Overview

A Phase 1 Study Evaluating CB-5083 in Subjects With Advanced Solid Tumors

Status:
Terminated
Trial end date:
2017-08-25
Target enrollment:
0
Participant gender:
All
Summary
This is a multicenter, open-label, Phase 1 study of orally administered CB-5083 in adult subjects with advanced metastatic solid tumors. The study will be conducted in 2 parts: an initial Dose Escalation Phase (Phase 1a) of CB-5083 in subjects with advanced metastatic solid tumors who have progressed or are non-responsive to available therapies and for which no standard therapy exists, followed by a Dose Expansion Phase (Phase 1b) which will include 1 to 4 arms: one arm in subjects with RAS mutated mCRC; optionally, at sponsors discretion, 3 additional arms may be added for subjects with advanced RCC, advanced pNET, or solid tumors with mutations in the RAS-MAPK pathway.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Cleave Biosciences, Inc.
Criteria
Inclusion Criteria - All Phases:

1. Males and females ≥18 years of age;

2. Eastern Cooperative Oncology Group (ECOG) Performance Status of ≤1

3. Acceptable bone marrow and organ function at screening as described below:

1. ANC ≥ 1,500/µL;

2. Platelet count ≥ 100,000/µL;

3. Total bilirubin ≤ 1.5 × ULN or ≤ 3.0 × ULN for subjects with hereditary benign
hyperbilirubinemia;

4. AST (SGOT) ≤ 3 × ULN (≤ 5 × ULN if liver metastases are present);

5. ALT (SGPT) ≤ 3 × ULN (≤ 5 × ULN if liver metastases are present);

6. Serum creatinine ≤ 1.5 mg/dL or a measured creatinine clearance ³ 60 mL/min
according to Cockcroft-Gault formula

4. Left ventricular ejection fraction informed (LVEF) ≥ 55%;

5. Ability to swallow and retain oral medications;

6. Negative serum beta-human Chorionic Gonadotropin (β-hCG) test in women of childbearing
potential (WOCBP); Note, subject must agree to use dual barrier contraceptive methods;
and

7. Willing and able to provide written informed consent and comply with the requirements
of the study;

8. Phase 1a Dose Escalation only - Histologically confirmed advanced solid tumor for
which standard therapy does not exist or is no longer effective

9. Food Effect Stage - willing and able to ingest a standard meal

10. Phase 1b All Expansion Cohorts - Evidence of measurable disease per RECIST, v1.1.
Measurable disease is defined as a lesion that can be accurately measured in at least
1 dimension (longest diameter to be recorded) with a minimum size of 10 mm by computed
tomography (CT) scan;

11. Phase 1b All Expansion Cohorts - Prior treatment with embolization or ablative
therapies is allowed if measurable disease remains outside of the treated area or if
there is definitive progression in the treated lesions. There is no limit on the
number of prior procedures;

12. Phase 1b Dose Expansion RAS Mutated mCRC Arm only - Histologically confirmed
colorectal cancer with a K-RAS or N-RAS mutation in exons 2,3 and 4 that is metastatic
or unresectable;

13. Phase 1b Dose Expansion RAS Mutated mCRC Arm only - At least 2 prior systemic
therapies for the treatment of metastatic colorectal cancer. Neo-adjuvant and adjuvant
therapies may not be counted as part of the prior therapy requirements. At least 7
subjects should be naïve to treatment with regorafenib;

14. Phase 1b Optional Dose Expansion Advanced RCC Arm only - Histologically confirmed
metastatic renal cell carcinoma;

15. Phase 1b Optional Dose Expansion Advanced RCC Arm only - Must have received 2 prior
therapies for metastatic RCC, including a vascular endothelial growth factor receptor
(VEGFR) tyrosine kinase inhibitor (TKI) and an immune checkpoint inhibitor (ie
anti-PD-1) (if approved and available for commercial use in the local country). At
least 7 subjects should be naïve to treatment with prior inhibitors of mammalian
target of rapamycin (mTOR) (eg. everolimus);

16. Phase 1b Optional Dose Expansion pNET Arm only - Histologically confirmed low-grade or
intermediate-grade, unresectable or metastatic pNET tumor for which standard therapy
does not exist or is no longer effective. Functional and non-functional tumors can be
included;

17. Phase 1b Optional Dose Expansion RAS-MAPK Pathway Mutation Arm only - Histologically
confirmed malignancy with a RAS-MAPK pathway mutation that is metastatic or
unresectable and for which standard therapy does not exist or is no longer effective.
At least 10 subjects with non-small cell lung cancer (NSCLC) are to be enrolled in
this arm.

