A Phase I Clinical Trial to Assess the Safety and Immunogenicity of HIV DNA-C CN54ENV Immunisations Administered Via the IM and ID Methods With and Without Electroporation Followed by Boosting With Recombinant HIV CN54gp140 in Healthy Male and Female Volunteers
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 28
- 试验地点
- 1
- 主要终点
- Primary Safety Endpoint
研究概览
简要总结
CUTHIVAC002 is a randomised Phase I study aimed at exploring the safety and immunogenicity of two different modes of delivery of a deoxyribonucleic acid (DNA) vaccine (DNA-C CN54ENV) via combined intramuscular and intradermal methods with and without electroporation, and boosted with recombinant HIV CN54gp140 administered by intradermal injection in healthy volunteers.
The aim of this study is to identify optimal DNA delivery conditions for promoting enhanced antibody responses to boosting with recombinant protein by the intradermal method.
详细描述
CUTHIVAC002 is a randomised Phase I study in healthy volunteers, aimed at exploring the safety and immunogenicity of two different modes of delivery of a deoxyribonucleic acid (DNA) HIV vaccine via combined intramuscular and intradermal methods with and without electroporation (EP), and boosted with recombinant HIV protein vaccine administered by intradermal injection without EP.
The aim of this study is to identify optimal DNA delivery conditions for promoting enhanced antibody responses to boosting with recombinant protein by the intradermal route. Healthy male and female volunteers aged 18 to 50 years old, who are at low risk of HIV infection, are to be recruited. The participants will be divided into 3 groups:
Group 1:
Participants will receive 1 x 0.15 ml (0.6 mg) DNA intradermal injections into the upper arm with EP and 1 x 0.5 ml (2 mg) intramuscular injection into the upper thigh without EP at Weeks 0, 4 & 8. And also 1 x 0.1 ml (50 μg) HIV recombinant protein by intradermal injection into the upper arm at Week 20 (final vaccination).
Group 2:
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Men and women aged between 18 and 50 years on the day of screening
- •BMI between 18-30
- •Available for follow-up for the duration of the study (~5 months from screening)
- •Willing and able to give written informed consent
- •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
- •Willing to undergo a HIV test
- •Willing to undergo a genital infection screen
- •Must agree to require male sexual partner to use condoms, from at least 14 days before the first vaccination until at least 14 days after the last
- •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 14 days before the first vaccination until at least 14 days after the last. [Note: Periodic abstinence (e.g. calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal, and IUD/IUS, are not acceptable methods of contraception.] If sexually active male, must agree to use condoms from the day of first vaccination until at least 14 days after the last. [Note: Additional use of an effective method of contraception is recommended for any non-pregnant female partner over the same period.]
- •Agree to abstain from donating blood for three months after the end of their participation in the trial, or longer if necessary
- •Registered with a GP for at least the past three months
- •Entered and clearance obtained from The Over-volunteering Prevention System (TOPS) database.
排除标准
- •Pregnant or lactating
- •History of cardiac arrhythmia or palpitations [e.g., supraventricular tachycardia, atrial fibrillation, frequent ectopy, or sinus bradycardia prior to study entry (sinus arrhythmia is not excluded)
- •History of syncope or fainting episodes within 1 year of study entry
- •History of grand-mal epilepsy, seizure disorder or any history of prior seizure
- •Individuals in which a skin-fold measurement (cutaneous and subcutaneous tissue) of the upper right or left thigh exceeds 40 mm
- •Clinically relevant abnormality on history or examination
- •Known hypersensitivity to any component of the vaccine formulations used in this trial, or have severe or multiple allergies to drugs or pharmaceutical agents
- •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 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
- •Receipt of live attenuated vaccine or HIV envelope components within 60 days or other vaccines within 14 days of enrolment
- •Receipt of an experimental vaccine containing HIV envelope components at any time in the past
- •Receipt of blood products or immunoglobulin within 4 months of screening
- •Participation in another trial of a medicinal product, completed less than 30 days prior to enrolment.
- •HIV 1 or 2 positive or indeterminate on screening.
- •Positive for hepatitis B surface antigen, hepatitis C antibody or serology indicating active syphilis requiring treatment
- •Grade 1 or above routine laboratory parameters. Hyperbilirubinaemia to be considered an exclusion criterion only when confirmed to be conjugated bilirubinaemia
- •Current use of any electronic stimulation device, such as cardiac demand pacemakers, automatic implantable cardiac defibrillator, nerve stimulators, or deep brain stimulators.
- •Presence of any surgical or traumatic metal implants at the sites of administration
- •Unable to read and speak English to a fluency level adequate for the full comprehension of procedures required in participation and consent.
