CROWN trial2
LORBRIQUA® is a third-generation ALK inhibitor that was evaluated in a global, open-label, randomised, multicentre, Phase 3 trial2
Adapted from Shaw AT, et al. 2020.
Primary endpoint
Secondary endpoints:
Baseline Characteristics2
Adapted from Shaw AT, et al. 2020.
*Based on the BICR assessment.
ALK, anaplastic lymphoma kinase; ALK+, anaplastic lymphoma kinase-positive; BICR, blinded independent central review; BID, twice a day; CNS, central nervous system; DoR, duration of response; ECOG PS, Eastern Cooperative Oncology Group performance status; IC, intracranial; IC-DoR, intracranial duration of response; IC-ORR, intracranial overall response rate; IQR, interquartile range; NSCLC, non-small cell lung cancer; ORR, objective response rate; OS, overall survival; PFS, progression-free survival; QD, once a day; QoL, quality of life; RECIST v1.1, Response Evaluation Criteria in Solid Tumours version 1.1.
References:
Please click the Prescribing Information link to view the safety and adverse events information of LORBRIQUA®.
For the use only of Registered Medical Practitioners or a Hospital or a Laboratory.
PP-LOR-IND-0129 June 2022
82% IC response rate with LORBRIQUA® in patients with measurable brain metastases at baseline (BICR assessed)
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