Bedaquiline-Pretomanid-Linezolid (BPaL) Regimen

Treatment for Multidrug Resistant Tuberculosis Without Extensive Drug Resistance

Typical Dosage: Bedaquiline 400mg daily for 2 weeks, then 200mg 3x/week for 22 weeks; Pretomanid 200mg daily; Linezolid 600mg daily (often reduced to 300mg daily)

Effectiveness
90%
Safety Score
55%
Clinical Trials
8
Participants
650

Comparative Safety Scale(Higher is safer)

Cyanide☠️
Meth💀
Cigarettes🚬
Chemo☢️
Alcohol🍺
Morphine💊
Antibiotics💉
Tylenol💊
Exercise🏃
Water💧
55
DangerousModerateSafe
Treatment Details
Dosage Range
Bedaquiline 400mg daily for 2 weeks, then 200mg 3x/week for 22 weeks; Pretomanid 200mg daily; Linezolid 600mg daily (often reduced to 300mg daily)
Time to Effect
2-4 weeks for initial response, 2-3 months for culture conversion
Treatment Duration
6 months
Evidence Quality
HIGH
Confidence Score
85%confidence in effectiveness data
Health Economics
Annual Cost of Care
Drug Cost:$15,000
Monitoring:$3,000
Side Effect Mgmt:$2,000
Total Annual:$20,000
Cost-Effectiveness Analysis
Cost-Effectiveness Rating
GOOD
ICER
$75,000/QALY
QALYs Gained
0.8
Outcome-Based Costs
Cost per Responder
$21,739
Cost per Remission
$22,727
Comparison vs Conventional longer MDR-TB regimen
Cost Difference
$-5,000/year
Less expensive
QALY Difference
+0.10 QALYs
Better outcomes
Dominance
DOMINATESBetter + cheaper
Bedaquiline-Pretomanid-Linezolid (BPaL) Regimen Outcomes

for Multidrug Resistant Tuberculosis Without Extensive Drug Resistance

Efficacy Outcomes
Overall Effectiveness
+90%
Response Rate
+92%
Remission Rate
+88%
Common Side Effects
Peripheral neuropathy (Linezolid)
+55%
Myelosuppression (Linezolid)
+15%
QT prolongation (Bedaquiline)
+15%
Nausea/Vomiting
+25%

WARNING: LIMITED TRIALS AVAILABLE

You can search for trials, but you probably can't join any because the 1% Treaty hasn't passed yet. Most trials are severely limited by lack of funding and bureaucratic barriers. Help change this!

Active Clinical Trials
No active trials currently recruiting for this treatment

No active trials found in ClinicalTrials.gov