Combinatorial Therapy With a Therapeutic Conserved Element DNA Vaccine, MVA Vaccine Boost, TLR9 Agonist and Broadly Neutralizing Antibodies: a Proof-of-concept Study Aimed at Inducing an HIV Remission
概览
- 阶段
- 1 期
- 干预措施
- Combination Intervention
- 疾病 / 适应症
- HIV/AIDS
- 发起方
- University of California, San Francisco
- 入组人数
- 11
- 试验地点
- 1
- 主要终点
- Grade 3 or Greater Adverse Event Count
- 状态
- 进行中（未招募）
- 最后更新
- 2个月前
概览
简要总结
Combination approaches will almost certainly be required to generate durable control of HIV in the absence of antiretroviral therapy (a "remission"). In this study, 20 individuals will receive a combination regimen administered during ART and then undergo an analytic treatment interruption (ATI).
详细描述
The investigators will perform a single arm study of twenty individuals with HIV infection on effective ART. All participants will receive a combination regimen administered during ART and then undergo an analytic treatment interruption. Our strategy has five stages 1. IL-12 adjuvanted p24CE DNA prime (p24CE/IL-12) at Weeks 0 and 4 2. IL-12 adjuvanted DNA boost (p24CE plus p55gag) at Week 12 3. MVA/HIV62B (MVA62B) boost at Week 20 4. single dose of two bNAbs (VRC07-523LS and 10-1074, which target CD4 binding site and V3 loop, respectively) at week 24 with a TLR9 agonist (lefitolimod) administered weekly between Weeks 24 and 33 (10 doses) 5. ATI with single dose of VRC07 and 10-1074 at Week 34 Follow-up off ART will occur through at least Week 46 (expected) and on or off ART (depending on outcome) through Week 86. Should this approach work, viral load would be expected to rebound in all individuals a few weeks after the bNAb levels decrease to sub-therapeutic levels. This acute rebound would be followed by a new lower viral load set-point and perhaps a long-term remission.
研究者
Steven Deeks
Professor in Residence
University of California, San Francisco
入排标准
入选标准
- •Willing and able to provide written informed consent.
- •Age ≤67 years at the time of enrollment for those who started treatment during early infection and \<65 years for those who started treatment during chronic infection.
- •Documented HIV-1 infection.
- •On continuous antiretroviral therapy for at least 12 months without any interruptions of greater than 14 consecutive days within the last 1 year, and on a stable regimen that does not include an non-nucleoside reverse transcriptase inhibitor (NNRTI) for at least 4 weeks, without plans to modify ART during the study period.
- •Screening plasma HIV RNA levels below the level of quantification on all available determinations in past 24 months.
- •Screening CD4+ T-cell count ≥ 500 cells/mm
排除标准
- •Subjects receiving a non-nucleoside reverse transcriptase inhibitor
- •Pregnant, breastfeeding, or unwilling to practice birth control during participation in the study
- •High-level resistance to both 10-1074 and VRC-07 as defined using the PhenoSense Neutralizing Antibody Assay (Monogram Biosciences).
- •Any history of an HIV-associated malignancy, including Kaposi's sarcoma and any type of lymphoma, or virus-associated cancers.
- •Active or recent non-HIV-associated malignancy requiring systemic chemotherapy or surgery in the preceding 36 months or for whom such therapies are expected in the subsequent 12 months.
- •CD4+ T cell nadir \<350 cells/mm3 during the chronic phase of infection (beginning 6 months following the estimated infection date and confirmed on repeat testing).
- •Active hepatitis B (HBV) infection defined as positive HBV surface antigen test.
- •9\. Active hepatitis C (HCV) infection.
- •Presence of significant abnormalities on electrocardiogram.
- •History of potential immune-mediated medical conditions. Individuals with isolated Raynaud's phenomenon or localized disease requiring topical therapy alone will not be excluded.
研究组 & 干预措施
Combination intervention arm
All volunteers will receive the combination intervention outlined above.
干预措施: Combination Intervention
结局指标
主要结局
Grade 3 or Greater Adverse Event Count
时间窗: Week 0 through 102
Number of participants who experience a new grade 3 or greater adverse event
Proportion of Participants Achieving Post-treatment Control
时间窗: Week 34 through 86
This will be defined as: 1. Participants who fail to show any consistent rebound above 400 copies RNA/mL between Week 12 of the ATI (when bNAb levels wane) and Week 36 of the ATI 2. Participants who exhibit a rebound and eventually achieve 24 weeks of virus control will be considered as having achieved post-treatment control
次要结局
- Any Grade 2, 3 or 4 Adverse Event Through Week 62(Week 0 through 62)
- Any Serious Adverse Events, Medically Attended Adverse Event, and Potentially Immune-mediated Medical Condition(Week 0 through 86)
- Magnitude of T Cell Responses(Week 22)
- Breadth of T Cell Responses(Week 22)
- Intact Provirus DNA Levels(Baseline to pre-interruption (week 34))