Lung Cancer Clinical Trial

CVA21 and Pembrolizumab in NSCLC & Bladder Cancer (VLA-009 STORM/ KEYNOTE-200)

Summary

The purpose of this trial is to assess the ability of CVA21, either alone (Part A) or in combination with pembrolizumab (Part B), to reach and to replicate in existing tumors (while sparing normal cells) and to establish a safe multi-dose schedule of the virus for the treatment of solid tumors where enhanced expression of ICAM-1 and/ or DAF receptor occurs.

This trial consists of 2 sequential parts: VLA-009 (Part A) conducted only in the UK and employed CVA21 as a monotherapy in NSCLC, castrate-resistant prostate cancer, melanoma and bladder cancer. VLA-009 (Part B) conducted in the US, AUS and UK employs CVA21 with pembrolizumab in NSCLC and bladder cancer.

Both VLA-009A and VLA-009B are open-label, multi-center, ascending dose escalation (3+3 design) dose-finding and signal-seeking studies.

Part A of the study is now complete and closed to enrolment. Part B is currently enrolling.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically-confirmed (1) NSCLC, (2) bladder cancer, (3) castrate-resistant prostate cancer which are metastatic, or (4) stage 3C or stage 4 melanoma.
VLA009A: Locally advanced and/or metastatic disease for which curative surgery and/or radiation therapy is not possible and judged not to be a candidate for the current standard of care treatment. VLA009B: locally advanced and/or metastatic disease and judged to be a candidate for pembrolizumab to be used in combination with CVA21.
All subjects in Cohort 3 or Phase 2 dose (P2D) must have a lesion accessible for FNA or core or open biopsy on day 8 of the first treatment cycle.
No CVA21 neutralising antibody (≤ 1:16)
Measurable or evaluable disease

Exclusion Criteria:

Second primary malignancy within the past 2 years (except non-melanoma skin cancer, in situ carcinoma of the cervix, breast cancer)
Concurrent immunosuppressive therapy and no known immunosuppressive disease other than primary tumour

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

85

Study ID:

NCT02043665

Recruitment Status:

Completed

Sponsor:

Viralytics

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 18 Locations for this study

See Locations Near You

John Wayne Cancer Institute
Santa Monica California, 90404, United States
University of Miami
Coral Gables Florida, 33146, United States
Advocate Health
Niles Illinois, 60714, United States
Karmanos Cancer Institute
Detroit Michigan, 48201, United States
Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States
Providence Portland Medical Center
Portland Oregon, 97213, United States
Fox Chase Cancer Center
Philadelphia Pennsylvania, 19111, United States
UT Southwestern
Dallas Texas, 75390, United States
Huntsman Cancer Institute
Salt Lake City Utah, 84112, United States
Tasman Oncology Research
Southport Queensland, 4216, Australia
Monash Health
Clayton Victoria, 3168, Australia
St Vincent's Hospital, Melbourne
Fitzroy Victoria, 3065, Australia
Barwon Health
Geelong Victoria, 3220, Australia
Epworth HealthCare
Richmond Victoria, 3121, Australia
St John of God Healthcare
Subiaco Western Australia, 6008, Australia
Royal Marsden NHS Foundation Trust
Chelsea , SW3 6, United Kingdom
Royal Surrey County Hospital
Guildford , GU2 7, United Kingdom
St. James University Hospital
Leeds , LS9 7, United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

85

Study ID:

NCT02043665

Recruitment Status:

Completed

Sponsor:


Viralytics

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.