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Cryptococcal Antigen Screening Plus Sertraline (C-ASSERT)

Primary Purpose

Cryptococcosis, Cryptococcal Infections, AIDS-Related Opportunistic Infections

Status
Terminated
Phase
Phase 3
Locations
Uganda
Study Type
Interventional
Intervention
Sertraline
Placebo Oral Tablet
Fluconazole
Sponsored by
University of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cryptococcosis focused on measuring cryptococcal antigen, preemptive treatment, CRAG+, sertraline, fluconazole, randomized clinical trial, HIV

Eligibility Criteria

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

Inclusion Criteria:

  • HIV-infected
  • Cryptococcal antigen (CrAg) positive in blood
  • Age >=18 years
  • Written informed consent
  • Women of childbearing potential who are participating in sexual activity that could lead to pregnancy must agree to use one reliable method of contraception while receiving fluconazole >=400mg/day

Exclusion Criteria:

  • Prior history of cryptococcal meningitis
  • Suspected meningitis or mania
  • Suspected/known cirrhosis, jaundice, or alanine aminotransferase (ALT) >5x upper limit of normal
  • Receiving an antidepressant medicine
  • Receiving antifungal therapy, >1 week
  • Pregnant or Breastfeeding
  • Contraindication to sertraline or fluconazole
  • Current rifampin use or other prohibited medication
  • Electrocardiogram corrected QT interval (QTc) >450ms

Sites / Locations

  • Infectious Disease Institute, Makerere University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Sertraline

Control

Arm Description

Fluconazole Standard of Care + Sertraline

Fluconazole Standard of Care + Placebo Oral Tablet

Outcomes

Primary Outcome Measures

6 Month Meningitis-free Survival
Cryptococcal meningitis free survival with retention-in-care through 6 months Those who die of any cause are failures Those developing symptomatic cryptococcal meningitis are failures Those lost to follow up and unable to be tracked are considered failures

Secondary Outcome Measures

6-month Survival
Survival through 6 months
Cumulative Incidence of Symptomatic Cryptococcal Meningoencephalitis
Cumulative incidence of symptomatic cryptococcal meningoencephalitis through 6 months
Number of Clinical Adverse Events (Grade 3-5)
Number of Clinical Adverse Events by Division of AIDS (DAIDS) Scale for Grade 3-5 events through 6 months
Number of Laboratory Grade 3-5 Adverse Events
Number of Laboratory Grade 3-5 Adverse Events through 6 months as per the Division of AIDS (DAIDS) grading scale
All-Cause Premature Study Drug/Placebo Discontinuation
Number of participants whose study drug/placebo use was halted prematurely due to any cause through 6 months
Prevalence of Depression by Patient Health Questionnaire (PHQ-9) Over Time
Prevalence of depression by Patient Health Questionnaire (PHQ-9) over 6 months as measured at baseline, 4 weeks, 8 weeks, and 12 weeks. The PHQ-9 is a 9-item instrument for screening, diagnosing, monitoring, and measuring the severity of depression. Items are rated on a scale from 0 (not at all) to 3 (nearly every day). Total score is a sum of 9 item scores (Range 0-27). Greater scores indicate greater depressive symptoms. PHQ-9 scores of: 0-4 Minimal/No depression; 5-9 Mild depression; 10-14 Moderate depression; 15-19 Moderate severe depression; 20-27 Severe depression. This endpoint reports the median (interquartile range) of the PHQ-9 scores over time.

