QUILT-3.036: AMG 337 in Subjects With Advanced or Metastatic Solid Tumors

This is a phase 2, two-cohort, single-arm open-label study that will assess the efficacy of
AMG 337 based on ORR in subjects with advanced or metastatic solid tumors that overexpress
MET or harbor METex14del mutations resulting in MET exon 14 skipping. MET overexpression will
be determined by quantitative proteomics with mass spectrometry. METex14del mutations
resulting in MET exon 14 skipping will be determined by DNA sequencing and confirmed with RNA
sequencing. Subjects will be enrolled as follows:

- Cohort 1: Subjects with advanced or metastatic solid tumors that overexpress MET

- Cohort 2: Subjects with advanced or metastatic solid tumors that harbor METex14del
mutations Simon's two-stage optimal design will be utilized separately for each cohort
to assess the primary efficacy endpoint ORR. The null hypothesis of Simon's two-stage
design states that the ORR will be ≤ 10% (poor response) and will be tested against a
one-sided alternative.

Inclusion Criteria:

1. Able to understand and provide a signed informed consent that fulfills the relevant
Institutional Review Board (IRB) or Independent Ethics Committee (IEC) guidelines.

2. Able to attend required study visits and return for adequate follow-up, as required by
this protocol.

3. Able to self-administer AMG 337 as a whole capsule by mouth every day.

4. Age ≥ 16 years old.

5. Histologically confirmed, unresectable locally advanced or metastatic solid tumor that
overexpresses tumor MET (determined by quantitative proteomics with mass spectrometry
[cohort 1]) or harbor METex14del mutations resulting in MET exon 14 skipping (as
determined by DNA sequencing and confirmed with RNA sequencing [cohort 2]).

6. Have measurable disease evaluable in accordance with RECIST Version 1.1.

7. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.

8. Must have a recent formalin-fixed paraffin-embedded (FFPE) tumor biopsy specimen that
was obtained following the conclusion of the most recent anticancer treatment. If a
historic specimen is not available, the subject must be willing to undergo a biopsy
during the screening period, if considered safe by the Investigator. If safety
concerns preclude collection of a biopsy during the screening period, a tumor biopsy
specimen collected prior to the conclusion of the most recent anticancer treatment may
be used.

9. Must be willing to undergo a biopsy during the treatment period, if considered safe by
the investigator.

10. Ability to attend required study visits and return for adequate follow-up, as required
by this protocol.

11. Hematologic function, as follows:

1. Absolute neutrophil count (ANC) ≥ 1.5 × 10^9/L.

2. Platelet count ≥ 50 × 10^9/L.

3. Hemoglobin > 8 g/dL.

4. Prothrombin time (PT) or partial thromboplastin time (PTT) < 1.5 × upper limit of
normal (ULN), except for subjects on anticoagulation therapy for venous
thromboembolism.

12. Renal function, as follows:

a. Calculated creatinine clearance > 30 mL/min.

13. Hepatic function, as follows:

1. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 2.5 × ULN
and total bilirubin < 1.5 × ULN.

2. Alkaline phosphatase (ALP) < 2 × ULN (≤ 5 × ULN if bone or liver metastases are
present).

14. Agreement to practice effective contraception (both male and female subjects, if the
risk of conception exists).

Exclusion Criteria:

1. Assessed by the investigator to be unable or unwilling to comply with the requirements
of the protocol.

2. Inability to attend required study visits and return for adequate follow-up, as
required for this protocol.

3. Known hypersensitivity to any component of the study medication(s).

4. Women who are nursing, pregnant, or planning to become pregnant during the duration of
the study.

5. Current diagnosis of sporadic or hereditary renal cell carcinoma.

6. Current diagnosis or history of a second neoplasm, except the following:

a. Adequately treated non-melanoma skin cancer, curatively treated in situ disease, or
other solid tumors curatively treated with no evidence of disease for ≥ 2 years.

7. Subjects with tumors with ALK-positive rearrangement who received prior treatment with
crizotinib.

8. History of bleeding diathesis.

9. Uncontrolled hypertension (systolic > 160 mmHg and/or diastolic > 100 mmHg) or
clinically significant cardiovascular disease, cerebrovascular accident/stroke, or
myocardial infarction within 6 months before study day 1; unstable angina; congestive
heart failure of New York Heart Association grade 2 or higher; or serious cardiac
arrhythmia requiring medication.

10. Baseline ECG Fridericia's formula (QTcF) > 470 ms.

11. Active infection requiring IV antibiotics within 2 weeks before study day 1.

12. Significant gastrointestinal disorder (eg, Crohn's disease, ulcerative colitis,
extensive gastrointestinal resection) that in the opinion of the investigator may
influence drug absorption.

13. Positive result of screening test for human immunodeficiency virus (HIV).

14. Evidence of acute hepatitis B and C. Subjects with chronic hepatitis B or C are
eligible if their condition is stable and, in the opinion of the investigator, would
not pose a risk to subject safety.

15. Toxicities from prior anti-tumor therapy not resolved to CTCAE Version 4.03 grade 0 or
1.

a. Grade 2 toxicities from prior antitumor therapy that are considered irreversible
(defined as having been present or stable for > 4 weeks), such as stable grade 2
peripheral neuropathy or ifosfamide-related proteinuria, may be allowed if they are
not otherwise described in the exclusion criteria.

16. Participation in this study or in an investigational study and/or procedure with any
molecularly targeted agents reported to inhibit MET within 14 days before study day 1.

17. Antitumor therapy, including chemotherapy, antibody therapy, retinoid therapy, or
other investigational therapy, within 14 days before study day 1.

18. Therapeutic or palliative radiation therapy within 14 days before study day 1.

19. Major surgery within 28 days before study day 1.

20. Any comorbidity that in the opinion of the investigator may increase the risk of
toxicity.

21. Concurrent or prior use of a strong CYP3A4 inhibitor within 14 days before study day
1, including the following: ketoconazole, itraconazole, clarithromycin, indinavir,
nefazodone, nelfinavir, ritonavir, saquinavir, telithromycin, and voriconazole.

22. Concurrent or prior ingestion of grapefruit, grapefruit products, or other foods known
to inhibit CYP3A4 within 7 days before study day 1.

23. Concurrent or prior use of strong CYP3A4 inducers within 28 days before study day 1,
including the following: phenytoin, carbamazepine, rifampin, rifabutin, rifapentin,
phenobarbital, and the herbal supplement St. John's Wort.