Exclusion Criteria - All Phases

1. Any prior treatment (with the exception of somatostatin analogues, which are allowed
before and during the study in pNET subjects at the investigator discretion in pNET
subjects) such as chemotherapy, immunomodulatory drug therapy, anti-neoplastic
hormonal therapy (unless dose has been stable for 3 months prior to Baseline and will
remain stable during the study), immunosuppressive therapy, or corticosteroids (unless
administered to prevent contrast material reactions during radiographic procedures)
received within the past 28 days or 5 half-lives, whichever is shorter;

2. Presence of an acute or chronic toxicity resulting from prior chemotherapy, with the
exception of alopecia, that has not resolved to ≤ grade 1, as determined by NCI CTCAE
v 4.0 (http://evs.nci.nih.gov/ftp1/CTCAE/About.html);

3. Received radiotherapy within the last 21 days (limited palliative radiation is allowed
if ≥ 14 days prior);

4. Subjects with primary brain tumors or known central nervous system (CNS) metastases;

5. Major surgery < 28 days from the start of treatment (major surgery is defined as a
procedure requiring general anesthesia);

6. Minor surgery <14 days from the start of treatment (insertion of a vascular access
device is not considered major or minor surgery);

7. Active infection requiring systemic therapy;

8. Known to be human immunodeficiency virus (HIV) positive or have an acquired
immunodeficiency syndrome-related illness;

9. Uncontrolled congestive heart failure, angina, myocardial infarction, cerebrovascular
accident, coronary/peripheral artery bypass graft surgery, transient ischemic attack,
or pulmonary embolism within 3 months prior to initiation of study drug;

10. History of or ongoing cardiac dysrhythmias requiring treatment, atrial fibrillation of
any grade, or persistent prolongation of the QTc (Fridericia) interval to > 450 msec
for males or > 470 msec for females;

11. History of esophageal bleeding due to varices;

12. Gastrointestinal disease that may interfere with the absorption of orally-administered
drugs;

13. History of inflammatory bowel disease or other illness resulting in chronic diarrhea;

14. Known achlorhydria or history of gastrointestinal surgery that could reduce the
acidity of the stomach;

15. Acute pancreatitis or cholecystitis within 6 months prior to Baseline;

16. Cirrhosis with severe liver dysfunction (Child-Pugh Class B or C);

17. Previous or concomitant malignancy, except for basal-cell or squamous cell carcinoma
of the skin or carcinoma-in-situ of the uterine cervix. Subjects with other
malignancies are eligible if they have remained disease free for at least 2 years
prior to study entry;

18. Any severe, acute, or chronic medical or psychiatric condition, or laboratory
abnormality that may increase the risk associated with study participation or study
drug administration, may interfere with the informed consent process and/or with
compliance with the requirements of the study, or may interfere with the
interpretation of the study results and, in the Investigator's opinion, would make the
subject inappropriate for entry into this study;

19. Use of any investigational agents within 28 days or 5 half-lives (whichever is
shorter) prior to Baseline;

20. A condition that is expected to require concomitant use of any medication listed as
prohibited while on study;

21. Pregnant or lactating female;

22. Women of childbearing potential, or men who partner with a woman of childbearing
potential, unless they agree to use dual barrier contraceptive methods which, in the
Investigator's opinion, are effective and adequate for that subject's circumstances
while on study drug and for 3 months afterward;

23. Grade 3 or 4 eye disorder at study entry, unless stable and longstanding (>3 months)
and unlikely to interfere with protocol-required ophthalmology assessments;

24. Phase 1b Optional Dose Expansion pNET Arm only - Poorly differentiated pNET;

25. Phase 1b Optional Dose Expansion RAS-MAPK Pathway Mutation Arm only - Subjects with
primary pancreatic cancer or primary RAS mutated colorectal cancer.