VRC 018: A Phase I Dose Escalation, Randomized, Open-Label Clinical Trial to Evaluate Dose, Safety, Tolerability and Immunogenicity of a HIV-1 Vaccine, VRC-HIVRGP096-00-VP, With Alum in Healthy Adults
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 16
- 试验地点
- 1
- 主要终点
- Number of Participants Reporting Local Reactogenicity Signs and Symptoms For 7 Days After Each Product Administration
研究概览
简要总结
Background:
HIV stands for human immunodeficiency virus, which is the virus that causes AIDS. There is currently no licensed vaccine to prevent HIV infection. Researchers want to test a vaccine called Trimer 4571 for the first time. It was made at the National Institutes of Health (NIH) and contains no HIV. The vaccine is mixed with a substance called alum and injected in the arm. Alum is included to boost the body's immune response to the vaccine. It has been used in licensed vaccines for over 60 years and has been found to be safe.
Objectives:
To see if the vaccine Trimer 4571 is safe, well-tolerated, and to study immune responses to it.
Eligibility:
Healthy adults ages 18-50 years
Design:
Participants were screened with a physical exam and blood tests. They agreed to not become pregnant and to avoid behavior that would put them at high-risk for HIV infection during the study.
Participants had about 15 study visits over about 9 months.
The first 6 participants received a low dose of the vaccine mixed with alum.
Once the low dose was deemed safe, 10 new participants were allocated to receive a higher dose.
All participants were randomly assigned to get the vaccine by injection in a muscle or under the skin.
All participants received a total of 3 vaccine injections over 20 weeks. Each visit where participants received the vaccine lasted about 5 hours. Participants were watched after each injection. Participants who were able to get pregnant would have a pregnancy test before each injection.
Participants received a thermometer and recorded their temperature and symptoms every day for 1 week after each injection. The injection site was checked for redness, swelling, or bruising.
At follow-up visits, participants had blood drawn and checked for health changes or problems. Follow up visits lasted about 1-2 hours.
详细描述
Design:
This is a Phase I, open-label, dose escalation study to evaluate the dose, safety, tolerability, and immunogenicity of VRC-HIVRGP096-00-VP (Trimer 4571) with aluminum hydroxide suspension (alum) as adjuvant in a three-injection regimen. The hypotheses were that the vaccine will be safe and tolerable and will induce detectable immune responses. The primary objective was to evaluate the safety and tolerability of the investigational vaccine at three doses administered with alum. Secondary objectives were to evaluate humoral and cellular immunogenicity of the investigational vaccine regimens.
Study Product:
VRC-HIVRGP096-00-VP (Trimer 4571) was developed by the Vaccine Research Center (VRC), National Institute of Allergy and Infectious Diseases (NIAID). The soluble HIV-1 envelope product consists of an HIV-1 envelope (Env) trimer variant, derived from clade A, strain BG505, with stabilizing mutations and engineered disulfide bonds, specifically recognized by broadly neutralizing antibodies and resists gp120 conformational change caused by CD4 binding. Injections were administered intramuscularly (IM) and subcutaneously (SC) in a 1 mL volume by needle and syringe. The product was provided at a 500 mcg/mL concentration in 3 mL glass vials filled to 1.2 +/- 0.10 mL. Adjuvant is an aluminum hydroxide suspension (alum) provided in a sterile, pyrogen-free suspension at a concentration of 5 mg/mL in 3 mL glass vials filled to 0.7 +/- 0.10 mL.
Participants:
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Sequential
- 主要目的
- Prevention
- 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
- •INCLUSION CRITERIA:
- •A participant must have met all of the following criteria:
- •Able and willing to complete the informed consent process.
- •18-50 years old, inclusive, on day of enrollment.
- •Available for clinic follow-up through the last study visit.
- •Able to provide proof of identity to the satisfaction of the study clinician completing the enrollment process.
- •Willing to donate blood for sample storage to be used for future research.
- •In good general health without clinically significant medical history.
- •Physical examination and laboratory results without clinically significant findings.
- •Body Mass Index (BMI) less than or equal to
- •Assessed as low risk for human immunodeficiency virus (HIV) acquisition by agreeing to discuss HIV infection risks, agreeing to risk reduction counseling, and agreeing to avoid behavior associated with high risk of HIV exposure through the end of study.
