RNActive® Rabies Vaccine (CV7201) in Healthy Adults

Rabies Clinical Trial

Official title:

Phase I Safety and Immunogenicity Trial of an Investigational RNActive® Rabies Vaccine (CV7201) in Healthy Adults

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02241135
• Other study ID #: CV-7201-102
• Secondary ID: 2013-002171-17
• Status: Completed
• Phase: Phase 1
• Start date: October 2013
• Est. completion date: February 8, 2018

Study information

• Verified date: May 2018
• Source: CureVac AG
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this trial is to assess the safety and immunogenicity of an investigational RNActive® rabies vaccine (CV7201) in healthy adults.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 101
• Est. completion date: February 8, 2018
• Est. primary completion date: February 8, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

1. Healthy male and female volunteers aged 18 to 40 years inclusive

2. Compliant with protocol procedures and available for clinical follow-up through the last planned visit (V9)

3. Physical examination and laboratory results without clinically significant findings

4. Body Mass Index (BMI) = 18.0 and = 32.0 kg/m2

5. Females: Negative human chorionic gonadotropin (HCG) pregnancy test (serum) for women presumed to be of reproductive potential on the day of enrolment

6. Females of childbearing potential must use acceptable methods of birth control during the trial and Follow-up period (from 6 weeks before the first administration of the test vaccine for the duration of the trial i.e., until the last planned visit (V9)). The following methods of birth control are acceptable when used consistently and correctly: established use of oral, injected or implanted hormonal methods of contraception; intrauterine devices (IUDs) or intrauterine systems (IUSs) with the exception of steel or copper wire; barrier methods of contraception (condom or occlusive cap [diaphragm or cervical/vault caps] with spermicidal foam/gel/film/cream/suppository); true abstinence (periodic abstinence [e.g., calendar, ovulation, symptothermal and postovulation methods] and withdrawal are not acceptable).

7. Males must use reliable forms of contraception (barrier method with spermicidal agent or true abstinence) and must refrain from sperm donation during the trial and Follow-up period i.e., until the last planned visit (V9).

Exclusion Criteria:

1. Use of any investigational or non-registered product (drug or vaccine) other than the trial vaccine within 4 weeks preceding the administration of the trial vaccine, or planned use during the trial period

2. Subject has received any other licensed vaccines within 4 weeks prior to the administration of the trial vaccine

3. Subject has received any investigational or licensed rabies vaccine previously

4. Intending to travel to regions/countries for which rabies vaccinations are recommended or where high risk of infections exists according to travel recommendations by the German Society of Tropical Medicine and International Health (DTG) during the trial and up to V9 (Day 91/120) Follow-up

5. Any treatment with immunosuppressants or other immune-modifying drugs within 6 months prior to the administration of the trial vaccine. The use of inhaled and nasal steroids, as well as topical steroids outside the vaccination area, will be permitted

6. Any medically diagnosed or suspected immunodeficient condition based on medical history and physical examination

7. History of autoimmune disease

8. Administration of immunoglobulins (Igs) and/or any blood products within the 3 months preceding the administration of the trial vaccine

9. Subject is taking chloroquine for malaria treatment or prophylaxis

10. Acute disease at the time of enrolment. Acute disease is defined as the presence of a moderate or severe illness or fever = 38 °C measured orally

11. Presence or evidence of significant acute or chronic, uncontrolled medical or psychiatric illness (subjects with uncomplicated chronic diagnoses stable and treated for = 3 months e.g., mild hypertension well-controlled with medication, may be enrolled - provided the condition and its therapy are known not to be associated with an immunocompromised state or an autoimmune disease

12. Major congenital defects

13. Known allergy to any component of the trial product i.e., protamine. This includes subjects with allergy to fish protein, diabetics with allergy to protamine-containing insulin, or post-vasectomy males

14. Known type I allergy to beta lactam antibiotics

15. Evidence of current alcohol or drug abuse

16. History of any neurological disorders or seizures, with the exception of febrile seizures during childhood

17. Seropositivity for human immunodeficiency virus (HIV), hepatitis B virus (HBV) (except in subjects previously vaccinated against HBV) or hepatitis C virus (HCV)

18. Foreseeable non-compliance with protocol as judged by the Investigator

19. For females: Pregnancy or lactation

20. History of any life-threatening anaphylactic reactions.

21. Subjects with impaired coagulation in whom an IM injection is contraindicated.

Related Conditions & MeSH terms

• Rabies

Intervention

Biological:
• CV7201 mRNA
CV7201 is composed of 1 RNActive® mRNA that encodes the rabies virus glycoprotein.

Locations

Country	Name	City	State
Germany	Abteilung für Infektions- und Tropenmedizin der Ludwig-Maximilians-Universität	Munich

Sponsors (1)

Lead Sponsor	Collaborator
CureVac AG

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence and severity of serious adverse events (SAEs)/adverse events (AEs) and local tolerability assessment of the vaccination site	The occurrence of AEs will be assessed by non-directive questioning of the subject at each visit. Further, AEs volunteered by the subject during or between visits - as subject diary card entries - or detected through observation, physical examination, laboratory test, or other assessments during the entire observation period, will be documented. Subjects will be instructed that they must immediately report any AEs, subjective complaints or objective changes in their well-being to the Investigator or the clinic personnel, regardless of the perceived relationship between the event and the test product. The Investigator is responsible for reporting all AEs in the eCRF that are observed or described by the subject, regardless of their relationship to the trial vaccine or their clinical significance.	up to 64 days after the last vaccination
Secondary	The lowest CV7201 dose to elicit rabies VNTs = 0.5 IE/ml	Rabies virus neutralizing titers (VNTs) measured in serum blood samples taken 14 days after the the last vaccination (Visit 8).	Rabies VNTs measured 14 days after the 3rd vaccination (Visit 8)
Secondary	Number of treatment discontinuation due to IMP-related AEs/SAEs	Number of subjects discontinued from treatment after the first or second vaccination due to vaccination-related reactions or AEs/SAEs.; Period for observation in order to decide on withdrawal of subjects from next vaccination starts with Visit 1 (day 0, first vaccination) and lasts until the day of the third scheduled vaccination (pre-vaccination examination).	up to 64 days after the last vaccination