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A Study of the Efficacy and Safety of Alectinib in Participants With Anaplastic Lymphoma Kinase (ALK)-Rearranged Non-Small Cell Lung Cancer
- Cancer
- Lung Cancer
- Non-Small Cell Lung Cancer (NSCLC)
Please note that the recruitment status of the trial at your site may differ from the overall study status because some study sites may recruit earlier than others.
Trial Status:
Completed
This trial runs in
Cities
- Angers
- Besançon
- Brest
- Caen
- Créteil
- La Tronche
- Lille
- Marseille
- Mulhouse
- Paris
- Pessac
- Rennes
- Rouen
- Toulouse
- Vantoux
Trial Identifier:
NCT03155009 2016-003924-22 ML39349
Trial Summary
This study will evaluate the efficacy and safety of alectinib, in selected participants, with anaplastic lymphoma kinase-rearranged (ALK-rearranged) non-small cell lung cancer (NSCLC), after disease progression on prior treatment strategy with crizotinib, as only ALK inhibitor, and eventually chemotherapy treatment(s).
Hoffmann-La Roche
Sponsor
Phase 2
Phase
NCT03155009,ML39349,2016-003924-22
Trial Identifier
Alectinib
Treatments
Carcinoma, Non-Small-Cell Lung
Condition
Official Title
An Open-Label, Multicenter, Single-Arm, Phase II Study to Assess the Efficacy and Safety of Alectinib in Patients With ALK-Rearranged Non-Small Cell Lung Cancer After Disease Progression on Prior ALK Inhibitor Therapy
Eligibility Criteria
All
Gender
≥ 18 Years
Age
No
Healthy Volunteers
Inclusion Criteria
- Participants with histologically or cytologically confirmed locally advanced or metastatic NSCLC (Stage IIIB or IV accordingly to American Joint Committee on Cancer [AJCC] classification)
- Life expectancy of at least 12 weeks, in the opinion of the Investigator
- Eastern Cooperative Oncology Group Performance Status (ECOG PS) ≤ 2
- Having contributive biopsy performed on fresh tissue (FFPE blocks required) taken after progression on previous therapy showing presence of anaplastic lymphoma kinase (ALK) rearrangement, assessed by immunohistochemistry (IHC) and confirmed by fluorescence in situ hybridization (FISH)
- Absence of resistance mechanism to alectinib assessed by the Biomarkers Board
- Disease progression, limited to central nervous system (CNS) without possibility of tissue biopsy
- Non-contributive molecular analyses (not enough tumor cells or deoxyribonucleic acid, [DNA] amount or failure of analyses for technical reasons): inclusion is at investigator discretion (decision made upon Biomarker Board recommendation)
- History of crizotinib exposure
- Washout period: if previous progression on crizotinib: 7 days from last intake of the drug
- If previous progression on chemotherapy: 28 days
- If previous radiation therapy: 15 days
- Participants must have recovered from treatment toxicities to ≤ Grade 1 or to their pretreatment levels (for participants who have developed interstitial lung disease [ILD], they must have fully recovered)
- Recovery from effects of any major surgery, or significant traumatic injury, at least 35 days before the first dose of alectinib
- Adequate hematologic function
- Adequate renal function
- For all females of childbearing potential, a negative pregnancy test must be obtained within three days before starting study drug
- For women who are not postmenopausal (≥ 12 months of non-therapy-induced amenorrhea) or surgically sterile (absence of ovaries and/or uterus): agreement to remain abstinent or use two adequate methods of contraception, including at least one method with a failure rate of < 1% per year, during the treatment period and for at least 90 days after the last dose of study drug
- For men: agreement to remain abstinent or use a barrier method of contraception (e.g., condom) during the treatment period and for at least 90 days after the last dose of study drug and agreement to refrain from donating sperm during this same period
- Participant has national health insurance coverage
Exclusion Criteria
- Prior therapy with other ALK inhibitors than crizotinib (including alectinib)
- Participants with symptomatic CNS metastases who are neurologically unstable or require increasing doses of steroids within one week prior to Day 0 to manage CNS symptoms
- Participants with progression limited to CNS and eligible to a focal treatment (surgery or stereotaxic radiotherapy)
- Administration of strong/ potent cytochrome P450 3A (CYP3A) inhibitors or inducers, or agents with potential QT prolonging effects within 14 days prior to first administration of study drug
- Liver disease
- Any clinically significant concomitant disease or condition that could interfere with, or for which the treatment might interfere with, the conduct of the study or the absorption of oral medications or that would, in the opinion of the investigator, pose an unacceptable risk to the participant in this study
- Active or uncontrolled infectious diseases requiring treatment
- History of organ transplant
- Participants with baseline QTc > 470 ms or participants with symptomatic bradycardia
- Pregnant or lactating women
- History of hypersensitivity to any of the additives in the alectinib drug
- Any psychological, familial, sociological, or geographical condition potentially hampering compliance with the study protocol requirements and/or follow-up procedures; those conditions should be discussed with the participant before trial entry
- Serious, uncontrolled infections or current known infection with human immunodeficiency virus (HIV).
For the latest version of this information please go to www.forpatients.roche.com