- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07743593
Optimizing Care for Cryptococcal Antigenemia: Evaluation of Short Course Fluconazole and ART Timing Among CrAg+ Persons With Low Titers
This randomized clinical trial will evaluate the optimal duration of fluconazole therapy and timing of antiretroviral therapy initiation among HIV-infected persons with asymptomatic cryptococcal antigenemia and low cryptococcal antigen titers in Uganda.
Participants with low-titer cryptococcal antigenemia will be followed to assess whether a shorter 10-week course of fluconazole is non-inferior to the standard 24-week fluconazole regimen for 24-week cryptococcal meningitis-free survival. Among participants eligible for antiretroviral therapy timing randomization, the study will also compare immediate antiretroviral therapy initiation with delayed initiation after 14 days to evaluate 10-week hospitalization-free survival.
Participants will be followed for up to 24 weeks, with study visits and contacts to assess survival, cryptococcal meningitis, hospitalizations, adverse events, and fluconazole adherence.
Studieoversikt
Status
Detaljert beskrivelse
Cryptococcal antigenemia can be detected in the blood before the development of symptomatic cryptococcal meningitis and is associated with increased risk of meningitis and death among persons with advanced HIV disease. Current guidelines recommend cryptococcal antigen screening and preemptive fluconazole therapy for persons with asymptomatic cryptococcal antigenemia, but the optimal duration of fluconazole therapy and the optimal timing of antiretroviral therapy initiation remain uncertain.
This randomized clinical trial will enroll HIV-infected persons with asymptomatic cryptococcal antigenemia and low cryptococcal antigen titers in Uganda. The study is designed to answer two main questions. First, it will evaluate whether a shorter 10-week course of fluconazole is non-inferior to the standard 24-week fluconazole regimen for 24-week cryptococcal meningitis-free survival. Second, among participants eligible for antiretroviral therapy timing randomization, it will evaluate whether immediate antiretroviral therapy initiation is non-inferior to delayed initiation after 14 days for 10-week hospitalization-free survival.
At enrollment, eligible participants who meet criteria for antiretroviral therapy timing randomization will be randomized to immediate antiretroviral therapy initiation or delayed antiretroviral therapy initiation after 14 days. All participants will receive fluconazole 800 mg daily beginning at enrollment and continuing for 14 days, followed by fluconazole 400 mg daily through week 10. At week 10, participants who are alive and have not developed cryptococcal meningitis will be randomized to stop fluconazole or to continue fluconazole 200 mg daily for an additional 14 weeks, for a total fluconazole duration of 24 weeks.
Participants will be followed at weeks 2, 4, 6, 8, 10, 16, 20, and 24. Study assessments will include interval history, vital status, assessment for signs and symptoms of cryptococcal meningitis, medication review and adherence assessment, physical examination or symptom-directed examination as appropriate, and adverse event monitoring. Participants who miss visits or cannot attend scheduled clinic visits may be contacted by phone or through home visits to assess vital status and meningitis events.
The primary fluconazole-duration endpoint is 24-week cryptococcal meningitis-free survival with retention in care. The primary antiretroviral therapy timing endpoint is 10-week hospitalization-free survival with retention in care. Secondary endpoints include survival, incidence of cryptococcal meningitis, grade 3 to 5 clinical adverse events or serious adverse events, hospitalization, death, and fluconazole adherence.
Studietype
Registrering (Antatt)
Fase
- Fase 3
Kontakter og plasseringer
Studiekontakt
- Navn: Radha Rajasingham, MD
- Telefonnummer: 612-625-4680
- E-post: radha@umn.edu
Studiesteder
-
-
-
Kampala, Uganda
- Infectious Diseases Institute, Makerere University
-
Ta kontakt med:
- Radha Rajasingham, MD
- Telefonnummer: 612-625-4680
- E-post: radha@umn.edu
-
Hovedetterforsker:
- Radha Rajasingham, MD
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- HIV-1 infection
- Age greater than 18 years
- Ability and willingness to give informed consent
- Plasma or serum cryptococcal antigen positive with titer less than 1:160
Exclusion Criteria:
- Cannot or unlikely to attend regular clinic visits
- History of cryptococcal infection
- Symptomatic meningitis confirmed by cerebrospinal fluid cryptococcal antigen positivity
- More than 10 weeks of fluconazole therapy
- Pregnancy confirmed by urinary or serum pregnancy test
- Current breastfeeding
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Sekvensiell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Immediate ART + 10-Week Fluconazole Arm Type:
Participants eligible for ART timing randomization will initiate antiretroviral therapy immediately at enrollment.
Participants who are alive and have not developed cryptococcal meningitis at week 10 will stop fluconazole after completing 10 weeks of preemptive fluconazole therapy.
|
Antiretroviral therapy will be initiated immediately at enrollment for participants randomized to immediate ART initiation.
ART drug choice will be per clinical standard of care.
Participants will receive fluconazole 800 mg daily for 14 days, followed by fluconazole 400 mg daily through week 10, then stop fluconazole.
|
|
Eksperimentell: Immediate ART + 24-Week Fluconazole
Participants eligible for ART timing randomization will initiate antiretroviral therapy immediately at enrollment.
Participants who are alive and have not developed cryptococcal meningitis at week 10 will continue fluconazole through 24 weeks of preemptive fluconazole therapy.
|
Antiretroviral therapy will be initiated immediately at enrollment for participants randomized to immediate ART initiation.