- •Screening laboratory values within 56 days prior to enrollment that met the following criteria:
- •Hemoglobin within the institutional normal limits
- •White blood cell (WBC) count between 2,500-12,000/mm^3
- •WBC differential absolute cell counts either within institutional normal range or accompanied by site Principal Investigator (PI) or Associate Investigator (AI) approval, except neutrophils and lymphocytes must specifically be within the range of greater than or equal to 0.75 x the lower limit of normal (LLN) and lees than or equal to 1.25 x the upper limit of normal (ULN) for neutrophil and lymphocyte absolute counts
- •Platelets = 125,000-500,000/m^3
- •Alanine aminotransferase (ALT) less than or equal to 1.25 x ULN based on the institutional normal range
- •Serum creatinine less than or equal to 1.1 x ULN based on the institutional normal range
- •Negative for HIV infection by an FDA approved method of detection
- •Woman-specific (if presumed to be of childbearing potential):
- •Agrees to use effective means of birth control from at least 21 days prior to enrollment through the end of the study.
- •Negative beta-HCG (human chorionic gonadotropin) pregnancy test (urine or serum) on day of enrollment.
排除标准
- •A participant was excluded if one or more of the following conditions apply:
- •Woman-specific:
- •Breast-feeding or planning to become pregnant through the end of study.
- •Participant has received any of the following:
- •An investigational HIV vaccine.
- •Systemic glucocorticoid use equal or greater than prednisone 20mg/day within 4 weeks prior to enrollment, or other medication use likely to impair vaccine response.
- •Blood products within 16 weeks prior to enrollment.
- •Live attenuated vaccines within 4 weeks prior to enrollment.
- •Inactivated vaccines within 2 weeks prior to enrollment.
- •Investigational research agents within 4 weeks prior to enrollment.
- •Current allergen immunotherapy with antigen injections, unless on maintenance schedule.
- •Current anti-tuberculosis (TB) prophylaxis or therapy.
- •Participant had any of the following:
- •Serious reactions to vaccines that preclude receipt of study injections as determined by the principal investigator or designee.
- •Hereditary angioedema, acquired angioedema, or idiopathic forms of angioedema.
- •Hypertension that is not well controlled.
- •Evidence of significant autoimmune disease or immunodeficiency.
- •Idiopathic urticaria within the past year.
- •Bleeding disorder diagnosed by a doctor (e.g. factor deficiency, coagulopathy, or platelet disorder requiring special precautions) or significant bruising or bleeding difficulties with IM injections or blood draws.
- •Seizure disorder other than: 1) febrile seizures, 2) seizures secondary to alcohol withdrawal more than 3 years ago, or 3) seizures that have not required treatment within the last 3 years.
- •Asplenia or functional asplenia.
- •Any other chronic or clinically significant condition that in the opinion of the investigator would jeopardize the safety or rights of the study subject including but not limited to: diabetes mellitus type I, chronic hepatitis; OR clinically significant forms of: drug or alcohol abuse, asthma, psychiatric disorders, heart disease, or cancer.
研究组 & 干预措施
Group 1: Trimer 4571 (100 mcg) IM with alum
Trimer 4571 injections (100 mcg), with 500 mcg of alum field mixed, administered intramuscularly (IM) in a 1 mL volume by Needle/Syringe on Day 0, Week 8, and Week 20
干预措施: Alum Adjuvant (Other)
Group 4: Trimer 4571 (500 mcg) SC with alum
Trimer 4571 injections (500 mcg), with 500 mcg of alum field mixed, administered subcutaneously (SC) in a 1 mL volume by Needle/Syringe on Day 0, Week 8, and Week 20
干预措施: Alum Adjuvant (Other)
Group 2: Trimer 4571 (100 mcg) SC with alum
Trimer 4571 injections (100 mcg), with 500 mcg of alum field mixed, administered subcutaneously (SC) in a 1 mL volume by Needle/Syringe on Day 0, Week 8, and Week 20
干预措施: Alum Adjuvant (Other)
Group 3: Trimer 4571 (500 mcg) IM with alum
Trimer 4571 injections (500 mcg), with 500 mcg of alum field mixed, administered intramuscularly (IM) in a 1 mL volume by Needle/Syringe on Day 0, Week 8, and Week 20
干预措施: Alum Adjuvant (Other)
Group 4: Trimer 4571 (500 mcg) SC with alum
Trimer 4571 injections (500 mcg), with 500 mcg of alum field mixed, administered subcutaneously (SC) in a 1 mL volume by Needle/Syringe on Day 0, Week 8, and Week 20
干预措施: VRC-HIVRGP096-00-VP (Biological)
Group 3: Trimer 4571 (500 mcg) IM with alum
Trimer 4571 injections (500 mcg), with 500 mcg of alum field mixed, administered intramuscularly (IM) in a 1 mL volume by Needle/Syringe on Day 0, Week 8, and Week 20
干预措施: VRC-HIVRGP096-00-VP (Biological)
Group 2: Trimer 4571 (100 mcg) SC with alum
Trimer 4571 injections (100 mcg), with 500 mcg of alum field mixed, administered subcutaneously (SC) in a 1 mL volume by Needle/Syringe on Day 0, Week 8, and Week 20
干预措施: VRC-HIVRGP096-00-VP (Biological)
Group 1: Trimer 4571 (100 mcg) IM with alum
