Not real patients
Consistently favorable safety profile1–21
ALECENSA has a well-established, manageable
safety profile1–21
The safety profile of ALECENSA has remained consistent across multiple clinical trials and real-world studies assessing a diverse range of patients.1–21
A consistent safety profile proven over 10 years
ALECENSA has a well-established, manageable
safety profile, as shown in the ALEX final analysis2,3
The safety profile
of ALECENSA remained consistent over a longer median
follow-up of
53.5 months, with no new or unexpected safety signals observed.3
The safety profile of ALECENSA remained consistent over a
longer median follow-up of 53.45 months, with no new or unexpected safety signals observed.3
Efficacy that translates into sustained QoL improvement in ALK+ advanced NSCLC22
Clinically meaningful improvement in HRQoL (≥10 point increase)*
5 months extension in HRQoL improvement vs. crizotinib22
Patients experienced longer lasting improvements in their symptoms with ALECENSA, including22:
Chest pain
Cough
Fatigue
Dyspnea
Pain in other areas