CTRI/2013/04/003545招募中1 期
A Phase I/II Dose-Finding Study of High-Dose Fluconazole Treatment in AIDS-Associated Cryptococcal Meningitis
Division of AIDS DAIDS NIH USA Division of AIDS DAIDS NIH USA0 个研究点目标入组 192 人开始时间: 待定最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 192
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Inclusion Criteria - Step 1
- •?Cryptococcal meningitis documented either by a positive CSF cryptococcal culture, a positive CSF India ink preparation, or a positive CSF cryptococcal antigen latex agglutination test within 7 days prior to entry
- •?CSF collection for quantitative cryptococcal culture within 72 hours prior to study entry or planned to be performed at study entry
- •?HIV-1 infection documented by any licensed rapid HIV test or HIV enzyme or chemiluminescence immunoassay (E/CIA) test kit at any time prior to study entry and confirmed by a licensed Western blot or a second antibody test by a method other than the initial rapid HIV and/or E/CIA, or by HIV-1 antigen, plasma HIV-1 RNA viral load
- •?Ability to take oral medications.
- •?For patients with a co-morbid complication of HIV, including opportunistic infections, receipt of stable treatment for the co-morbid complication and clinically stable, as judged by the site investigator
- •?For female participants of reproductive potential a negative serum or urine pregnancy test result must be obtained within 3 days prior to study entry
- •?All participants must agree not to participate in the conception process (e.g., active attempt to become pregnant or to impregnate, sperm donation, in vitro fertilization).
- •?If participating in sexual activity that could lead to pregnancy, participants must use a form of contraceptive listed below while on study treatment and for 6 weeks after has been discontinued
- •?Willingness and ability to adhere to dose schedules and mandatory procedures
- •?Measured or calculated creatinine clearance of 50 mL/min or more within 3 days prior to study entry
- •?Required laboratory values within 3 days prior to study entry. More information on this criterion can be found in the study protocol
- •?Ability and willingness of the participant or legal guardian/representative to give informed consent
- •?Availability at the site of at least 2 weeks of its standard of care ampho B-based regimen
- •Inclusion Criterion - Step 2
- •?Randomization to an ampho B-based regimen in Step 1
- •?Receipt of at least one dose of ampho B-based regimen in Step 1
- •?Premature discontinuation of ampho B in response to the occurrence of any treatment-limiting toxicity, as described in section 5 of the A5225/HiFLAC MOPS
- •Inclusion Criteria - Step 3
- •?For participants in Step 1 who are currently receiving study-provided fluconazole, a negative CSF culture after 2 weeks incubation from a sample obtained at or before week 6 (day 35-49)
- •?For participants in Step 1 who are currently receiving an ampho B-based regimen or alternative treatment, completion of approximately 2 weeks of treatment
- •?For participants in Step 2 who are currently receiving study-provided fluconazole, negative CSF culture after 2 weeks incubation from a sample obtained at or before week 6 (day 35-49).
- •Inclusion Criteria - Step 4
- •?On study treatment at week 10 (day 63-77)
排除标准
- •Exclusion Criteria - Step 1
- •?Expected survival of 2 weeks or less, in the opinion of the site investigator
- •?For patients with a co-morbid complication of HIV, anticipated difficulty, in the opinion of the site investigator, in judging response to study treatment as a result of the co-morbid complication or the drugs used to treat it
- •?A prior episode of CM, either as indicated by patient or as noted in patient medical records
- •?Use of certain drugs, within specified time periods. More information on this criterion can be found in the study protocol.
- •?Suspected or active tuberculosis (TB), even if untreated, for participants screening at the time that a 1200 mg daily fluconazole induction cohort is enrolling
- •?Known allergy, sensitivity to, or intolerance of fluconazole or other imidazole or triazole compounds, or to ampho B or other components of the standard of care ampho-B based regimen
- •?History of clinically significant cardiac disease, in opinion of site investigator, including symptoms of ischemia, coronary artery disease, congestive heart failure, or arrhythmia
- •?ECG (electrocardiogram) with QTc interval greater than 450 msec within 7 days prior to study entry.
- •?History of CNS disorder (excluding mood disorders) or concurrent CNS disorder(s) that, in the opinion of the investigator, would interfere with assessment of efficacy (e.g., ability to perform CSF sampling) such as lymphoma, neurocysticercosis, or toxoplasmosis
- •?Receipt of investigational drug therapy within 30 days prior to study entry without prior approval
- •?Receipt of specified treatments for the current episode of CM. More information on this criterion can be found in the study protocol.
- •?Active drug or alcohol use, dependence, or other conditions that in the opinion of the site investigator would jeopardize the safety of a participant in the study or would render the person unable to comply with the study plan
- •?Breast-feeding
- •Exclusion Criterion - Step 2
- •?Receipt of fluconazole monotherapy in Step 1
- •?Receipt of 8.4 mg/kg or more of ampho B
- •?At or beyond Day 17 in Step 1.
- •Exclusion Criteria - Step 3
- •?On study treatment beyond week 10 (day 77) in Step 1 or Step 2
- •Exclusion Criteria - Step 4
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