VXM01 Phase I Study in Patients With Metastatic Colorectal Cancer With Liver Metastasis

NCT ID: NCT02718430

Last Updated: 2018-10-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 6 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-02-29
• Study Completion Date: 2018-03-31

Brief Summary

Phase I study in patients with metastatic colorectal cancer with liver metastasis under second or third line therapy to examine safety, efficacy, and immune biomarkers after treatment with VXM01

Conditions

Colorectal Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

VXM01

VXM01 10E6 or 10E7 CFU

Group Type: EXPERIMENTAL

VXM01

Intervention Type: DRUG

Oral immunotherapy targeting VEGFR2

Interventions

VXM01

Oral immunotherapy targeting VEGFR2

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Informed consent, including liver metastasis biopsy, signed and dated

2. Histologically or cytologically confirmed colorectal cancer, excluding primary tumors of appendiceal origin (participants are eligible to enroll irrespective of Kirsten rat sarcoma viral oncogene homolog (KRAS) mutation status)

3. Male or female patients who must be post-menopausal for at least 2 years or surgically sterile.

4. Confirmed metastatic colorectal cancer (Stage IV)

5. Presence of non-resectable liver metastasis

• Accessibility of liver metastasis appropriate for biopsy sampling
• Adequate coagulation parameters including platelet count ≥100,000/mm3
• Absence of concomitant medication which could represent a contraindication for biopsy (e.g., anti-platelet drugs including aspirin, ticlopidine, clopidogrel, IIb/IIIa receptor antagonists, non-steroidal anti-inflammatory drugs [NSAIDs], and vitamin K antagonist anticoagulants)

6. The participant has received first-line irinotecan- or oxaliplatin-based therapy without or in combination with a targeted antibody for metastatic disease and a) Experienced radiographic disease progression during first-line therapy, or b) Experienced radiographic disease progression ≤ 6 months after the last dose of first-line therapy, or c) Discontinued part or all of first-line therapy due to toxicity and experienced radiographic disease progression ≤ 6 months after the last dose of first-line therapy

7. Receipt of no more than 3 prior systemic therapy regimen for metastatic disease

8. Measurable or non-measurable disease based on the Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST v. 1.1)

9. Eastern Cooperative Oncology Group (ECOG) performance status 0-2

10. Life expectancy > 3 months

11. Adequate renal, hepatic, and bone marrow function

12. Leukocytes ≥4.0 x 109 / L

13. Absolute neutrophil count (ANC) > 1,500/mm3

14. Platelet count ≥ 100,000/mm3

15. Hemoglobin ≥ 9 g/dL (can be post-transfusion)

16. International normalized ratio (INR) ≤ 1.5

17. Activated partial thromboplastin time (aPTT) ≤ 1.5 times upper limit of normal (ULN)

18. Bilirubin ≤ 1.5 times ULN

19. ALT and AST ≤ 2.5 times ULN

20. Creatinine ≤ 2.0 mg/dL

21. Proteinuria ≤ 1+ by urine dipstick OR ≤ 1 g by 24-hour urine collection

22. Patients who are able to understand the nature and purpose of the study including possible risks, willing to comply with the requirements, and to provide their written informed consent to participate in the study

Exclusion Criteria

1. Concomitant treatment with anti-angiogenic therapy before progression of disease

2. Treatment in any other clinical trial within 30 days before screening.

3. Gastric bypass

4. Ileostoma

5. Other anatomical change of the gastrointestinal tract, interfering with gastrointestinal passage, except colostoma or colon bypass

6. Untreated CNS metastases. Participants with treated brain metastases are eligible if they are clinically stable with regard to neurologic function, off steroids after cranial irradiation ending at least 2 weeks prior to randomization, or after surgical resection performed at least 28 days prior to randomization. No evidence of Grade greater than or equal to 1 CNS hemorrhage based on pretreatment Magnetic Resonance Imaging (MRI) or intravenous (IV) contrast CT scan

7. Significant traumatic injury or surgery within the past 4 weeks

8. Cerebrovascular accident, transient ischemic attack, or subarachnoid hemorrhage within the past 6 months

9. Other malignancies within the past 5 years except for adequately treated carcinoma in situ of the cervix, and/or basal cell skin cancer, and/or early endometrial carcinoma

10. Pre-existing sensory or motor neuropathy ≥ grade 2

11. History or evidence of CNS disease (e.g., uncontrolled seizures) by neurological examination unless adequately treated with standard medical therapy

12. History or evidence of thrombotic or hemorrhagic disorders, including intracranial hemorrhage

13. Uncontrolled hypertension (i.e., blood pressure > 160/100 mm Hg)

14. Clinically significant cardiovascular disease, including any of the following:

• Myocardial infarction or unstable angina within the past 6 months
• New York Heart Association class III-IV congestive heart failure
• Poorly controlled cardiac arrhythmia despite medication, except rate controlled atrial fibrillation

15. Peripheral vascular disease ≥ grade 3 (i.e., symptomatic and interfering with activities of daily living requiring repair or revision)

16. Positive for anti-typhoid IgG/IgM antibodies according to the onsite test on Day 0

17. Hemoptysis within 6 months before randomization

18. Esophageal varices

19. Upper or lower gastrointestinal bleeding within 6 months before randomization

20. Non-healing wound, incomplete wound healing, bone fracture or any history of gastrointestinal ulcers within three years before inclusion, or positive gastroscopy within 3 months before inclusion

21. Gastrointestinal fistula

22. Thrombolysis therapy within 4 weeks before randomization

23. Presence of any acute or chronic systemic infection

24. Major surgical procedures, or open biopsy within 4 weeks before randomization

25. Chronic concurrent therapy within 2 weeks before and during the initial treatment period (Day 1 to Day 7):

• Corticosteroids (except steroids for adrenal failure or emesis prophylaxis up to 4 mg daily dose) or immunosuppressive agents
• Antibiotics
• Bevacizumab or any other anti-angiogenic treatment

26. Known multi-drug resistant gram-negative bacteria

27. History of other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that might affect the interpretation of the study results or render the patient at high risk for treatment complications

28. Women of childbearing potential

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Vaximm GmbH

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Carsten Gruellich, MD

Role: PRINCIPAL_INVESTIGATOR

National Center of Tumor Diseases Heidelberg

Locations

National Center of Tumor Diseases

Heidelberg, , Germany

Countries

Germany

Other Identifiers

VXM01-03-DE

Identifier Type: -

Identifier Source: org_study_id