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Adjunctive Sertraline for the Treatment of HIV-Associated Cryptococcal Meningitis (ASTRO-CM)

Primary Purpose

Cryptococcal Meningitis, Fungal Meningitis

Status
Completed
Phase
Phase 3
Locations
Uganda
Study Type
Interventional
Intervention
Sertraline
Sponsored by
University of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cryptococcal Meningitis focused on measuring cryptococcal meningitis, cryptococcus, meningitis, yeast, fungus

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Cryptococcal meningitis diagnosed by CSF cryptococcal antigen (CRAG)
  • HIV-1 infection
  • Ability and willingness of the participant or legal guardian/representative to provide informed consent
  • Willing to receive protocol-specified lumbar punctures

Exclusion Criteria:

  • Age < 18 years
  • Receipt of >=3 doses of amphotericin therapy
  • Cannot or unlikely to attend regular clinic visits
  • History of known liver cirrhosis
  • Presence of jaundice
  • Pregnancy
  • Current breastfeeding

Sites / Locations

  • Infectious Disease Institute
  • Mbarara University of Science and Technology

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Placebo

Sertraline 400mg

Arm Description

Standard cryptococcal meningitis therapy with amphotericin (0.7-1.0 mg/kg/day) + fluconazole (800-1200mg/day) + placebo

Standard cryptococcal meningitis therapy with amphotericin (0.7-1.0 mg/kg/day) + fluconazole (800-1200mg/day plus adjunctive sertraline therapy at 400mg/day for 2 weeks, then 200mg for 12 weeks, and then tapered over 3 weeks.

Outcomes

Primary Outcome Measures

Survival
18-week survival. The comparison will be between sertraline 400mg group and placebo

Secondary Outcome Measures

Safety (Occurence of Adverse Events)
Safety and tolerability of adjunctive sertraline (grade 4-5) adverse reactions
Count of Participants With Cerebrospinal Fluid Sterility
Number of participants with sterile cerebrospinal fluid at 2 weeks
Center for Epidemiologic Studies in Depression (CES-D) Scale
Center for Epidemiologic Studies in Depression (CES-D) scale at 14 weeks. CES-D scores are based on a 20 item survey with total scores ranging from 0 to 60. Higher scores suggest a greater presence of depressive symptoms. A CES-D score of 16 or higher is interpreted to indicate a risk for depression.
Quantitative Neurocognitive Performance Score (QNPZ-8)
Quantitative neurocognitive performance Z-score (QNPZ-8) at 14 weeks. The QNPZ-8 is a mean score of testing of 8 neurocognitive domains. Eqach domain is scaled based on a Z-score where the mean = 0 for the HIV-negative Ugandan population, accounting for age and educational status. Each +1 unit is one standard deviation better than the population norm. Each -1 unit is one standard deviation worse than the population norm.
Fungal Clearance as Determined by Early Fungicidal Activity of CDF
To determine whether adjunctive sertraline will lead to a faster rate of fungal clearance from cerebrospinal fluid (CSF), as measured by early fungicidal activity (EFA) of clearance of the Cryptococcus colony forming units (cfu) per mL of CSF per day, compared to standard therapy alone.
Number of Participants Experiencing IRIS OR Relapse
Cumulative incidence of central nervous system (CNS) cryptococcal-related paradoxical immune reconstitution inflammatory syndrome (IRIS) or culture-positive relapse
Event Free Survival
Event free survival of composite events of: death,central nervous system (CNS) cryptococcal-related paradoxical immune reconstitution inflammatory syndrome (IRIS) or culture-positive relapse.

Full Information

First Posted
February 27, 2013
Last Updated
June 2, 2020
Sponsor
University of Minnesota
Collaborators
Infectious Disease Institute, Kampala, Uganda, National Institute of Neurological Disorders and Stroke (NINDS), Mbarara University of Science and Technology, Medical Research Council, Wellcome Trust, Makerere University
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1. Study Identification

Unique Protocol Identification Number
NCT01802385
Brief Title
Adjunctive Sertraline for the Treatment of HIV-Associated Cryptococcal Meningitis
Acronym
ASTRO-CM
Official Title
Adjunctive Sertraline for the Treatment of HIV-Associated Cryptococcal Meningitis
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
March 9, 2015 (Actual)
Primary Completion Date
September 2017 (Actual)
Study Completion Date
September 27, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
Collaborators
Infectious Disease Institute, Kampala, Uganda, National Institute of Neurological Disorders and Stroke (NINDS), Mbarara University of Science and Technology, Medical Research Council, Wellcome Trust, Makerere University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a phase III trial to determine whether adjunctive sertraline will lead to improved survival 18-week survival. There was an initial phase I/II unmasked dose finding pharmacokinetic study of CSF concentrations in 172 persons conducted from August 2013 to August 2014. See NCT03002012.
Detailed Description
This is a phase III randomized trial to evaluate whether sertraline when added to standard amphotericin-based therapy for cryptococcal meningitis, will lead to improved survival . Cryptococcal meningitis diagnosis will be made via CSF cryptococcal antigen (CRAG) at time of lumbar puncture (LP) with confirmation by CSF culture. After informed consent, subjects that meet eligibility requirements will be able to enter study. A non-randomized phase I dose-escalation study will first be conducted to help optimize dosing for a larger randomized phase II study. Phase III Design: Subjects will be randomized to standard induction therapy with masked placebo or sertraline at 400mg/day. We will use a permutated block randomization in a 1:1 allocation (n=275 per arm). Total anticipated enrollment: 550 subjects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cryptococcal Meningitis, Fungal Meningitis
Keywords
cryptococcal meningitis, cryptococcus, meningitis, yeast, fungus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
460 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
No Intervention
Arm Description
Standard cryptococcal meningitis therapy with amphotericin (0.7-1.0 mg/kg/day) + fluconazole (800-1200mg/day) + placebo
Arm Title
Sertraline 400mg
Arm Type
Experimental
Arm Description
Standard cryptococcal meningitis therapy with amphotericin (0.7-1.0 mg/kg/day) + fluconazole (800-1200mg/day plus adjunctive sertraline therapy at 400mg/day for 2 weeks, then 200mg for 12 weeks, and then tapered over 3 weeks.
Intervention Type
Drug
Intervention Name(s)
Sertraline
Other Intervention Name(s)
Zoloft, Lustral
Intervention Description
Sertraline 400mg/day for 2 weeks, then 200mg/day for 12 weeks, then tapered over 3 weeks.
Primary Outcome Measure Information:
Title
Survival
Description
