Dose-Escalation Study on Safety and Immunogenicity of VPM1002 in Comparison With BCG in Healthy Male Volunteers

Healthy Clinical Trial

Official title:

Phase I Open Label, Randomized, Controlled, Dose-Escalation Study to Evaluate Safety and Immunogenicity of VPM1002 in Comparison With BCG in Healthy Male Volunteers Stratified for History of BCG-Vaccination

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00749034
• Other study ID #: VPM1002-GE-1.01TB
• Status: Completed
• Phase: Phase 1
• First received: September 5, 2008
• Last updated: May 19, 2010
• Start date: September 2008
• Est. completion date: December 2009

Study information

• Verified date: April 2010
• Source: Vakzine Projekt Management GmbH
• Contact: n/a
• Is FDA regulated: No
• Health authority: Germany: Paul-Ehrlich-Institut
• Study type: Interventional

Clinical Trial Summary

Goal of VPM is the development of a recombinant urease C-deficient listeriolysin expressing BCG vaccine strain (VPM1002) as a safe, well tolerated and efficacious vaccine against TB for residents in endemic areas and persons at risk in non-endemic areas. The new live vaccine VPM1002 should be at least as potent as the currently used BCG vaccine and should cause fewer side effects (Kaufmann, 2007; Grode et al., 2005). It is formulated as lyophilised bacteria to be resuspended before intradermal injection. First application of VPM1002 in human male volunteers will evaluate its safety, local and systemic tolerability as well as its immunogenicity. The study has a dose-escalating sequential design with comparison to commercially available BCG. 80 volunteers in Germany will randomly be allocated to 4 groups each with 20 volunteers stratified for their history of BCG-vaccination.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: December 2009
• Est. primary completion date: December 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Male volunteers 18 to 55 years of age.

2. Healthy (medical history, physical examination, vital signs, ECG and laboratory tests at screening).

3. No signs of active or latent tuberculosis infection.

4. BMI of 19 - 30 kg/m2.

5. Subjects must be able and willing to comply with the study protocol, available and willing to complete all study measurements and have signed an Informed Consent form approved by the Ethics Committee.

6. Intention not to travel to endemic regions for tuberculosis (such as Africa, Asia, former USSR) and reachable by phone during the whole study period (6 months).

7. Negative test for HIV1 and HIV2, hepatitis B surface antigen and antibody to hepatitis C virus .

8. No anamnestic evidence for a primary or secondary immunodeficiency.

9. No skin eczema lesion at the intended injection site.

10. No anamnestic predisposition for scarring badly or for keloid formation.

11. No other vaccination during eight weeks before and during the follow-up period of the current study. If a vaccination is necessary during this period, the volunteer will be withdrawn from the study.

12. No participation in another clinical trial within 3 months before study vaccination and the 6 months of the current study.

13. Able and willing to abstain from physical exercise 24 hours before screening examination, and from 24 hours before admission until discharge from the clinic.

14. No blood donation for non study-related purposes during the entire duration of the study.

15. normal sonographic liver imaging

Exclusion Criteria:

For the group of volunteers who were vaccinated with a BCG vaccine:

• Tuberculin-PPD-in-vivo-test equal or more than 10 mm at baseline

For the group of naive volunteers:

• Tuberculin-PPD-in-vivo-Test equal or more than 1 mm at baseline

For all volunteers

1. systemic disorders which could interfere with the interpretation of the study results or compromise the health of the volunteers.

2. BCG-vaccination during 10 years before study vaccination.

3. Acute fever or fever in the last 7 days before dosing.

4. Any malignant condition.

5. Concomitant treatment with medication that may affect immune function during 3 months before study vaccination and the 6 months of current study.

6. Treatment with blood products or Immunoglobulins in the past 6 months up to end of study.

7. Any clinically significant laboratory abnormalities on screened blood samples.

8. A history of drug or alcohol abuse.

9. History of anaphylaxis or severe allergic reactions.

10. Positive test for drugs of abuse on urine testing at screening or admission.

11. Known allergies to any component of the investigational or reference product or known history of severe skin reaction against the Tuberculin test.

12. Professional or regular contact with life animals for food production.

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

• Healthy
• Tuberculosis

Intervention

Biological:
• VPM1002
live vaccine
• BCG
commercially available live vaccine BCG

Locations

Country	Name	City	State
Germany	Focus Clinical Drug Development GmbH	Neuss

Sponsors (1)

Lead Sponsor	Collaborator
Vakzine Projekt Management GmbH

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety: physical examination, vital signs, ECG, liver sonography, chest X-ray, laboratory safety parameters (including haematology, coagulation, clinical chemistry and urinalysis), tolerability, recording of concomitant medication and adverse events		days -1, 1, 2, 3, 5, 11, 29, 57 and month 6	Yes
Secondary	Immunogenicity: LST for PPD with subsequent IFN-gamma specific ELISA on supernatants of PBMC		baseline, days 29, 57, month 6	No
Secondary	Immunogenicity: ELISPOT for the number of IFN-gamma secreting PBMC after stimulation with PPD		baseline, days 29, 57, month 6	No
Secondary	Immunogenicity: whole blood stimulated with PPD and measuring IFN-gamma in the plasma by ELISA		baseline, days 29, 57, month 6	No
Secondary	ICS for IFN-gamma, TNF-alpha and IL-2 in CD4+ and CD8+ lymphocytes upon stimulation with PPD		baseline, days 29, 57 and month 6	No
Secondary	Immunogenicity: ICS with other triple combinations of markers in CD4+ and CD8+ lymphocytes upon stimulation with PPD		baseline, days 29, 57 and month 6	No
Secondary	Immunogenicity: TB85B as recall antigen for ELISA, ELISPOT, WBA and ICS		baseline, days 29, 57 and month 6	No
Secondary	Immunogenicity: serum antibodies against PPD or AG85B		baseline, days 29, 57 and month 6	No

External Links

•   Background Information on VPM1002
•   Press Release on First Application of VPM1002