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临床试验/NCT06666322
NCT06666322招募中2 期

Platform Trial For Cryptococcal Meningitis

David Boulware2 个研究点 分布在 1 个国家目标入组 2,000 人开始时间: 2025年5月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
2,000
试验地点
2
主要终点
Rate of cerebrospinal fluid (CSF) Cryptococcus clearance (Early Fungicidal Activity, or EFA)

研究概览

简要总结

Cryptococcal meningitis is a fungal infection that causes a severe syndrome of meningitis that is 100% fatal without antifungal therapy. Even with antifungal therapy, mortality rates remain high, especially in low and middle income countries where the ongoing HIV/AIDS pandemic increases the risk of cryptococcosis among persons living with HIV infection. The combination of amphotericin and flucytosine (5-FC) has been the mainstay of therapy for the initial management of cryptococcal meningitis for 4 decades. Indeed, the effective delivery of these first line therapy in Africa can lower mortality to 25%. However, several challenges exist. First, even while 5-FC is included on the WHO list of essential medicines, the availability of 5-FC worldwide is limited. Second, liposomal amphotericin (Ambisome ®) is currently available from a single source supplier, creating risk. Third, current therapies have substantial toxicity. Lastly, with widespread agricultural fungicide use of azoles, the median fluconazole minimum inhibitory concentration (MIC50 ) for Cryptococcus has doubled since 2013. Globally, new or improved antifungals are needed for cryptococcal meningitis, particularly those which have less toxicity, greater efficacy, a prolonged half-life, and minimal drug-drug interactions.

As multiple new antifungal medicines are on the horizon, this platform trial utilizes a master protocol to investigate, multiple antifungal regimens using standardized eligibility criteria, standardized study schedule of events, and standardized contemporary endpoints.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • CSF cryptococcal antigen (CrAg) positive meningitis
  • Living with HIV
  • Ability and willingness to provide informed consent
  • Willing to receive protocol-specified lumbar punctures
  • Age >= 18 years
  • Female participants of childbearing potential who are participating in sexual activity that could lead to pregnancy must agree to use reliable forms of contraception (duration will be indicated in each Trial Appendix).

排除标准

  • Received 3 or more doses of antifungal therapy for meningitis within last 30 days
  • Inability to take enteral (oral or nasogastric) medicine
  • Cannot or unlikely to attend regular clinic visits
  • Receiving chemotherapy or corticosteroids
  • Receiving hemodialysis or known liver cirrhosis
  • Suspected Paradoxical immune reconstitution inflammatory syndrome (IRIS)
  • Pregnancy or breastfeeding
  • Previous administration of investigational study drug
  • Any condition for which participation would not be in the best interest of the participant or that could limit protocol specified assessments
  • Trial Appendix study-drug specific eligibility criteria

研究组 & 干预措施

Control group

Active Comparator

randomized to standard of care

干预措施: Standard of care (Drug)

Experimental group 1

Experimental

randomized to experimental antifungal therapy #1

干预措施: Oteseconazole - antifungal therapy 1 (Drug)

Experimental group 2

Experimental

randomized to experimental antifungal therapy #2

干预措施: Turletricin injection - antifungal therapy 2 (Drug)

Experimental group 4

Experimental

randomized to experimental antifungal therapy #4

干预措施: Oteseconazole with Flucytosine - antifungal therapy 4 (Drug)

Experimental group 3

Experimental

randomized to experimental antifungal therapy #3

干预措施: Turletricin Injection - antifungal therapy 3 (Drug)

结局指标

主要结局

Rate of cerebrospinal fluid (CSF) Cryptococcus clearance (Early Fungicidal Activity, or EFA)

时间窗: 2 weeks

quantified by the change of log 10 Cryptococcus CFU/mL CSF/day as measured by serial quantitative CSF fungal cultures over \~2 weeks.

All-cause mortality

时间窗: 2 weeks

measured at 2-weeks

次要结局

  • Desirability of Outcome Response (DOOR) as ordinal ranked maximum score tested by Win Ratio.(18 weeks)
  • Survival time through 18 weeks without Cryptococcus culture-positive relapse of meningitis(18 weeks)
  • CSF culture sterility (cumulative incidence over 18 weeks)(18 weeks)
  • 18-week survival time(18 weeks)
  • Use of rescue/additional IV amphotericin beyond scheduled use(18 weeks)
  • Modified Rankin score on functional status at 18 weeks(18 weeks)
  • Incidence of laboratory abnormalities by Grade 1-5(10 weeks)
  • Incidence of serious adverse events(18 weeks)
  • Incidence of study drug discontinuation or interruption >1 day due to toxicity, by adverse event grade.(10 weeks)

研究者

申办方类型
Other
责任方
Sponsor Investigator
主要研究者

David Boulware

McKnight Distinguished Professor of Medicine

University of Minnesota

研究点 (2)

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