Study of Safety and Tolerability of Intravenous CRS-100 in Adults With Carcinoma and Liver Metastases

Neoplasm Metastasis Clinical Trial

Official title:

Phase 1 Dose-Escalation Study of Safety and Tolerability of Intravenous CRS-100 in Adults With Carcinoma and Liver Metastases

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00327652
• Other study ID #: VAC05001
• Status: Completed
• Phase: Phase 1
• First received: May 17, 2006
• Last updated: April 22, 2008
• Start date: October 2006

Study information

• Verified date: April 2008
• Source: Anza Therapeutics, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This clinical trial evaluated the safety and tolerability of CRS-100, an investigational agent containing a live-attenuated strain of Listeria monocytogenes (Lm). CRS-100 is attenuated by genetic modification to limit cell to cell spread and invasion of liver cells. These attenuations result in decreased virulence of CRS-100 in mice but retain the ability of the investigational agent to stimulate immunity in test animals and generate anti-tumor activity in mice. The primary objective of this study was to determine the maximum tolerated dose (MTD) and to explore the safety profile of a single intravenous dose of CRS-100 in consenting volunteers. Immunological response to CRS-100 and tumor status of study participants were also measured. Participation in this first clinical trial with CRS-100 was restricted to adults with carcinoma refractory to standard treatment (or for whom no standard treatment is available) and who additionally had liver metastases.

Description:

Patients who consented to participate in the study were evaluated for eligibility according to their medical history, physical examination, blood testing, and computed tomography (CT) scan of thorax, abdomen, and pelvis. Those patients who qualified for the study received a single intravenous dose of CRS-100 on study day 1, after which they remained in the hospital for five days for safety monitoring of health status, including serial blood collections. Study participants returned for out-patient follow-up for further blood tests and additional monitoring of safety and immune response to CRS-100. At day 56, after administration of CRS-100, participants had a repeat CT scan to measure tumor size, and they were then discharged from the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 9
• Est. primary completion date: February 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria (abbreviated):

1. Documented carcinoma refractory to standard treatment (or for whom no standard treatment is available). Hepatocellular carcinoma (HCC) is not allowed.

2. Hepatic metastases

3. ECOG Performance Status of 0 or 1, or Karnofsky Performance Status (KPS) of 80% to 100%.

4. Adequate organ function as defined by clinical hematology and chemistry assays.

Exclusion Criteria (abbreviated):

1. Known central nervous system metastases.

2. History of allergic reactions attributed to sulfa or beta-lactam antibiotics.

3. Cardiac conditions associated with high- or moderate-risk of endocarditis.

4. Intra-arterial hepatic catheter, hepatic cirrhosis, or clinically relevant ascites.

5. Artificial (prosthetic) joint or other artificial implant or devices that cannot easily be removed.

6. Known coagulation disorder or recent thromboembolic event.

7. Use of immunosuppressive agent, chemotherapy, or radiation therapy within 28 days prior to CRS-100; bone marrow or stem cell transplant or a major organ allograft; autoimmune disease.

8. Current history of gallstones or kidney stones.

9. Infection with HIV, human t-lymphotropic virus type 1 (HTLV-1), hepatitis c virus (HCV), or hepatitis b virus (HBV).

10. Pregnant or lactating

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Carcinoma
• Liver Neoplasms
• Neoplasm Metastasis
• Neoplasms

Intervention

Drug:
• CRS-100
Live-attenuated Listeria monocytogenes

Locations

Country	Name	City	State
United States	Johns Hopkins University	Baltimore	Maryland
United States	Mary Crowley Medical Research Center	Dallas	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Anza Therapeutics, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dose-limiting toxicities (DLTs) for 7 days after dosing		7 days	Yes