Full Information

First Posted
December 14, 2016
Last Updated
June 2, 2020
Sponsor
University of Minnesota
Collaborators
Infectious Diseases Institute, Uganda, National Institute of Allergy and Infectious Diseases (NIAID), Mbarara University of Science and Technology
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1. Study Identification

Unique Protocol Identification Number
NCT03002012
Brief Title
Cryptococcal Antigen Screening Plus Sertraline
Acronym
C-ASSERT
Official Title
Cryptococcal Antigen Screening Plus Sertraline
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Terminated
Why Stopped
SAEs with n=1 serotonin syndrome, n=2 SAEs after sertraline interruption.
Study Start Date
November 15, 2017 (Actual)
Primary Completion Date
March 13, 2018 (Actual)
Study Completion Date
March 13, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
Collaborators
Infectious Diseases Institute, Uganda, National Institute of Allergy and Infectious Diseases (NIAID), Mbarara University of Science and Technology

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Cryptococcal meningitis or "Crypto" is a life threatening fungal infection around the brain that requires hospitalization for treatment for 14 days and then continued therapy. Crypto causes 15-20% of HIV/AIDS-related deaths worldwide. However, this infection can be detected before one develops symptoms and becomes ill. People can be screened for infection by a blood test to detect "cryptococcal antigen," (called CrAg), which is part of the fungus, in blood. The World Health Organization and over 22 countries worldwide recommend CrAg screening of all persons with advanced AIDS entering or re-entering into HIV care. However, it is not known how best to treat people with cryptococcal antigen in their blood, who don't otherwise yet have symptoms of infection around their brain. If no treatment is given, almost all people will develop infection of the brain and/or die. International guidelines suggest using both HIV medicines and an anti-fungal medicine, called fluconazole, to treat this early infection. However, despite this treatment approximately 1 in 4 people may get sick and/or die. Researchers have recently discovered another medicine that may work against the Cryptococcus fungus. This medicine is called Sertraline, and it is actually a medicine that has been used for more than 25 years to treat depression (sadness). Sertraline is one of the most commonly used medicines worldwide. The purpose of this research clinical trial is to determine if standard fluconazole antifungal therapy plus a high dose of Sertraline, will be better than standard fluconazole therapy alone for treating early disseminated cryptococcal infection in persons who are asymptomatic and do not yet have infection of the brain (i.e. meningitis). This study seeks to test if Sertraline will improve survival through 6-months. Prior studies have shown that >90% of those who survive 6-months will survive >5 years.
Detailed Description
This is a double-blind, randomized placebo-controlled clinical trial testing sertraline as an antifungal medicine in combination with fluconazole for treatment of HIV-infected persons with AIDS and asymptomatic cryptococcal antigenemia (CrAg+).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cryptococcosis, Cryptococcal Infections, AIDS-Related Opportunistic Infections
Keywords
cryptococcal antigen, preemptive treatment, CRAG+, sertraline, fluconazole, randomized clinical trial, HIV

