Pharmacokinetic Study of Linezolid for TB Meningitis

Tuberculosis, Meningeal Clinical Trial

— SIMPLE  

Official title:

Short Intervention and Measurement of Pharmacokinetics of Linezolid in Tuberculosis Meningitis: a Pharmacokinetics and Safety/Tolerability Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03537495
• Other study ID #: TB-201805.01
• Status: Completed
• Phase: Phase 2
• Start date: June 21, 2021
• Est. completion date: July 20, 2023

Study information

• Verified date: September 2023
• Source: Universitas Padjadjaran
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Tuberculosis meningitis (TBM) is the most severe manifestation of TB, resulting in death or neurological disability in up to 50% of affected patients, despite antibacterial treatment. This TBM treatment follows the model for pulmonary TB by using the same first-line TB drugs (a combination of rifampicin, isoniazid, pyrazinamide and ethambutol) and the same dosing guidelines, although it is known that penetration of two of these drugs (rifampicin and ethambutol) into cerebrospinal fluid (CSF) is limited. Improvement of treatment of TBM is urgently needed.

To do so, a combination of two interventions will be investigated in this study. A series of phase II clinical trials on higher doses of the pivotal TB drug rifampicin in Indonesian patients with TBM have shown that the dose of rifampicin can be increased from 10 mg/kg orally (standard dose) up to 30 mg/kg orally, resulting in a strong increase in exposure to this drug in plasma and CSF, no increase in grade III or IV adverse effects, and a reduction in mortality. Similarly, higher doses of rifampicin up to 35 mg/kg resulted in strong increases in plasma concentrations; the doses were well tolerated and reduced time to sputum conversion in African pulmonary TB patients.

Next to a higher dose of rifampicin, the approved antibacterial drug linezolid seems a good candidate for a new TBM regimen. The drug penetrates well into the CSF and is applied successfully against other central nervous system (CNS) infections (e.g. caused by penicillin-nonsusceptible Streptococcus pneumoniae, vancomycin-resistant enterococci and methicillin-resistant Staphylococcus aureus). In a study in China, linezolid in a dose of 600 mg BID orally strongly increased recovery of patients with TBM response. Linezolid is also being investigated as a new drug for (drug-resistant) pulmonary TB in numerous studies, in a dose of 1200 mg once daily. More severe adverse effects to this drug typically occur only after prolonged treatment during several months, not during short-term treatment.

Overall, linezolid is expected to be a promising and tolerable candidate for a new intensified TBM treatment regimen consisting of a backbone of high dose rifampicin plus linezolid.

Description:

Overall aim is to determine the most appropriate dose of linezolid in the treatment of TB meningitis, when combined with high-dose rifampicin (35 mg/kg orally), to be tested in larger clinical follow-up studies.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 36
• Est. completion date: July 20, 2023
• Est. primary completion date: March 1, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age: 18 years old or older

• Clinically diagnosed as TB meningitis patient

• CSF/blood glucose ratio < 0.5

• Willing to participate in the study by signing informed consent

Exclusion Criteria:

Patients who have one of the following criteria will be excluded:

• Failure to diagnostic lumbar puncture

• Confirmed cryptococcus meningitis (LFA) in HIV-positive patients; or diagnosed as bacterial meningitis based on clinical assessment and routine CSF examination.

• Treatment for tuberculosis for more than 3 days before admission

• History of TBM

• Current treatment with: MAO inhibitors, direct and indirect acting sympathomimetic drugs, vasopressive drugs, dopaminergic compounds, buspiron, serotonin reuptake inhibitors, tricyclic antidepressants, triptans, tramadol and meperidine

• History (< 2 weeks before start of linezolid) of taking any MAO inhibitors

• Pregnant or lactating females

• Hepatic insufficiency (ALT>5x upper normal limit)

• Kidney dysfunction (eGFR <50ml/min)

• Known hypersensitivity to rifampicin and/or linezolid

• Rapid clinical deterioration at time of presentation (sepsis, decreasing consciousness, or signs of cerebral oedema or herniation)

Related Conditions & MeSH terms

• Linezolid
• Meningitis
• Tuberculosis
• Tuberculosis, Meningeal

Intervention

Drug:
• Linezolid
Overall, there is an urgent need for improvement of TBM treatment. LInezolid is known to be well-penetrated to blood brain barrier. A combination of high-dose rifampicin and linezolid as an intensified add-on therapy in the management of TB meningitis has never been studied. The goal is to assess the most appropriate dose of linezolid for larger follow-up studies and to evaluate the feasibility of a linezolid-containing TBM regimen.

Locations

Country	Name	City	State
Indonesia	Hasan Sadikin General Hospital	Bandung	Jawa Barat

Sponsors (3)

Lead Sponsor	Collaborator
Universitas Padjadjaran	Global Alliance for TB Drug Development, Radboud University Medical Center

Country where clinical trial is conducted

Indonesia, 

References & Publications (2)

Dian S, Yunivita V, Ganiem AR, Pramaesya T, Chaidir L, Wahyudi K, Achmad TH, Colbers A, Te Brake L, van Crevel R, Ruslami R, Aarnoutse R. Double-Blind, Randomized, Placebo-Controlled Phase II Dose-Finding Study To Evaluate High-Dose Rifampin for Tuberculous Meningitis. Antimicrob Agents Chemother. 2018 Nov 26;62(12):e01014-18. doi: 10.1128/AAC.01014-18. Print 2018 Dec. — View Citation

Ruslami R, Ganiem AR, Dian S, Apriani L, Achmad TH, van der Ven AJ, Borm G, Aarnoutse RE, van Crevel R. Intensified regimen containing rifampicin and moxifloxacin for tuberculous meningitis: an open-label, randomised controlled phase 2 trial. Lancet Infect Dis. 2013 Jan;13(1):27-35. doi: 10.1016/S1473-3099(12)70264-5. Epub 2012 Oct 25. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Linezolid exposure in blood and CSF	Linezolid exposure in blood (full plasma concentration-versus-time profiles (0-24h)) will be measured in 2 days, i.e. day 2 (+/- 1) and at day 11 (+/- 1) of TB treatment. In each sampling day, there will be 6 sampling points i.e. at 0 (pre-dose), 1, 2, 4, 8, and 12 h after study medication intake; One CSF sample per patient will be taken at the same day as PK sampling i.e. at 2, 4 or 8 hours post dose.	day 2 and day 11
Secondary	Serious adverse event	Serious adverse events assessed daily during the 14 days of intensified treatment (e.g. gastro-intestinal intolerance), and grade 1-4 adverse events (e.g. liver function and hematology) assessed at day 3, 7, 10 and 14.	Day 3, 7, 10 and 14
Secondary	Clinical response	Clinical response includes resolution of fever, resolution of hyponatremia etc.	Day 3, 7 and 14.
Secondary	Neurological response	Neurological response includes resolution of consciousness, development of raised intracranial pressure, etc.	Day 3, 7 and 14.
Secondary	Mortality	mortality during the first month will be recorded and cause of death will be classified as neurologic or non-neurologic, if applicable	Within 14 days and 1 month after starting treatment
Secondary	Blood inflammatory response	Profile of inflammatory response in blood	at PK days (day 2 and 11), and day 7 and 14
Secondary	CSF inflammatory response	inflammatory response in CSF at PK sampling days	at PK sampling days (day 2 and 11)