Testing New Strategies for Patients Hospitalised With HIV-associated Disseminated Tuberculosis

Overview

The New Strat-TB trial is a superiority Phase III randomised control clinical trial with a 2X2 factorial design. The main aim of the study is to assess the efficacy and safety of high dose rifampicin and levofloxacin for 14 days in addition to standard TB therapy with or without steroids among adults hospitalized with HIV-associated disseminated tuberculosis. The investigators hypothesize that intensified treatment with increased rifampicin doses at 35 mg/kg plus levofloxacin will more rapidly reduce the mycobacterial load. The investigators also hypothesize that steroids will have an immune-modulatory effect and dampen the activation of the innate immune system. The investigators hypothesize that these two strategies will lead to improved survival in patients hospitalized with HIV-associated disseminated tuberculosis.

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Factorial Assignment
    • Primary Purpose: Treatment
    • Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
  • Study Primary Completion Date: June 30, 2024

Detailed Description

Primary efficacy endpoint: All-cause mortality at 12 weeks Secondary efficacy endpoint: All-cause mortality at 2 and 24 weeks Safety and tolerability endpoints: – Occurrence of hepatotoxicity using the American Thoracic Society (ATS) hepatotoxicity criteria: Alanine aminotransferase (ALT) elevation of more than three times the upper limit of normal (ULN) in the presence of hepatitis symptoms and/or jaundice or five times the upper limit of normal in the absence of symptoms. – Corticosteroid-associated adverse events, classified by severity and relation to study drug and will be reported if these develop within 4 weeks of enrolment. These will include new hypertension, new poor blood pressure control in a known hypertensive, hyperglycaemia, hypomania, mania, depression, acne, gastritis symptoms, upper gastrointestinal bleeding, and avascular bone necrosis. – Laboratory safety data (Grade 3 and 4 abnormalities using the ACTG grading system): liver function tests (alanine and aspartate aminotransferase[ALT, AST], gammaglutamyl transferase [GGT], alkaline phosphatase [ALP], International Normalized Ratio [INR], conjugated and total bilirubin [CBR, TBR]), glucose, full blood counts (including white cell, neutrophil and platelet counts plus haemoglobin) and electrolytes (sodium, potassium) and creatinine. – Occurrence of other opportunistic infections (AIDS-related, bacterial, fungal and viral) and malignancies (Kaposi's sarcoma) up to 12 weeks. – Occurrence of paradoxical tuberculosis immune reconstitution inflammatory syndrome (TB-IRIS) in patients starting antiretroviral therapy up to 12 weeks. – All grade 3 and 4 clinical adverse events (using the ACTG grading system) – Serious adverse events – Adverse events requiring study drug interruption and or withdrawal – Adverse drug reactions attributed to study drug Follow-up: Participants will be followed up daily while admitted to hospital for assessment of adverse events. Safety and routine blood tests will be done on day 2, 4, 7, 14 and 28. Further visits will be on week 12 and 24. Data monitoring: The trial will be monitored by an independent Data and Safety Monitoring Board (DSMB) comprising 4 independent researchers and an independent statistician. If there is evidence of harm related to study medication or trial conduct the DSMB may advise the sponsor that trial enrolment should be stopped. Clinical trial site: Mitchells Plain Hospital and Khayelitsha Hospital

Interventions

  • Drug: Rifampin
    • Rifampicin up to 35 mg/kg/day for 14 days
  • Drug: Levofloxacin
    • Levofloxacin 750mg daily (for weight <50kg) or 1 g daily (for weight >50 kg) daily for 14 days
  • Drug: Rifampicin, Pyrazinamide, Ethambutol and Isoniazid
    • Rifampicin 10 mg/kg; Isoniazid 5 mg/kg; Pyrazinamide 15 mg/kg; Ethambutol15 mg/kg in fixed dose combination administered per weight band. Standard of care control arm
  • Drug: Prednisone
    • Prednisone 1.5mg/kg/day for 14 days
  • Drug: Placebo
    • Placebo identical to Prednisone

Arms, Groups and Cohorts

  • Experimental: High dose Rifampicin plus Levofloxacin
    • Standard TB treatment plus additional Rifampicin 35 mg/kg/day PLUS Levofloxacin for 14 days
  • Experimental: Prednisone
    • Prednisone 1.5 mg/kg for 14 days
  • Active Comparator: Standard TB treatment
    • High dose rifampicin/levofloxacin comparator
  • Placebo Comparator: Placebo
    • Prednisone comparator

Clinical Trial Outcome Measures

Primary Measures

  • All-cause mortality
    • Time Frame: 12 weeks

Secondary Measures

  • In-hospital mortality during index admission
    • Time Frame: 7 days
  • All-cause mortality
    • Time Frame: 2 and 24 weeks respectively

Participating in This Clinical Trial

Inclusion Criteria

  • Aged >18 – HIV infection – Disseminated TB confirmed by one or more of the following tests being positive 1. Lysed blood Xpert Ultra positive for MTB 2. Concentrated urine Xpert Ultra positive for MTB 3. Urine Alere LAM positive – Hospital clinical team made decision to initiate TB treatment Exclusion Criteria:

  • Pregnant or breastfeeding – Active or recent SARS-CoV-2 infection – TB treatment within the last 1 month or more than 2 doses of TB treatment – Rifampicin resistance – Neurological TB – Receiving corticosteroids or other immunosuppressive therapy – ALT >120 IU/L or total bilirubin >34 ╬╝mol/L – Plasma CrAg positive or cryptococcal meningitis – Current malignancy requiring active treatment (including any Kaposi sarcoma lesions) – Patients established on ART with Protease Inhibitor based regimen who cannot be switched to a dolutegravir based regimen – Diabetic ketoacidosis or Hyperosmolar Non-ketotic acidosis – Any condition in the opinion of the investigator for which participation would increase risk to the patient

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • University of Cape Town
  • Provider of Information About this Clinical Study
    • Principal Investigator: Charlotte Schutz, Co-Principal Investigator – University of Cape Town
  • Overall Contact(s)
    • Charlotte Schutz, PhD, +27 (0)21 406 6797, charlotte.schutz@uct.ac.za

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