Clinical Trial of HIV Vaccine Combinations in Healthy Men and Women

Human Immunodeficiency Virus Clinical Trial

— Ad4HIV  

Official title:

A Phase I Single-Blind Randomised Trial Investigating Immunisation Strategies Using Ad4-EnvCN54, MVA-CN54 and CN54gp140/MPLA Combinations in Order to Maximise Antibody Responses to Human Immunodeficiency Virus

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03408262
• Other study ID #: Ad4HIV
• Status: Completed
• Phase: Phase 1
• Start date: October 6, 2017
• Est. completion date: February 10, 2020

Study information

• Verified date: February 2020
• Source: Imperial College London
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a randomised two-part Phase I study which will explore the impact of different boosting options (MVA-CN54 and recombinant CN54gp140 protein) for oral Adenovirus serotype 4 vector prime expressing HIV-1 CN54 envelope (Ad4-EnvCN54) designed to optimize systemic and mucosal antibody responses.

Part 1 is exploratory and designed to select conditions capable of promoting enhanced systemic and mucosal B cell responses in a limited number of participants. Part 2 is dependent upon Part 1 and is designed to study groups selected on performance in part 1 in an expanded number of subjects. Data from both stages will be combined for safety and immunological analyses.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 68
• Est. completion date: February 10, 2020
• Est. primary completion date: February 10, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

1. Men and women aged between 18 and 50 years on the day of screening

2. BMI between 18-30

3. Seronegative for Adenovirus 4 serum neutralising antibodies

4. Available for follow-up for the duration of the study

5. Willing and able to give written informed consent

6. At low risk of HIV infection and willing to remain so for the duration of the study defined as:

• no history of injecting drug use in the previous ten years

• no gonorrhoea or syphilis in the last six months

• no high risk partner (e.g. injecting drug use, HIV positive partner) either currently or within the past six months

• no unprotected anal or vaginal intercourse in the last six months, outside a relationship with a regular partner known to be HIV negative

7. Willing to undergo HIV testing

8. Willing to undergo a STI screen for chlamydia, gonorrhoea and syphilis

9. Must agree to require male sexual partner to use condoms, from at least 14 days before the first vaccination until at least 4 months after the last

10. If heterosexually active female capable of becoming pregnant, must (in addition to requiring male partner to use condoms) agree to use hormonal contraception, or to complete abstinence, from at least 30 days before the first vaccination until at least 4 months after the last. [Note: Acceptable hormonal contraception is combined (estrogen and progestogen containing) or progestogen-only hormonal contraception associated with inhibition of ovulation. Complete abstinence can be used, when in line with the preferred and usual lifestyle of the subject. Periodic abstinence (calendar, symptothermal, post-ovulation methods), withdrawal (coitus interruptus), spermicides only, lactational amenorrhoea method, and IUD/IUS are not acceptable methods of contraception.]

11. If sexually active male, must agree to use condoms from the day of first vaccination until at least 4 months after the last. [Note: Additional use of an effective method of contraception is recommended for any non-pregnant female partner over the same period.]

12. Agree to abstain from donating blood, eggs or sperm from the day of first vaccination until at least 3 months after the end of their participation in the trial

13. Registered with a GP for at least the past month

14. Entered and clearance obtained from The Overvolunteering Prevention System (TOPS) database

Exclusion Criteria:

1. Are pregnant or breast feeding, or living with anyone under the age of 5 years old or over 75 years old

2. Have close contact with an immunocompromised individual thought to be at clinical risk from Adenovirus infection

3. Clinically relevant abnormality on history or examination including:

1. Liver disease with inadequate hepatic function

2. Any skin condition which may interfere with the trial assessment of the injection sites

3. Haematological, metabolic, gastrointestinal or cardio-pulmonary disorders

4. Uncontrolled infection; autoimmune disease, immunodeficiency

4. Known hypersensitivity to any component of the vaccine formulations used in this trial, or have severe or multiple allergies to drugs or pharmaceutical agents

5. History of severe local or general reaction to vaccination defined as

• Local: extensive, indurated redness and swelling involving most of the antero-lateral thigh or the arm, not resolving within 72 hours

• General: fever =39.5oC within 48 hours; anaphylaxis; bronchospasm; laryngeal oedema; collapse; convulsions or encephalopathy within 72 hours

6. Receipt of live attenuated vaccine within 60 days or other vaccine within 30 days of enrolment

7. Receipt of an experimental vaccines containing HIV antigens, Ad4 and MVA-C products at any time in the past

8. Receipt of blood products or immunoglobin within 4 months of screening, or drugs that suppress the immune system, such as steroids (including inhaled steroids, excluding topical steroids unless applied to the upper arm), in the preceding 3 months

9. Participating in another trial of a medicinal product, completed less than 30 days prior to enrolment

10. HIV 1 or 2 positive or indeterminate on screening

11. Positive for antibodies to hepatitis B surface antigen, hepatitis C antibody or serology indicating active syphilis requiring treatment

12. Clinically significant positive reaction in antinuclear antibody screen or clinically significant immunoglobulin (IgA, IgG or IgM) values

13. Grade 1 or above clinically significant routine laboratory parameters

14. Unable to read and/or speak English to a fluency level adequate for the full comprehension of procedures required in participation and consent

15. Women with a history of toxic shock syndrome

16. Women using an intrauterine device for contraception (as incompatible with softcup sampling)

17. Any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data

18. Unlikely to comply with protocol

Related Conditions & MeSH terms

• Acquired Immunodeficiency Syndrome
• HIV Infections
• Human Immunodeficiency Virus
• Immunologic Deficiency Syndromes

Intervention

Biological:
• Ad4-EnvCN54
Live, replication-competent adenovirus 4 vector, engineered to express the envelope glycoprotein of HIV-1 isolate 97CN54
• MVA-CN54
Live, non-replicating modified vaccinia Ankara vector, engineered to express the envelope glycoprotein of HIV-1 isolate 97CN54
• CN54gp140/MPLA
Recombinant glycoprotein of HIV-1 isolate 97CN54, with liposomal monophosphoryl lipid A adjuvant

Locations

Country	Name	City	State
United Kingdom	NIHR Imperial Clinical Research Facility	London

Sponsors (1)

Lead Sponsor	Collaborator
Imperial College London

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mucosal antigen-specific antibodies measured by binding ELISA	Frequency of mucosal binding antibodies to HIV CN54gp140 antigen	At two weeks after the final immunisation
Primary	Adverse events	Frequency of adverse events	Up to twenty-four weeks after the final immunisation
Secondary	Serum and mucosal antigen-specific antibodies measured by binding ELISA	Frequency of serum and mucosal binding antibodies to HIV CN54gp140 antigen	Up to twenty-four weeks after the final immunisation