RecruitingPhase 2Phase 3NCT06666322

Platform Trial For Cryptococcal Meningitis


Sponsor

University of Minnesota

Enrollment

2,000 participants

Start Date

May 28, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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 regimens using standardized eligibility criteria, standardized study schedule of events, and standardized contemporary endpoints.


Eligibility

Min Age: 18 Years

Inclusion Criteria6

  • 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).

Exclusion Criteria10

  • 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

Interventions

DRUGAntifungal therapy 3

To be determined

DRUGAntifungal therapy 4

To be determined

DRUGStandard of care

2022 WHO First Line Induction Therapy: 1. Liposomal Amphotericin B 10mg/kg IV given once 2. Flucytosine 100mg/kg/day for 14 days in divided doses 3. Fluconazole 1200mg/day for 14 days Consolidation Therapy: Fluconazole 800mg/day from 2 to 10 weeks Secondary Prophylaxis: Fluconazole 200mg/day through 1 year minimum

DRUGOteseconazole - antifungal therapy 1

Oteseconazole, is an azole metalloenzyme inhibitor targeting the fungal sterol, 14α demethylase (CYP51) * Loading doses of oral Oteseconazole 600 mg twice daily for 10 days, then 600 mg oteseconazole weekly on weeks 3, 4, 5, and 6. * Liposomal Amphotericin B 10 mg/kg IV once. * No fluconazole or 5FC to be given.

DRUGSfu-AM2-19 Injection - antifungal therapy 2

SF001 2.0 mg/kg IV administered on day 1, followed by 1.5 mg/kg on day 8 with Fluconazole 1200mg/day and flucytosine 100mg/day in divided doses x 14 days


Locations(2)

Infectious Diseases Institute

Kampala, Uganda

Mbarara University of Science and Technology

Mbarara, Uganda

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NCT06666322


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