ART drug choice will be per clinical standard of care.
Participants will receive fluconazole 800 mg daily for 14 days, followed by fluconazole 400 mg daily through week 10, then fluconazole 200 mg daily for an additional 14 weeks, for a total fluconazole duration of 24 weeks.
|
|
Eksperimentell: Delayed ART + 10-Week Fluconazole
Participants eligible for ART timing randomization will delay antiretroviral therapy initiation until 14 days after enrollment.
Participants who are alive and have not developed cryptococcal meningitis at week 10 will stop fluconazole after completing 10 weeks of preemptive fluconazole therapy.
|
Participants will receive fluconazole 800 mg daily for 14 days, followed by fluconazole 400 mg daily through week 10, then stop fluconazole.
Antiretroviral therapy will be initiated 14 days after enrollment for participants randomized to delayed ART initiation.
ART drug choice will be per clinical standard of care.
|
|
Aktiv komparator: Delayed ART + 24-Week Fluconazole
Participants eligible for ART timing randomization will delay antiretroviral therapy initiation until 14 days after enrollment.
Participants who are alive and have not developed cryptococcal meningitis at week 10 will continue fluconazole through 24 weeks of preemptive fluconazole therapy.
|
Participants will receive fluconazole 800 mg daily for 14 days, followed by fluconazole 400 mg daily through week 10, then fluconazole 200 mg daily for an additional 14 weeks, for a total fluconazole duration of 24 weeks.
Antiretroviral therapy will be initiated 14 days after enrollment for participants randomized to delayed ART initiation.
ART drug choice will be per clinical standard of care.
|
|
Eksperimentell: ART-Experienced + 10-Week Fluconazole
Participants who are already receiving ART or are not eligible for ART timing randomization will continue ART per standard clinical care.
Participants who are alive and have not developed cryptococcal meningitis at week 10 will stop fluconazole after completing 10 weeks of preemptive fluconazole therapy.
|
Participants will receive fluconazole 800 mg daily for 14 days, followed by fluconazole 400 mg daily through week 10, then stop fluconazole.
|
|
Aktiv komparator: ART-Experienced + 24-Week Fluconazole
Participants who are already receiving ART or are not eligible for ART timing randomization will continue ART per standard clinical care.
Participants who are alive and have not developed cryptococcal meningitis at week 10 will continue fluconazole through 24 weeks of preemptive fluconazole therapy.
|
Participants will receive fluconazole 800 mg daily for 14 days, followed by fluconazole 400 mg daily through week 10, then fluconazole 200 mg daily for an additional 14 weeks, for a total fluconazole duration of 24 weeks.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
24-week cryptococcal meningitis-free survival with retention in care
Tidsramme: 24 weeks
|
Cryptococcal meningitis-free survival with retention in care at 24 weeks will be compared between participants randomized to 10 weeks of fluconazole and participants randomized to 24 weeks of fluconazole.
Participants who develop cryptococcal meningitis, die, or are not retained in care will be considered treatment failures.
|
24 weeks
|
|
10-week hospitalization-free survival with retention in care
Tidsramme: 10 weeks
|
Hospitalization-free survival with retention in care at 10 weeks will be compared between participants randomized to immediate antiretroviral therapy initiation and participants randomized to delayed antiretroviral therapy initiation.
Hospitalization-free survival will include assessment of events such as meningitis, serious opportunistic infections, immune reconstitution inflammatory syndrome events, hospitalization, death, and retention in care.
|
10 weeks
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Incidence of grade 3 to 5 clinical adverse events or serious adverse events
Tidsramme: Up to 24 weeks
|
Incidence of grade 3 to 5 clinical adverse events or serious adverse events will be assessed among enrolled participants.
|
Up to 24 weeks
|
|
24-week known survival
Tidsramme: 24 weeks
|
Known survival at 24 weeks will be assessed.
Death and loss to follow-up will be considered therapeutic failures.
|
24 weeks
|
|
Incidence of cryptococcal meningitis
Tidsramme: Up to 24 weeks
|
Incidence of cryptococcal meningitis will be assessed during study follow-up.
|
Up to 24 weeks
|
|
Incidence of hospitalization
Tidsramme: Up to 24 weeks
|
Incidence of hospitalization, irrespective of cause, will be assessed during study follow-up.
|
Up to 24 weeks
|
|
Incidence of death
Tidsramme: Up to 24 weeks
|
Incidence of death, irrespective of cause, will be assessed during study follow-up.
|
Up to 24 weeks
|
|
Fluconazole adherence
Tidsramme: Up to 24 weeks
|
Fluconazole adherence will be assessed using self-reported compliance, pharmacy records, and tablet counts when available.
|
Up to 24 weeks
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Radha Rajasingham, MD, University of Minnesota
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- Nevroinflammatoriske sykdommer
- Sykdommer i sentralnervesystemet
- Sykdommer i nervesystemet
- Infeksjoner
- Bakterielle infeksjoner og mykoser
- Infeksjoner i sentralnervesystemet
- Meningitt, sopp
- Soppinfeksjoner i sentralnervesystemet
- Mykoser
- Kryptokokkose
- Meningitt
- Meningitt, kryptokok
- Heterocykliske forbindelser, 1-ring
- Heterocykliske forbindelser
- Azoler
- Triazoler
- Flukonazol
Andre studie-ID-numre
- STUDY00024821
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
produkt produsert i og eksportert fra USA
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .