New drug duo takes on deadly brain infection
NCT ID NCT07350174
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new two-drug combination (Alpibectir and Ethionamide) added to standard treatment for tuberculosis meningitis, a serious brain infection. About 64 adults newly diagnosed with the condition will receive the drugs to see how well they reach the brain and how safe they are. The trial also checks how the drugs interact with HIV treatment in patients who are HIV-positive.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 64 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2028
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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15 to 64 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥ 15 years and \< 65 years 2. Diagnosis of TBM defined as "definite" or "probable", using criteria proposed by the Tuberculosis Meningitis International Research Consortium. * Definite TBM is defined by at least one of the following criteria: acid-fast bacilli (AFB) seen in CSF microscopy, positive CSF M. tuberculosis culture, or positive CSF M. tuberculosis commercial nucleic acid amplification test in the setting of symptoms suggestive of meningitis. * Probable TBM is defined using a modified Marais score\* Probable TBM: total score\* ≥ 12 when neuroimaging is available, or ≥ 10 when neuroimaging is not available. At least 2 points should come from CSF or 2 points from cerebral imaging criteria. (\*see Appendix 2: Modified Marais Score) 3. Informed consent signed by the patient. For patients with Glasgow Coma Scale (GCS) \< 15, the consent of a next of kin/relative will be required, in accordance with applicable local laws and regulations. Deferred consent will be obtained from the participant when their level of consciousness improves, and they have capacity to provide consent. For adolescents below the age of civil majority (as defined in each country), the consent of at least one parent or legal guardian and the assent of the adolescent will be required. Exclusion Criteria: 1. Having received \>14 days of HRZE TB treatment. 2. In people with HIV infection: use of antiretroviral treatment (ART) other than efavirenz- or dolutegravir-based. 3. Glasgow Coma Scale \< 10. 4. Body weight measured or estimated: \< 40 kg or \> 90 kg or BMI \> 40 kg/m2. 5. Renal failure (eGFR \< 30 mL/min, calculated by CKD-EPI formula). 6. Alanine aminotransferase (ALT) \> 5 times the Upper Limit of Normal. 7. Clinical evidence of liver failure or decompensated cirrhosis. 8. For women of childbearing potential, one or more of the following: 1. Being pregnant, breast-feeding, or intending to breast-feed or conceive a child during the study or within 30 days after the end of treatment visit (D56), OR; 2. Not willing or able to use highly effective contraceptive methods (as defined per Appendix 7) starting at screening and continuing until 30 days after the end of treatment visit (D56). 9. For male participants: intending to conceive a child or not willing or able to consistently use a barrier method e.g. condoms during all sexual activity from inclusion until 90 days after the end of treatment visit (D56). Note: Male participants should be advised of the benefit for a female partner to use a highly effective method of contraception as a condom may break or leak when having sexual intercourse. 10. Documented Mtb resistance to rifampicin. 11. Positive Gram-stain, bacterial culture other than Mtb or cryptococcal antigen in the CSF. 12. For HIV positive patients: Presence of cryptococcal antigen in the blood. 13. Inability to collect CSF or contraindication to lumbar puncture (LP).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.