Platform Trial For Cryptococcal Meningitis (PLATFORM-CM)

Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Minnesota

About this trial

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 criteria

Qualifiers

CSF cryptococcal antigen (CrAg) positive meningitis

Living with HIV

Ability and willingness to provide informed consent

Willing to receive protocol-specified lumbar punctures

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Standard of care
  • Oteseconazole - antifungal therapy 1
  • Turletricin injection - antifungal therapy 2
  • Turletricin Injection - antifungal therapy 3
  • Oteseconazole with Flucytosine - antifungal therapy 4

Treatment groups

2,000 Participants
are divided into 5 treatment groups

Sponsors and collaborators

University of Minnesota

Lead sponsor

Infectious Diseases Institute

Collaborator