26+26 weeks, n=720
PIONEER 9: JAPAN monotherapy²
52 weeks, n=230
PIONEER 10: JAPAN OAD combination4
52 weeks, n=336
1 Expected to be published in the given quarter or in the subsequent quarterly company announcement. Estimated timing from first patient first visit to completion of trial
2 Primary endpoint after 26 weeks of treatment by using the statistical method: Treatment policy estimand approach
3 Primary endpoint after 122 major adverse cardiovascular events (MACE), defined by non-fatal stroke, non-fatal myocardial infarction or CV death
Chama endpoint after 52 weeks of treatment by using the statistical method: Treatment policy estimand approach
diabetes pproximate number of randomised people; OAD: oral anti-diabetic
52 weeks extension trial
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