From Tuberculosis › Chapter 16: Treatment of latent tuberculosis infection · Médecins Sans Frontières, Current online edition, 2026
MSF guidance on choosing and dosing regimens for latent TB treatment in children, adolescents and adults.
- Issuer
- Médecins Sans Frontières
- Edition
- Current online edition, 2026
- Audience
- Clinicians and public health professionals managing tuberculosis prevention
- Evidence
- WHO recommendations and clinical trial evidence
- Reviewed
- 23 Oct 2026 · GMJ
What this guideline says
GMJ summary
Médecins Sans Frontières recommends three primary regimens for latent tuberculosis infection (LTBI): isoniazid monotherapy for 6 months (6H) or 36 months in specific populations (36H); isoniazid plus rifapentine weekly for 3 months (3HP); or isoniazid plus rifampicin daily for 3 months (3HR). Two alternative regimens are also available: isoniazid plus rifapentine daily for 1 month (1HP) for those aged ≥13 years, and rifampicin monotherapy for 4 months (4R).
The choice of regimen depends on the drug susceptibility of the source case, co-morbidities including HIV infection, risk of drug interactions (especially with antiretrovirals), treatment duration, likelihood of adherence, and individual patient characteristics such as age and pregnancy status. Shorter regimens (3HP, 3HR, 1HP) generally have higher completion rates than 6-month isoniazid monotherapy, though rifapentine-containing regimens are not currently recommended for pregnant women.
Persons at risk of peripheral neuropathy should receive pyridoxine (vitamin B6) throughout isoniazid treatment. Rifamycin-containing regimens have significant drug interactions, particularly with antiretrovirals and contraceptives, and pregnant women taking rifampicin should receive phytomenadione (vitamin K) in the final weeks of pregnancy.
Key points
For clinicians — doses and thresholds as stated in the guideline
- Isoniazid monotherapy: <30 kg receive 10 mg/kg (7–15 mg/kg) once daily, ≥30 kg receive 5 mg/kg (4–6 mg/kg) once daily (maximum 300 mg daily) for 6 months (or 36 months in some HIV-positive populations)
- 3HP regimen (weekly for 3 months): isoniazid 20–30 mg/kg (<30 kg, ≥2 years) or 900 mg (≥30 kg) plus rifapentine 300–900 mg based on weight bands; recommended for children ≥2 years, adolescents and adults regardless of HIV status
- 3HR regimen (daily for 3 months): isoniazid and rifampicin at standard doses; recommended for all ages including pregnant women, with fixed-dose combinations available
- 1HP regimen (daily for 1 month, alternative): isoniazid 300 mg plus rifapentine 600 mg for those ≥13 years; high completion rate but cutaneous reactions common
- 4R regimen (daily for 4 months, alternative): rifampicin monotherapy at 15 mg/kg (<30 kg) or 10 mg/kg (≥30 kg), maximum 600 mg daily; better safety profile than 6H but risk of rifampicin resistance if active TB undiagnosed
- Pyridoxine (vitamin B6) should be given to all persons at risk of peripheral neuropathy receiving isoniazid for the entire treatment duration
- Rifapentine-containing regimens are not currently recommended for pregnant women; 3HR and 4R regimens are safe in pregnancy with phytomenadione (vitamin K) in late pregnancy
- Hypersensitivity reactions occur in approximately 4% of patients on 3HP and 2% on 3HR; rifamycin regimens have significant drug interactions with antiretrovirals and contraceptives
LTBI treatment regimens
Table extracted from the guideline
| Regimen | Drug | Dosing |
|---|---|---|
| 6H or 36H (recommended) | Isoniazid PO daily | <30 kg: 10 mg/kg (7–15 mg/kg); ≥30 kg: 5 mg/kg (4–6 mg/kg); max. 300 mg daily |
| 3HP (recommended) | Isoniazid PO weekly | <30 kg, ≥2 years: 20–30 mg/kg; ≥30 kg: 900 mg |
| 3HP (recommended) | Rifapentine PO weekly | 10–14 kg: 300 mg; 14.1–25 kg: 450 mg; 25.1–32 kg: 600 mg; 32.1–49.9 kg: 750 mg; ≥50 kg: 900 mg |
| 3HR (recommended) | Isoniazid PO daily | <30 kg: 10 mg/kg (7–15 mg/kg); ≥30 kg: 5 mg/kg (4–6 mg/kg); max. 300 mg daily |
| 3HR (recommended) | Rifampicin PO daily | <30 kg: 15 mg/kg; ≥30 kg: 10 mg/kg; max. 600 mg daily |
| 1HP (alternative, ≥13 years) | Isoniazid PO daily | 300 mg |
| 1HP (alternative, ≥13 years) | Rifapentine PO daily | 600 mg |
| 4R (alternative) | Rifampicin PO daily | <30 kg: 15 mg/kg; ≥30 kg: 10 mg/kg; max. 600 mg daily |
Source: Médecins Sans Frontières, Latent tuberculosis infection treatment regimens — MSF Tuberculosis. Reproduced in summary form.
From the guideline
Verbatim
“The decision to prescribe one regimen rather than the other should take into consideration: Drug-susceptibility of the strain of the presumed source patient, if known.”
