Phase 1 Study of Multikine in the Treatment of Perianal Warts
试验速览
- 阶段
- 1 期
- 状态
- 终止
- 发起方
- 入组人数
- 4
- 试验地点
- 1
- 主要终点
- Wart characterization change is being assessed
研究概览
简要总结
Caused by the human papillomavirus (HPV), anogenital warts are a common sexually-transmitted infection (STI). They are distressing to those who have them and are a source of viral shedding and transmission to others. Treatment of warts is aimed at destruction of the lesion.
Objectives:
- Establish safety of Multikine in treatment of perianal condyloma.
- Describe presence of anal HPV and anal dysplasia in participants with perianal condyloma.
- Describe adverse effects associated with Multikine in the management of perianal condyloma.
Design:
Phase I, dose-escalation trial. Potential participants desiring treatment for their perianal warts will be referred to study by their primary clinician. All participants will undergo baseline anal Pap, anal HPV subtyping, perianal condyloma characterization (count, measurement, photography), and complete a baseline questionnaire. Cohort A participants will undergo perilesional Multikine injections (200IU) once daily, Monday through Friday, for 14 days, off for 14 days, then again once daily, Monday through Friday for 14 days. If no serious adverse events are noted after 4 weeks of therapy, cohort B will be studied using the same schedule but with a dose of 400IU per treatment. Each participant will undergo anal Pap and anal HPV subtyping once weekly during treatment. Condyloma characterization (count, measurement, photography) will occur prior to each treatment. After treatment completed, participants will complete a follow-up visit at 70, 100, 130, 160 days and have anal Pap, anal HPV subtyping, and perianal condyloma characterization (count, measurement, photography) performed.
Subjects:
The study will be open to adult men and women who are HIV-infected who receive medical care from the Naval Medical Center San Diego.
Main Outcome Measures:
- Perianal wart characterization [count, measurement (in millimeters diameter)], photography)
- HPV subtype in anal canal
- Anal dysplasia cytologic grade
- Questionnaire responses
- Adverse effects experienced during treatment, recorded in symptom log
详细描述
There are no further details to describe regarding this research project
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •≥18 years of age
- •Diagnosed with perianal condyloma by primary clinician
- •HIV-infected, may be on or off of antiretroviral therapy
- •any CD4 count will be considered appropriate for study
- •Blood WBC > 2.0x103/mm3 and absolute neutrophils count > 500
- •Blood hemoglobin > 10.0 g/dL
- •Blood platelet count > 50x103/mm3
- •Serum total bilirubin < 6.0 mg/dL (participants taking atazanavir-based ARV regimens may have elevated total bilirubin but are generally < 6)
- •Blood aspartate aminotransferase (AST) < 100 U/L (<2 ULN)
- •Blood alanine aminotransferase (ALT) < 130 U/L (<2 ULN)
- •Serum creatinine < 1.5 mg/dL
- •ECOG performance status < 3
- •If a subject is of reproductive potential he/she and her/his sexual partner MUST be willing and able to utilize effective methods of contraception (e.g., birth control pill, barrier methods with spermicide - as applicable) for the duration of the study including the study follow-up period.
排除标准
- •Anal cancer (current or history of)
- •Inability to attend study visits
- •Participation in any other drug study
- •History of asthma
- •History of organ transplantation or requiring chronic administration of immune suppressive drugs in the last 6 months
- •For women, neither pregnant nor lactating
- •In the opinion of the PI, the subject may not be able to tolerate the study treatment regimen
研究组 & 干预措施
Cohort A
Cohort A participants will undergo perilesional Multikine injections (200IU) once daily, Monday through Friday, for 14 days, off for 14 days, then again once daily, Monday through Friday for 14 days.
干预措施: Leukocyte Interleukin, Injection 200IU (Drug)
Cohort B
Cohort B participants will undergo perilesional Multikine injections 400IU once daily, Monday through Friday, for 14 days, off for 14 days, then again once daily, Monday through Friday for 14 days.
干预措施: Leukocyte Interleukin, injection 400IU (Drug)
结局指标
主要结局
Wart characterization change is being assessed
时间窗: Days 0, 4, 11, 32, 39, 70, 100, 130, 160
Perianal wart characterization includes counting the number of identified warts, the diameter measurement of each identified wart in millimeters and the photographic imaging of each identified wart during the treatment phase and the follow-up phase of the study
次要结局
- HPV subtype identification change is being assessed(Days 0, 4, 11, 32, 39, 70, 100, 130, 160)
- Anal dysplasia cytologic grade change is being assessed(Days 0, 4, 11, 32, 39, 70, 100, 130, 160)
- Adverse effects during the treatment phase of the study are being assessed(Days 0, 4, 11, 32, 39, 70, 100, 130, 160)