Investigating Immunisation Strategies of DNA, MVA and CN54rgp140 Adjuvanted With GLA-AF to Maximise Antibody Responses (UKHVCSpoke003)
Status and phase
Conditions
Treatments
Study type
Funder types
Identifiers
Details and patient eligibility
About
UKHVC Spoke 003 is a randomised Phase I, two centre study which will explore the impact of shortening a vaccination regimen using deoxyribonucleic acid (DNA) (CN54ENV and ZM96GPN), Modified Vaccinia Ankara - C (MVA-C) and CN54rgp140 adjuvanted with glucopyranosyl lipid A adjuvant - aqueous form (GLA-AF). The study population will be 40 healthy male and female volunteers 18 to 45 years old who are at low risk of HIV infection are to be recruited.
Study participants will be immunised with trial immunogens:
- 8mg DNA: one plasmid encoding a gag-pol-nef polypeptide derived from the 96ZM651-8 clone and one plasmid encoding gp140 env derived from clade C 97CN54
- 1.108 TCID50 MVA-C (nominal titre) expressing the gag-pol-nef and gp120 env proteins derived from clade-C 97CN54
- 100ug CN54rgp140, a trimeric recombinant envelope protein derived from clade C 97CN54
- 5ug GLA-AF, an aqueous glucopyranosyl lipid A adjuvant
All immunisations will be administered by the intramuscular route (IM). CN54gp140 and GLA will be mixed together before administration, and immunogens will be delivered in combination regimens
Full description
This is a phase I study exploring the safety and potency of five HIV vaccines in healthy volunteers. The main aim is to see whether three of the five vaccines can be given together rather than one after the other, in five rather than seven sets of vaccinations and a course shortened by eight weeks. All volunteers will receive three injections of the first two vaccines (DNA plasmids) and half will be randomly assigned to receive two injections each of the second (MVA-C) and subsequent vaccines (CN54rgp140 mixed with GLA-AF) during the same visit or two injections of the MVA-C followed by two of CN54rgp140 mixed with GLA-AF.
The investigators are interested in ensuring that the vaccines are safe and also that the immune responses in the two groups of volunteers are similar. The three vaccines have all been shown to stimulate the immune response to specific parts of the HIV virus and none are infectious. The first vaccine consists of two DNA plasmids. When injected into muscle cells small parts of the HIV virus which are encoded by the DNA are produced and these are then recognised by the immune system. The second vaccine MVAC, is derived from vaccinia virus which has been modified so that it cannot divide. The virus (Modified Vaccinia Ankara (MVA)) actually expresses the same portions of HIV as the DNA and results in amplification of the responses seen. The third vaccine is a synthetically produced component of the HIV viral outer coat and it will be administered with an additive which has been shown to greatly enhance particular types of immune response which have recently been shown to play a role in protection against infection
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
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Man or woman aged between 18 and 45 years on the day of screening
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Available for follow-up for the duration of the study (up to ~10 months from enrolment)
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At low risk of HIV 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 intercourse in the last six months, outside a relationship with a regular partner known to be HIV negative
- no unprotected vaginal intercourse in the last six months outside a relationship with a regular known/presumed HIV negative partner
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Willing to undergo an HIV test
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Willing to undergo a genital infection screen if indicated by sexual history
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If heterosexually active female, using an effective method of contraception with partner other than an IUCD/IUS (combined oral contraceptive pill; injectable or implanted contraceptive; consistent record with condoms if using these; physiological or anatomical sterility in self or partner) from 14 days prior to the first vaccination until 4 months after the last, and willing to undergo urine pregnancy tests prior to each vaccination
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If heterosexually active male, using an effective method of contraception with their partner from the first day of vaccination until 4 months after the last vaccination
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Agree to abstain from donating blood for three months after the end of their participation in the trial, or longer if necessary
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Registered with a general practitioner (GP) for at least the past three months
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Satisfactory response received from GP before randomisation
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Willing and able to give written informed consent
Exclusion criteria
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Pregnant or lactating
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Presence of an IUCD (intrauterine contraceptive device)/IUS (intrauterine system)
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Clinically relevant abnormality on history or examination including
- history of grand-mal epilepsy, seizure disorder or any history of prior seizure
- severe eczema
- liver disease with inadequate hepatic function
- any skin condition which may interfere with the trial assessment on the injection site
- haematological, metabolic, gastrointestinal or cardio-pulmonary disorders
- uncontrolled infection; toxic shock syndrome; autoimmune disease, immunodeficiency or use of immunosuppressives in preceding 3 months
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Known hypersensitivity to any component of the vaccine formulations used in this trial, or have severe or multiple allergies to drugs or pharmaceutical agents
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History of severe local or general reaction to vaccination defined as
- local: extensive, indurated redness and swelling involving the major circumference of the arm, not resolving within 72 hours
- general: fever >= 39.5°C within 48 hours; anaphylaxis; bronchospasm; laryngeal oedema; collapse; convulsions or encephalopathy within 72 hours
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Receipt of live attenuated vaccine within 60 days or other vaccine within 14 days of enrolment
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Receipt of an experimental vaccine containing HIV antigens at any time in the past
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Receipt of blood products or immunoglobin within 4 months of screening
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Participation in another trial of a medicinal product, completed less than 30 days prior to enrolment
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HIV 1 or 2 positive or indeterminate on screening
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Positive for hepatitis B surface antigen, hepatitis C antibody or serology indicating active syphilis requiring treatment
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Grade 1 or above routine laboratory parameters. Hyperbilirubinaemia to be considered an exclusion criterion only when confirmed to be conjugated bilirubinaemia
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Unable to read and speak English to a fluency level adequate for the full comprehension of procedures required in participation and consent.
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Unlikely to comply with protocol
Trial design
Primary purpose
Allocation
Interventional model
Masking
40 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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