DFDA

Clofazimine (as part of an optimized background regimen for MDR-TB)

Treatment for Hiv Aids Multidrug Resistant Tuberculosis Without Extensive Drug Resistance

Typical Dosage: 100-200mg daily or thrice weekly

Effectiveness
70%
Safety Score
70%
Clinical Trials
40
Participants
7K

Comparative Safety Scale(Higher is safer)

Cyanideâ˜ ī¸
Meth💀
CigarettesđŸšŦ
Chemoâ˜ĸī¸
AlcoholđŸē
Morphine💊
Antibiotics💉
Tylenol💊
Exercise🏃
Water💧
70
DangerousModerateSafe
Treatment Details
Dosage Range
100-200mg daily or thrice weekly
Time to Effect
2-4 months for clinical improvement
Treatment Duration
Clofazimine component 6-12 months, total regimen 9-18 months
Evidence Quality
MODERATE
Number Needed to Treat (NNT)
12(Treat 12 patients to see 1 additional successful outcome)
Number Needed to Harm (NNH)
15(Treat 15 patients to see 1 additional serious adverse event)
Confidence Score
78%confidence in effectiveness data
Health Economics
Annual Cost of Care
Drug Cost:$12,000
Monitoring:$2,000
Side Effect Mgmt:$1,000
Total Annual:$15,000
Cost-Effectiveness Analysis
Cost-Effectiveness Rating
EXCELLENT
ICER
$30,000/QALY
QALYs Gained
7
Outcome-Based Costs
Cost per Responder
$21,429
Cost per Remission
$21,429
Comparison vs Older MDR-TB regimens without Clofazimine
Cost Difference
$-5,000/year
Less expensive
QALY Difference
+0.30 QALYs
Better outcomes
Dominance
DOMINATESBetter + cheaper
Prescription Access Economics
Annual Societal Loss per Patient
$1,500
Cost of prescription-only barriers (visits, time, admin, price premium)
Physician Visit Cost
$480/year
Time Cost
$240/year
Travel + wait time
Insurance Admin Cost
$80/year
Prior auth, claims
Rx Price
$1,000/year
Potential OTC Price
$300/year
Estimated if OTC available
Risk Assessment
Misuse Risk
LOW
Missed Diagnosis Risk
LOW
Clofazimine (as part of an optimized background regimen for MDR-TB) Outcomes

for Hiv Aids Multidrug Resistant Tuberculosis Without Extensive Drug Resistance

Efficacy Outcomes
Overall Effectiveness
+70%
Response Rate
+70%
Remission Rate
+70%
Common Side Effects
Skin discoloration (reddish-brown to black)
+80%
Ichthyosis/dry skin
+40%
Nausea, abdominal pain, diarrhea
+20%
QT prolongation
+3%

WARNING: LIMITED TRIALS AVAILABLE

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Active Clinical Trials
No active trials currently recruiting for this treatment

No active trials found in ClinicalTrials.gov