AZD9291 Versus Placebo in Patients With Stage IB-IIIA Non-small Cell Lung Carcinoma, Following Complete Tumour Resection With or Without Adjuvant Chemotherapy.

Running, not enrolling · Phase 3 · Has a placebo group

Conditions studied: Stage IB-IIIA Non-small Cell Lung Carcinoma

In brief

To assess the efficacy and safety of AZD9291 versus Placebo, in patients with Epidermal Growth Factor Receptor Mutation Positive stage IB-IIIA non-small cell lung carcinoma, following complete tumour resection with or without adjuvant chemotherapy

Key facts

Study ID: NCT02511106
Run by: AstraZeneca
People needed: 682
Starts: 2015-10-21
Expected to finish: 2029-01-31
Last updated by the study team: 2026-03-30

Who can join

Age: 18 and older, up to 130. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Male or female, aged at least 18 years.
Histologically confirmed diagnosis of primary non small lung cancer (NSCLC) on predominantly non-squamous histology
MRI or CT scan of the brain must be done prior to surgery as it is considered standard of care.
Patients must be classified post-operatively as Stage IB, II or IIIA on the basis of pathologic criteria.
Confirmation by the central laboratory that the tumour harbours one of the 2 common EGFR mutations known to be associated with EGFR-TKI sensitivity (Ex19del, L858R), either alone or in combination with other EGFR mutations including T790M.
Complete surgical resection of the primary NSCLC is mandatory. All gross disease must have been removed at the end of surgery. All surgical margins of resection must be negative for tumour.
Complete recovery from surgery and standard post-operative therapy (if applicable) at the time of randomization.
World Health Organization Performance Status of 0 to 1.
Female patients should be using adequate contraceptive measures, should not be breast feeding, and must have a negative pregnancy test prior to first dose of study drug; or female patients must have an evidence of non-child-bearing potential.

You may not qualify if…

Treatment with any of the following:
Pre-operative or post-operative or planned radiation therapy for the current lung cancer
Pre-operative (neo-adjuvant) platinum based or other chemotherapy
Any prior anticancer therapy
Prior treatment with neoadjuvant or adjuvant EGFR-TKI at any time
Major surgery (including primary tumour surgery, excluding placement of vascular access) within 4 weeks of the first dose of study drug
Patients currently receiving medications or herbal supplements known to be potent inducers of cytochrome P450 (CYP) 3A4
Treatment with an investigational drug within five half-lives of the compound or any of its related material.
Patients who have had only segmentectomies or wedge resections
History of other malignancies, except: adequately treated non-melanoma skin cancer, curatively treated in-situ cancer, or other solid tumours curatively treated with no evidence of disease for > 5 years following the end of treatment.
Any unresolved toxicities from prior therapy greater than CTCAE Grade 1 at the time of starting study treatment with the exception of alopecia and Grade 2, prior platinum-therapy related neuropathy.
Any evidence of severe or uncontrolled systemic diseases, including uncontrolled hypertension and active bleeding diatheses; or active infection including hepatitis B, hepatitis C and human immunodeficiency virus (HIV).
Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow the formulated product, or previous significant bowel resection that would preclude adequate absorption of AZD9291.
Any of the following cardiac criteria:
Mean resting corrected QT interval (QTc) >470 msec, obtained from 3 ECGs, using the screening clinic ECG machine-derived QTc value.
Any clinically important abnormalities in rhythm, conduction, or morphology of resting ECG.
Any factors that increase the risk of QTc prolongation or risk of arrhythmic events, or unexplained sudden death under 40 years of age in first-degree relatives or any concomitant medication known to prolong the QT interval.
Past medical history of ILD, drug-induced ILD, radiation pneumonitis which required steroid treatment, or any evidence of clinically active ILD.
Inadequate bone marrow reserve or organ function.

Where it is running

Research Site — Santa Monica, California, United States
Research Site — Santa Rosa, California, United States
Research Site — Torrance, California, United States
Research Site — Grand Junction, Colorado, United States
Research Site — New Haven, Connecticut, United States
Research Site — Norwalk, Connecticut, United States
Research Site — Fort Myers, Florida, United States
Research Site — Pembroke Pines, Florida, United States
Research Site — St. Petersburg, Florida, United States
Research Site — Athens, Georgia, United States
Research Site — Honolulu, Hawaii, United States
Research Site — Chicago, Illinois, United States
Research Site — Elk Grove Village, Illinois, United States
Research Site — Bethesda, Maryland, United States
Research Site — Brick, New Jersey, United States
Research Site — Florham Park, New Jersey, United States
Research Site — Mineola, New York, United States
Research Site — Pawtucket, Rhode Island, United States
Research Site — Chattanooga, Tennessee, United States
Research Site — Nashville, Tennessee, United States
Research Site — San Antonio, Texas, United States
Research Site — Fort Belvoir, Virginia, United States
Research Site — Bedford Park, Australia
Research Site — Camperdown, Australia
Research Site — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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