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Sertraline
Arm Type
Experimental
Arm Description
Fluconazole Standard of Care + Sertraline
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Fluconazole Standard of Care + Placebo Oral Tablet
Intervention Type
Drug
Intervention Name(s)
Sertraline
Other Intervention Name(s)
Zoloft, Lustral, Sertraline hydrochloride
Intervention Description
sertraline 400mg/day
Intervention Type
Drug
Intervention Name(s)
Placebo Oral Tablet
Other Intervention Name(s)
Placebo
Intervention Description
matched placebo tablet
Intervention Type
Drug
Intervention Name(s)
Fluconazole
Other Intervention Name(s)
Fluconazole 200mg tab
Intervention Description
Standard of Care Fluconazole per World Health Organization and Ugandan Guidelines (800mg/day x 2 weeks, 400mg/day x10 weeks, 200mg through 6 months).
Primary Outcome Measure Information:
Title
6 Month Meningitis-free Survival
Description
Cryptococcal meningitis free survival with retention-in-care through 6 months Those who die of any cause are failures Those developing symptomatic cryptococcal meningitis are failures Those lost to follow up and unable to be tracked are considered failures
Time Frame
6 months
Secondary Outcome Measure Information:
Title
6-month Survival
Description
Survival through 6 months
Time Frame
6 months
Title
Cumulative Incidence of Symptomatic Cryptococcal Meningoencephalitis
Description
Cumulative incidence of symptomatic cryptococcal meningoencephalitis through 6 months
Time Frame
6 months
Title
Number of Clinical Adverse Events (Grade 3-5)
Description
Number of Clinical Adverse Events by Division of AIDS (DAIDS) Scale for Grade 3-5 events through 6 months
Time Frame
6 months
Title
Number of Laboratory Grade 3-5 Adverse Events
Description
Number of Laboratory Grade 3-5 Adverse Events through 6 months as per the Division of AIDS (DAIDS) grading scale
Time Frame
6 months
Title
All-Cause Premature Study Drug/Placebo Discontinuation
Description
Number of participants whose study drug/placebo use was halted prematurely due to any cause through 6 months
Time Frame
6 months
Title
Prevalence of Depression by Patient Health Questionnaire (PHQ-9) Over Time
Description
Prevalence of depression by Patient Health Questionnaire (PHQ-9) over 6 months as measured at baseline, 4 weeks, 8 weeks, and 12 weeks. The PHQ-9 is a 9-item instrument for screening, diagnosing, monitoring, and measuring the severity of depression. Items are rated on a scale from 0 (not at all) to 3 (nearly every day). Total score is a sum of 9 item scores (Range 0-27). Greater scores indicate greater depressive symptoms. PHQ-9 scores of: 0-4 Minimal/No depression; 5-9 Mild depression; 10-14 Moderate depression; 15-19 Moderate severe depression; 20-27 Severe depression. This endpoint reports the median (interquartile range) of the PHQ-9 scores over time.
Time Frame
12 weeks
Other Pre-specified Outcome Measures:
Title
Adherence to Study Drug
Description
Participants' percent adherence to study drug regiment by pharmacy medication counts, representing the percent of the total prescribed medication taken by participants.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV-infected Cryptococcal antigen (CrAg) positive in blood Age >=18 years Written informed consent Women of childbearing potential who are participating in sexual activity that could lead to pregnancy must agree to use one reliable method of contraception while receiving fluconazole >=400mg/day Exclusion Criteria: Prior history of cryptococcal meningitis Suspected meningitis or mania Suspected/known cirrhosis, jaundice, or alanine aminotransferase (ALT) >5x upper limit of normal Receiving an antidepressant medicine Receiving antifungal therapy, >1 week Pregnant or Breastfeeding Contraindication to sertraline or fluconazole Current rifampin use or other prohibited medication Electrocardiogram corrected QT interval (QTc) >450ms
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elizabeth K Nalintya, MBChB MPH
Organizational Affiliation
Infectious Disease Institute
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Radha Rajasingham, MD
Organizational Affiliation
University of Minnesota
Official's Role
Study Director
Facility Information:
Facility Name
Infectious Disease Institute, Makerere University
City
Kampala
ZIP/Postal Code
22418
Country
Uganda

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
A formal written data sharing plan exists. Protocol and trial documents can be shared. De-identified data can be shared after trial completion.
IPD Sharing Time Frame
Available for at least 5 years
IPD Sharing Access Criteria
Upon request to the Principal Investigator
Citations:
PubMed Identifier
32415846
Citation
Boulware DR, Nalintya E, Rajasingham R, Kirumira P, Naluyima R, Turya F, Namanda S, Rutakingirwa MK, Skipper CP, Nikweri Y, Hullsiek KH, Bangdiwala AS, Meya DB. Adjunctive sertraline for asymptomatic cryptococcal antigenemia: A randomized clinical trial. Med Mycol. 2020 Nov 10;58(8):1037-1043. doi: 10.1093/mmy/myaa033.
Results Reference
result
Links:
URL
http://preventcrypto.org
Description
PreventCrypto.org has information and training materials for cryptococcal antigen screening and treatment
URL
http://www.gaffi.org/
Description
Global Action Fund for Fungal Infections (GAFFI)

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Cryptococcal Antigen Screening Plus Sertraline

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