18-week survival. The comparison will be between sertraline 400mg group and placebo
Time Frame
18 weeks
Secondary Outcome Measure Information:
Title
Safety (Occurence of Adverse Events)
Description
Safety and tolerability of adjunctive sertraline (grade 4-5) adverse reactions
Time Frame
18 weeks
Title
Count of Participants With Cerebrospinal Fluid Sterility
Description
Number of participants with sterile cerebrospinal fluid at 2 weeks
Time Frame
14 days
Title
Center for Epidemiologic Studies in Depression (CES-D) Scale
Description
Center for Epidemiologic Studies in Depression (CES-D) scale at 14 weeks. CES-D scores are based on a 20 item survey with total scores ranging from 0 to 60. Higher scores suggest a greater presence of depressive symptoms. A CES-D score of 16 or higher is interpreted to indicate a risk for depression.
Time Frame
14 weeks
Title
Quantitative Neurocognitive Performance Score (QNPZ-8)
Description
Quantitative neurocognitive performance Z-score (QNPZ-8) at 14 weeks. The QNPZ-8 is a mean score of testing of 8 neurocognitive domains. Eqach domain is scaled based on a Z-score where the mean = 0 for the HIV-negative Ugandan population, accounting for age and educational status. Each +1 unit is one standard deviation better than the population norm. Each -1 unit is one standard deviation worse than the population norm.
Time Frame
14 weeks
Title
Fungal Clearance as Determined by Early Fungicidal Activity of CDF
Description
To determine whether adjunctive sertraline will lead to a faster rate of fungal clearance from cerebrospinal fluid (CSF), as measured by early fungicidal activity (EFA) of clearance of the Cryptococcus colony forming units (cfu) per mL of CSF per day, compared to standard therapy alone.
Time Frame
14 days
Title
Number of Participants Experiencing IRIS OR Relapse
Description
Cumulative incidence of central nervous system (CNS) cryptococcal-related paradoxical immune reconstitution inflammatory syndrome (IRIS) or culture-positive relapse
Time Frame
18 weeks
Title
Event Free Survival
Description
Event free survival of composite events of: death,central nervous system (CNS) cryptococcal-related paradoxical immune reconstitution inflammatory syndrome (IRIS) or culture-positive relapse.
Time Frame
18 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cryptococcal meningitis diagnosed by CSF cryptococcal antigen (CRAG) HIV-1 infection Ability and willingness of the participant or legal guardian/representative to provide informed consent Willing to receive protocol-specified lumbar punctures Exclusion Criteria: Age < 18 years Receipt of >=3 doses of amphotericin therapy Cannot or unlikely to attend regular clinic visits History of known liver cirrhosis Presence of jaundice Pregnancy Current breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David B Meya, MBCHB MMed
Organizational Affiliation
Infectious Disease Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Joshua Rhein, MD
Organizational Affiliation
University of Minnesota
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
David R Boulware, MD MPH
Organizational Affiliation
University of Minnesota
Official's Role
Study Chair
Facility Information:
Facility Name
Infectious Disease Institute
City
Kampala
Country
Uganda
Facility Name
Mbarara University of Science and Technology
City
Mbarara
Country
Uganda