Trimer 4571 injections (100 mcg), with 500 mcg of alum field mixed, administered intramuscularly (IM) in a 1 mL volume by Needle/Syringe on Day 0, Week 8, and Week 20
干预措施: VRC-HIVRGP096-00-VP (Biological)
结局指标
主要结局
Number of Participants Reporting Local Reactogenicity Signs and Symptoms For 7 Days After Each Product Administration
时间窗: 7 days after study product administration, at approximately Week 1, Week 9 and Week 21
Participants recorded the occurrence of solicited symptoms on a diary card for 7 days after each study product administration and reviewed the diary card with clinic staff at a follow up visit. Participants were counted once for each symptom at the worst severity if they indicated experiencing the symptom more than one time at any severity during the reporting period. The number reported for "Any Local Symptom" is the number of participants reporting any local symptom at the worst severity. Reactogenicity grading (Mild, Moderate, Severe) was done using the U.S. Department of Health and Human Services, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Division of AIDS (DAIDS) Table for Grading the Severity of Adult and Pediatric Adverse Events, Corrected Version 2.1.
Number of Participants Reporting Systemic Reactogenicity Signs and Symptoms for 7 Days After Each Product Administration
时间窗: 7 days after study product administration, at approximately Week 1, Week 9 and Week 21
Participants recorded the occurrence of solicited symptoms on a diary card for 7 days after the study product administration and reviewed the diary card with clinic staff at a follow up visit. Participants were counted once for each symptom at the worst severity if they indicated experiencing the symptom more than one time at any severity during the reporting period. The number reported for "Any Systemic Symptom" is the number of participants reporting any systemic symptom at the worst severity. Reactogenicity grading (Mild, Moderate, Severe) was done using the U.S. Department of Health and Human Services, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Division of AIDS (DAIDS) Table for Grading the Severity of Adult and Pediatric Adverse Events, Corrected Version 2.1.
Number of Participants With Abnormal Laboratory Measures of Safety
时间窗: Through 40 weeks after the first study product administration
Any abnormal laboratory results recorded as unsolicited adverse events (AEs) are summarized. Labs included hematology (hemoglobin, hematocrit, mean corpuscular volume (MCV), platelets, white blood cell (WBC), red blood cell (RBC), neutrophil, lymphocyte, monocyte, eosinophil and basophil counts) and chemistry (alanine aminotransferase (ALT) and creatinine). Complete blood count (CBC) with differential, creatine and ALT results were collected at screening, Day 0 prior to the first study product administration (baseline), and Weeks 1-2 after the 1st administration, Week 8 (2nd product administration), and Weeks 9-10 after the 2nd administration, Week 20 (3rd product administration), and Weeks 21-22 after the 3rd administration. Institutional laboratory normal ranges as well as the DAIDS Table for Grading the Severity of Adult and Pediatric Adverse Events, Corrected Version 2.1 were used.
Number of Participants With One or More Unsolicited Non-Serious Adverse Events (AEs)
时间窗: Through 28 days after each study product administration, up to Week 24
Unsolicited AEs and attribution assessments were recorded in the study database from receipt of each study product administration through the visit scheduled at 28 days (or 4 weeks) after each study product administration. At other time periods greater than the 28-day (or 4-week) post product administration visit, only serious AEs (SAEs reported as a separate outcome and in the AE module), and new chronic medical conditions that required ongoing medical management were recorded through the last study visit. The relationship between an AE and the study product was assessed by the investigator based on clinical judgment and the definitions outlined in the protocol. A participant with multiple experiences of the same event is counted once using the event of worst severity. If a participant had several AEs and some were evaluated as related and some as unrelated to study product, the participant is counted once as having the related event.
Number of Participants With Serious Adverse Events (SAEs)
时间窗: Through 40 weeks after the first study product administration
SAEs were recorded from receipt of the study product administration through the last expected study visit at Week 40. The relationship between a SAE and the study product was assessed by the investigator based on clinical judgment and the definitions outlined in the protocol. A participant with multiple experiences of the same event is counted once using the event of worst severity.
次要结局
- Antibody Response to Adjuvanted Trimer 4571 at 2 Weeks After the Final Study Product Administration(Baseline through Study Week 22, at 14 days after the final study product administration.)