Editor’s perspective
Why this matters for Georgia and the region
Prof. Giorgi Pkhakadze, MD, MPH, PhD
Editor-in-Chief, Georgian Medical Journal · Chair, Public Health Institute of Georgia · WHO consultant, health and migration
As Georgia continues to strengthen its tuberculosis control programme within the universal health coverage framework, this MSF guidance offers practical alternatives to traditional isoniazid monotherapy that may significantly improve treatment completion rates. For Georgian clinicians, I would emphasise the 3HR regimen (3 months of daily isoniazid-rifampicin) as particularly suitable for our setting: it is shorter than 6-month isoniazid, has good evidence, fixed-dose combinations are available, and it can be used in all populations including pregnant women. However, national programmes must carefully consider the drug interaction profile of all rifamycin-containing regimens, particularly given the increasing number of patients co-infected with HIV who are on antiretroviral therapy; close collaboration between TB and HIV services is essential to safely implement these shorter regimens. The availability and cost of rifapentine in Georgia and neighbouring countries remains a barrier to implementing the 3HP and 1HP regimens, though these may become more accessible as global procurement mechanisms improve.
ORCID 0000-0001-7609-4515 · Perspective written for the GMJ Guidelines Library, 23 Oct 2026
Applicability
Georgia and the South Caucasus
Georgia has a moderate TB incidence and these MSF regimens align with WHO recommendations already adopted by the Georgian National TB Programme. The choice between regimens is particularly relevant given Georgia’s HIV prevalence and the need to consider antiretroviral interactions, especially in key populations. National TB programmes in the South Caucasus should evaluate the availability and cost of rifapentine (not yet widely available in the region) versus more established rifampicin-based regimens, assess the feasibility of directly observed weekly therapy for 3HP in rural settings, and ensure that fixed-dose combinations of 3HR are procured to improve adherence. The significant drug interactions between rifamycins and commonly used antiretrovirals require close coordination between TB and HIV services in countries like Georgia, Armenia and Azerbaijan.
Questions this guideline answers
Quick answers
Which LTBI regimen has the highest completion rate?
The shorter regimens—3HP (weekly for 3 months), 3HR (daily for 3 months), and 1HP (daily for 1 month)—all have higher completion rates than the traditional 6-month isoniazid monotherapy. The 1HP regimen (1 month daily treatment) has a particularly high completion rate, though it is only recommended for those aged 13 years and over.
Can rifapentine-based regimens be used in pregnant women?
No, rifapentine-containing regimens (3HP and 1HP) are not currently recommended for pregnant women. Despite some reassuring safety data, safety is not definitively established. Pregnant women can receive isoniazid monotherapy (6H), 3HR, or 4R regimens; those taking rifampicin should receive phytomenadione (vitamin K) in the last few weeks of pregnancy.
How do I choose between isoniazid monotherapy and combination regimens?
Consider drug susceptibility of the source case, co-morbidities (HIV, liver disease, neuropathy), drug interactions (especially with antiretrovirals and contraceptives), treatment duration, likelihood of adherence, age, pregnancy status, and programme considerations. Shorter combination regimens generally have better adherence but more drug interactions; isoniazid monotherapy is longer but simpler in patients on multiple medications.
Who needs pyridoxine supplementation during LTBI treatment?
All persons at risk of peripheral neuropathy should receive pyridoxine (vitamin B6) for the entire duration of isoniazid treatment. This includes individuals with diabetes, HIV infection, malnutrition, alcohol use disorder, chronic kidney disease, and pregnant or breastfeeding women. Dosing recommendations are provided in Appendix 17 of the MSF guideline.
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Quality & accreditation
Same guideline
- Treatment of latent tuberculosis infection — Introduction — MSF TuberculosisChapter 16: Treatment of latent tuberculosis infection
- BCG vaccination for staff exposed to tuberculosis — MSF TuberculosisChapter 15: Follow-up of staff exposed to tuberculosis
- Preventive measures at patients' homes — MSF TuberculosisChapter 14: Infection prevention and control
- Respiratory protection measures in health facilities — MSF TuberculosisChapter 14: Infection prevention and control
- Environmental Measures in Health Facilities — MSF TuberculosisChapter 14: Infection prevention and control
- Administrative measures in health facilities — MSF TuberculosisChapter 14: Infection prevention and control
Other guidelines on this topic
- Treatment of latent tuberculosis infection — Introduction — MSF Tuberculosis
- BCG vaccination for staff exposed to tuberculosis — MSF Tuberculosis
- Intrauterine foetal death — MSF Essential obstetric and newborn care
- Preventive measures at patients' homes — MSF Tuberculosis
- Threatened preterm delivery — MSF Essential obstetric and newborn care
- Issuer
- Médecins Sans Frontières
- Guideline
- Tuberculosis
- Chapter
- Chapter 16: Treatment of latent tuberculosis infection
- Type
- Clinical guideline (chapter)
- Edition
- Current online edition, 2026
- Status
- Current
- Published
- 2026-10-14
- Languages
- English, French
- Scope
- Treatment regimens for latent tuberculosis infection
- Audience
- Clinicians and public health professionals managing tuberculosis prevention
- Evidence
- WHO recommendations and clinical trial evidence
- Record history
- Created 23 Oct 2026 · updated 23 Oct 2026 · next check Apr 2027
Médecins Sans Frontières. 16.3 Latent tuberculosis infection treatment regimens. In: Tuberculosis. Paris: MSF; 2026 Oct 14. Available from: https://medicalguidelines.msf.org/en/viewport/TUB/english/GMJ Guidelines Library records are original summaries written by the GMJ editorial team from the issuer’s published document and reviewed by a physician. They do not replace the full guideline. The document is the copyright of its issuer and is linked, not hosted. Spotted an error or a newer edition? Tell the Guidelines Desk.
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