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
Open
IPD Sharing Access Criteria
Contact of the Principal Investigator
Citations:
PubMed Identifier
26971081
Citation
Rhein J, Morawski BM, Hullsiek KH, Nabeta HW, Kiggundu R, Tugume L, Musubire A, Akampurira A, Smith KD, Alhadab A, Williams DA, Abassi M, Bahr NC, Velamakanni SS, Fisher J, Nielsen K, Meya DB, Boulware DR; ASTRO-CM Study Team. Efficacy of adjunctive sertraline for the treatment of HIV-associated cryptococcal meningitis: an open-label dose-ranging study. Lancet Infect Dis. 2016 Jul;16(7):809-818. doi: 10.1016/S1473-3099(16)00074-8. Epub 2016 Mar 10.
Results Reference
background
PubMed Identifier
22508310
Citation
Zhai B, Wu C, Wang L, Sachs MS, Lin X. The antidepressant sertraline provides a promising therapeutic option for neurotropic cryptococcal infections. Antimicrob Agents Chemother. 2012 Jul;56(7):3758-66. doi: 10.1128/AAC.00212-12. Epub 2012 Apr 16.
Results Reference
background
PubMed Identifier
26324276
Citation
Smith KD, Achan B, Hullsiek KH, McDonald TR, Okagaki LH, Alhadab AA, Akampurira A, Rhein JR, Meya DB, Boulware DR, Nielsen K; ASTRO-CM/COAT Team. Increased Antifungal Drug Resistance in Clinical Isolates of Cryptococcus neoformans in Uganda. Antimicrob Agents Chemother. 2015 Dec;59(12):7197-204. doi: 10.1128/AAC.01299-15. Epub 2015 Aug 31.
Results Reference
background
PubMed Identifier
31345462
Citation
Rhein J, Huppler Hullsiek K, Tugume L, Nuwagira E, Mpoza E, Evans EE, Kiggundu R, Pastick KA, Ssebambulidde K, Akampurira A, Williams DA, Bangdiwala AS, Abassi M, Musubire AK, Nicol MR, Muzoora C, Meya DB, Boulware DR; ASTRO-CM team. Adjunctive sertraline for HIV-associated cryptococcal meningitis: a randomised, placebo-controlled, double-blind phase 3 trial. Lancet Infect Dis. 2019 Aug;19(8):843-851. doi: 10.1016/S1473-3099(19)30127-6.
Results Reference
result
PubMed Identifier
33677986
Citation
Lofgren SM, Nicol MR, Kandole TK, Castillo-Mancilla J, Anderson PL, Mpoza E, Tugume L, Bangdiwala AS, Ssebambulidde K, Hullsiek KH, Rhein J, Meya DB, Boulware DR. Short Communication: A Descriptive Analysis of Dried Blood Spot Adherence Testing Among Ugandans with HIV Presenting with Cryptococcal Meningitis. AIDS Res Hum Retroviruses. 2021 Jul;37(7):529-533. doi: 10.1089/AID.2020.0202. Epub 2021 Apr 12.
Results Reference
derived
PubMed Identifier
32843994
Citation
Kwizera R, Sadiq A, Ndyetukira JF, Nalintya E, Williams D, Rhein J, Boulware DR, Meya DB; COAT and ASTRO trial teams. Impact of community engagement and social support on the outcomes of HIV-related meningitis clinical trials in a resource-limited setting. Res Involv Engagem. 2020 Aug 20;6:49. doi: 10.1186/s40900-020-00228-z. eCollection 2020.
Results Reference
derived
PubMed Identifier
31242860
Citation
Ahimbisibwe C, Kwizera R, Ndyetukira JF, Kugonza F, Sadiq A, Hullsiek KH, Williams DA, Rhein J, Boulware DR, Meya DB. Management of amphotericin-induced phlebitis among HIV patients with cryptococcal meningitis in a resource-limited setting: a prospective cohort study. BMC Infect Dis. 2019 Jun 26;19(1):558. doi: 10.1186/s12879-019-4209-7.
Results Reference
derived
PubMed Identifier
30345376
Citation
Atherton RR, Ellis J, Cresswell FV, Rhein J, Boulware DR. Ophthalmic signs in Ugandan adults with HIV-associated cryptococcal meningitis: A nested analysis of the ASTRO-CM cohort. Wellcome Open Res. 2018 Oct 12;3:80. doi: 10.12688/wellcomeopenres.14666.2. eCollection 2018.
Results Reference
derived
PubMed Identifier
30325463
Citation
Tugume L, Rhein J, Hullsiek KH, Mpoza E, Kiggundu R, Ssebambulidde K, Schutz C, Taseera K, Williams DA, Abassi M, Muzoora C, Musubire AK, Meintjes G, Meya DB, Boulware DR; COAT and ASTRO-CM teams. HIV-Associated Cryptococcal Meningitis Occurring at Relatively Higher CD4 Counts. J Infect Dis. 2019 Feb 23;219(6):877-883. doi: 10.1093/infdis/jiy602.
Results Reference
derived
PubMed Identifier
30256903
Citation
Ssebambulidde K, Bangdiwala AS, Kwizera R, Kandole TK, Tugume L, Kiggundu R, Mpoza E, Nuwagira E, Williams DA, Lofgren SM, Abassi M, Musubire AK, Cresswell FV, Rhein J, Muzoora C, Hullsiek KH, Boulware DR, Meya DB; Adjunctive Sertraline for Treatment of HIV-associated Cryptococcal Meningitis Team. Symptomatic Cryptococcal Antigenemia Presenting as Early Cryptococcal Meningitis With Negative Cerebral Spinal Fluid Analysis. Clin Infect Dis. 2019 May 30;68(12):2094-2098. doi: 10.1093/cid/ciy817.
Results Reference
derived
Links:
URL
http://www.idi-makerere.com/
Description
Infectious Disease Institute
URL
http://www.accordiafoundation.org
Description
Accordia Global Health Foundation

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Adjunctive Sertraline for the Treatment of HIV-Associated Cryptococcal Meningitis

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