- •Women with a history of toxic shock syndrome.
- •Women using an intrauterine device for contraception (as incompatible with softcup sampling)
- •Unlikely to comply with protocol.
研究组 & 干预措施
Group 1: ID/EP + IM
0.6 mg DNA-C CN54ENV, intradermally with electroporation, at Weeks 0, 4 and 8. 2 mg DNA-C CN54ENV, intramuscularly without electroporation, at Weeks 0, 4 and 8.
50 µg CN54gp140, intradermally without electroporation, at Week 20.
干预措施: DNA-C CN54ENV (Biological)
Group 1: ID/EP + IM
0.6 mg DNA-C CN54ENV, intradermally with electroporation, at Weeks 0, 4 and 8. 2 mg DNA-C CN54ENV, intramuscularly without electroporation, at Weeks 0, 4 and 8.
50 µg CN54gp140, intradermally without electroporation, at Week 20.
干预措施: CN54gp140 (Biological)
Group 1: ID/EP + IM
0.6 mg DNA-C CN54ENV, intradermally with electroporation, at Weeks 0, 4 and 8. 2 mg DNA-C CN54ENV, intramuscularly without electroporation, at Weeks 0, 4 and 8.
50 µg CN54gp140, intradermally without electroporation, at Week 20.
干预措施: Trigrid Delivery System - Intradermal (Device)
Group 2: ID + IM/EP
0.6 mg DNA-C CN54ENV, intradermally without electroporation, at Weeks 0, 4 and 8.
2 mg DNA-C CN54ENV, intramuscularly with electroporation, at Weeks 0, 4 and 8. 50 µg CN54gp140, intradermally without electroporation, at Week 20.
干预措施: DNA-C CN54ENV (Biological)
Group 2: ID + IM/EP
0.6 mg DNA-C CN54ENV, intradermally without electroporation, at Weeks 0, 4 and 8.
2 mg DNA-C CN54ENV, intramuscularly with electroporation, at Weeks 0, 4 and 8. 50 µg CN54gp140, intradermally without electroporation, at Week 20.
干预措施: CN54gp140 (Biological)
Group 2: ID + IM/EP
0.6 mg DNA-C CN54ENV, intradermally without electroporation, at Weeks 0, 4 and 8.
2 mg DNA-C CN54ENV, intramuscularly with electroporation, at Weeks 0, 4 and 8. 50 µg CN54gp140, intradermally without electroporation, at Week 20.
干预措施: Trigrid Delivery System - Intramuscular (Device)
Group 3: ID/EP + IM/EP
0.6 mg DNA-C CN54ENV, intradermally with electroporation, at Weeks 0, 4 and 8. 2 mg DNA-C CN54ENV, intramuscularly with electroporation, at Weeks 0, 4 and 8. 50 µg CN54gp140, intradermally without electroporation, at Week 20.
干预措施: DNA-C CN54ENV (Biological)
Group 3: ID/EP + IM/EP
0.6 mg DNA-C CN54ENV, intradermally with electroporation, at Weeks 0, 4 and 8. 2 mg DNA-C CN54ENV, intramuscularly with electroporation, at Weeks 0, 4 and 8. 50 µg CN54gp140, intradermally without electroporation, at Week 20.
干预措施: CN54gp140 (Biological)
Group 3: ID/EP + IM/EP
0.6 mg DNA-C CN54ENV, intradermally with electroporation, at Weeks 0, 4 and 8. 2 mg DNA-C CN54ENV, intramuscularly with electroporation, at Weeks 0, 4 and 8. 50 µg CN54gp140, intradermally without electroporation, at Week 20.
干预措施: Trigrid Delivery System - Intramuscular (Device)
Group 3: ID/EP + IM/EP
0.6 mg DNA-C CN54ENV, intradermally with electroporation, at Weeks 0, 4 and 8. 2 mg DNA-C CN54ENV, intramuscularly with electroporation, at Weeks 0, 4 and 8. 50 µg CN54gp140, intradermally without electroporation, at Week 20.
干预措施: Trigrid Delivery System - Intradermal (Device)
结局指标
主要结局
Primary Safety Endpoint
时间窗: From first dose until up to Week 22
Number of participants experiencing a Grade 3 or above solicited local, systemic or laboratory adverse event, or any grade of adverse event leading to a clinical decision to discontinue immunizations, or any grade of unsolicited adverse event with onset within 7 days of immunization
Primary Immunogenicity
时间窗: Week 22
Magnitude of antigen-specific systemic IgG antibody binding responses (ng/mL) to CN54gp140
次要结局
- Adverse Event Local to the Injection Sites, Starting Within 7 Days of Injection(7 days after injection)