A Study of the Intratumoural Administration of CAVATAK to Head and Neck Cancer Patients (VLA-X06)

NCT ID: NCT00832559

Last Updated: 2019-07-19

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 4 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-01-27
• Study Completion Date: 2011-07-28

Brief Summary

This study is designed to assess the safety and initial indications of efficacy resulting from multiple doses of CAVATAK injected directly into solid tumours of the Head and Neck that have been confirmed to express ICAM-1 and DAF.

CAVATAK (Coxsackievirus A21) is a naturally occurring common cold virus that preclinical research indicates can preferentially infect and kill cancer cells expressing the receptors ICAM-1 and/or DAF. This virus is known to cause self limiting upper respiratory infections and has been used previously to challenge therapies against the common cold. The virus is not generically modified.

The study proposes to administer CAVATAK to three cohorts each of three patients. The first cohort will receive a single dose, the second cohort will receive three doses, and the final cohort will receive six doses. There will a 48 hour interval between repeated doses.

The primary objective of the study is to determine the safety and efficacy of CVA21 given by intratumoural injection in the treatment of recurrent, unresectable squamous cell carcinoma of the head and neck by measuring primary and field tumour status and adverse effects.

Secondary objectives of the study are:

1. Indirect measurements of efficacy by measuring appropriate biomarkers in serum and tumour biopsy samples for viral replication, induction of apoptosis and anti-tumour immune responses.

2. To determine the time course of potential primary and secondary viraemia.

3. To characterise the time course of the anti-CVA21 antibody response after administration of CVA21

Conditions

Head and Neck Cancer

Study Design

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

Study Groups

CVA21

CVA21

Group Type: EXPERIMENTAL

CVA21

Intervention Type: BIOLOGICAL

1, 3 or 6 doses of CAVATAK (10\^9 TCID50) at 48 hour intervals.

Interventions

CVA21

1, 3 or 6 doses of CAVATAK (10\^9 TCID50) at 48 hour intervals.

Intervention Type: BIOLOGICAL

Other Intervention Names

CAVATAK; Coxsackievirus A21

Eligibility Criteria

Inclusion Criteria

1. Patients who are willing and able to provide written informed consent to participate in the study.

2. Patients with histologically confirmed metastatic or recurrent squamous cell carcinoma of the head or neck currently documented as "progressive disease"

3. Head and neck cancer patients with at least one tumour mass where the tumour mass is accessible for intratumoural injection and can be measured at periodic intervals for tumour size using callipers and/or ultrasound.

4. All patients to have histologically confirmed squamous cell carcinoma of the head and neck (excluding nasopharyngeal) that had recurred or relapsed after surgery and/or radiotherapy and/or chemotherapy.

5. The longest diameter of the target injectable tumour being no greater than 6 cm or no less than 1 cm in the longest diameter.

6. The tumour mass to be intratumourally injected to be easily accessible for injection and amenable to measurement by physical examination and / or radiographically.

7. Patients to be 18 years or older

8. Absence of circulating antibodies to CVA21 (titre < 1:16).

9. Adequate haematological, hepatic and renal function, defined as:

ANC > 1.5 x 109/L, platelets > 100 x 109/L Bilirubin < 20µmol/L, AST < 2.5 times the upper limit of normal Calculated creatinine clearance > 30 mL/minute

Adequate immunologic function, defined as:

Serum IgG > 5g/L T cell subsets within normal limits

10. Fertile males and females must agree to the use of an adequate form of contraception. Hormonal contraceptives should be supplemented with an additional barrier method. Negative pregnancy test is required in female patients of child-bearing potential.

Exclusion Criteria

1. Patients receiving radiotherapy to the proposed injected tumour or radiotherapy within the last 3 weeks

2. Performance status > 1 on the ECOG scale

3. Life expectancy < 3 months.

4. Pregnancy or breastfeeding.

5. Primary or secondary immunodeficiency, including immunosuppressive disease, and immunosuppressive doses of corticosteroids (e.g. prednisolone > 7.5mg per day) or other immunosuppressive medications including cyclosporine, azathioprine, interferons, within the past 4 weeks.

6. Positive serology for HIV, Hepatitis B or Hepatitis C.

7. Splenectomy.

8. Presence of uncontrolled infection.

9. Any uncontrolled medical condition that in the opinion of the Investigator is likely to place the patient at unacceptable risk during the study or reduce their ability to complete the study

10. Participation in another study requiring administration of an investigational drug or biological agent within the last 4 weeks

11. Known allergy to treatment medication or its excipients

12. Tumours to be injected lying in mucosal regions or close to an airway, major blood vessel or spinal cord that, in the opinion of the Investigators, could cause occlusion or compression in the case of tumour swelling or erosion into a major vessel in the case of necrosis

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

Sponsors

Viralytics

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Stephen Ackland, MBBS FRACP

Role: PRINCIPAL_INVESTIGATOR

Principal Investigator

Locations

St Vincents Hospital

Darlinghurst, New South Wales, Australia

Calvary Mater Newcastle Hospital

Newcastle, New South Wales, Australia

Monash Medical Centre

Clayton, Victoria, Australia

Countries

Australia

Other Identifiers

VLA-X06/PSX-X06

Identifier Type: OTHER

Identifier Source: secondary_id

V937-005

Identifier Type: -

Identifier Source: org_study_id