Docetaxel With or Without FGFR Inhibitor AZD4547 in Treating Patients With Recurrent Non-Small Cell Lung Cancer

PRIMARY OBJECTIVES:

I. Determination of a recommended phase II dose for the combination of docetaxel and AZD4547
(FGFR inhibitor AZD4547). (Phase I) II. Estimation and comparison of progression-free
survival (PFS) of each treatment arm. (Phase II)

SECONDARY OBJECTIVES:

I. Pharmacokinetic evaluation of docetaxel with or without concomitant AZD4547.
Pharmacokinetic evaluation of AZD4547 with concomitant docetaxel. (Phase I) II. Safety
assessment and toxicity characterization of the combination. (Phase I) III. Initial
assessment of clinical activity of the combination. (Phase I) IV. Response rate. (Phase II)
V. Overall survival. (Phase II) VI. Estimation of response to single agent AZD4547 among
patients who crossover from single agent docetaxel. (Phase II) VII. Further safety assessment
and toxicity characterization of AZD4547 alone and in combination with docetaxel. (Phase II)

OUTLINE: This is a phase I, dose-escalation study of FGFR inhibitor AZD4547 followed by a
randomized phase II study.

PHASE I:

Patients receive docetaxel intravenously (IV) over 60 minutes on day 1 and FGFR inhibitor
AZD4547 orally (PO) twice daily (BID) on days 2-15 of course 1 and days 1-14 of all
subsequent courses. Courses repeat every 21 days in the absence of disease progression or
unacceptable toxicity.

PHASE II, STEP I: Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients receive docetaxel IV over 60 minutes on day 1. Treatment repeats every 21
days for up to 6 courses in the absence of disease progression or unacceptable toxicity.
Patients who experience progressive disease may then receive FGFR inhibitor AZD4547 PO BID on
days 1-14.

ARM II: Patients receive docetaxel IV as in Arm I and FGFR inhibitor AZD4547 PO BID on days
1-14.

In both arms, courses repeat every 21 days in the absence of disease progression or
unacceptable toxicity.

PHASE II, STEP II:

Patients receive FGFR inhibitor AZD4547 PO BID on days 1-14. Courses repeat every 21 days in
the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up for 3 years.

This study opened to accrual on September 19, 2013 and was suspended to accrual on January
29, 2014 after each of the first two patients had been registered to the first dose level of
the phase I and experienced dose limiting toxicities (DLTs) during week 1 of cycle 1. The
study was subsequently terminated on April 17, 2014 after having met the predefined criteria
for closure per the phase I study design.

Phase I:

Inclusion Criteria:

- All females of childbearing potential must have a blood test or urine study within 2
weeks prior to registration to rule out pregnancy

- Women of childbearing potential and sexually active males must agree to use adequate
contraception (hormonal or barrier method of birth control; abstinence) prior to study
entry and for the duration of study participation; should a woman become pregnant or
suspect she is pregnant while participating in this study, she should inform her
treating physician immediately

- Measurable or non-measureable disease based on Response Evaluation Criteria in Solid
Tumors (RECIST) 1.1; baseline measurements and evaluations of all sites of disease
must be obtained =< 4 weeks prior to registration

- Histologically or pathologically confirmed squamous NSCLC; patients whose tumors
contain mixed NSCLC histologies are eligible if squamous morphology is predominant;
mixed tumors with small cell anaplastic elements are not eligible

- Life expectancy >= 12 weeks

- Eastern Cooperative Oncology Group (ECOG) performance status 0 - 1

- Adequate organ and marrow function

- Mean resting corrected QT interval (QTc) < 470 msec obtained from 3 consecutive
electrocardiograms

Exclusion Criteria:

- Pregnant or breast-feeding women

- Clinically important abnormalities in rhythm, conduction or morphology of resting
electrocardiogram (ECG) e.g. complete left bundle branch block, third degree heart
block

- Factors that increase the risk of QTc prolongation or risk of arrhythmic events such
as heart failure, hypokalemia, congenital long QT syndrome, family history of long QT
syndrome or unexplained sudden death under 40 years of age or any concomitant
medication known to prolong the QT interval

- Prior treatment with docetaxel (except in the adjuvant setting), or AZD4547

- Prior treatment with any other chemotherapy, immunotherapy or anticancer agents within
2 weeks prior to registration

- Current evidence or previous history of retinal pigmented epithelium detachment (RPED)

- Previous laser treatment or intra-ocular injection for treatment of macular
degeneration

- Current evidence or previous history of dry or wet age-related macular degeneration

- Current evidence or previous history of retinal vein occlusion (RVO)

- Current evidence or previous history of retinal degenerative diseases (e.g.
hereditary)

- Current evidence or previous history of any other clinically relevant chorioretinal
defect

- Uncontrolled brain metastases

- History of allergic reactions attributed to compounds of similar chemical or biologic
composition to AZD4547, docetaxel or other agents used in the study

- Uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia, or psychiatric illness/social situations that would limit compliance with
study requirements

- Refractory nausea and vomiting, chronic gastrointestinal disease, inability to swallow
the investigational drug, previous significant bowel resection, or any other
significant gastrointestinal disorder that could, in the opinion of the Investigator,
interfere with the absorption of AZD4547

- Major surgical procedure within 3 weeks prior to registration

- Grade 3 or higher peripheral neuropathy, as defined by the National Cancer Institute
(NCI) Common Terminology Criteria for Adverse Events (CTCAE),version 4.02

- Known hepatitis B virus (HBV) or hepatitis C virus (HCV) infection

- Known human immunodeficiency virus (HIV) with cluster of differentiation (CD)4 count
is =< 200 cell/mm^3 or receiving antiretroviral therapy due to potential unfavorable
interactions of the agents with the study treatment

- Receiving any other investigational agents while on study

- Medications that are potent inhibitors of cytochrome P450, family 3, subfamily A,
polypeptide 4 (CYP3A4), cytochrome P450, family 2, subfamily C, polypeptide 8
(CYP2C8), cytochrome P450, family 2, subfamily D, polypeptide 6 (CYP2D6), or
substrates of CYP3A4 prior to the first dose of study treatment

Phase II pre-registration:

- Patient must have paraffin-embedded tumor specimen available for submission for
determination of fibroblast growth factor receptor 1(FGFR1) amplification status

Phase II Step I - Randomization:

- Besides the eligibility criteria in Step I, patient must have positive tumor FGFR1
gene amplification (score FISH6) as determined by an AstraZeneca approved central
laboratory.

Phase II Step II:

Inclusion Criteria:

- Patient was randomized to docetaxel only on step 1 and progressed per RECIST v1.1
criteria; registration to step 2 must occur within 4 weeks of
confirmation/determination of disease progression

- Confirmed measurable disease based on RECIST 1.1; baseline measurements and
evaluations of all sites of disease must be obtained =< 4 weeks prior to registration

Exclusion Criteria:

- Pregnant or breast-feeding women