Pulmonary Tuberculosis
Conditions
Keywords
HUEXC030, Pulmonary Tuberculosis
Brief summary
Assess the Efficacy of HUEXC030 as Add-on Excipient to Eradicate Anti-Tuberculosis Drugs Induced Hepatic Injury ( ATDH ) in Subjects with Pulmonary Tuberculosis
Detailed description
The study drug is Isoniazid formulated with HUEXC030 as excipient for eradicating ATDH, whereas the reference control is Isoniazid formulated with inactive excipient. Subjects who fulfill all the entry criteria and have written informed consent will be enrolled to the study. Eligible subjects will be randomized in a 1:1 ratio to receive study drug or reference control drug. Subjects will be genotyped according to a selected panel of single nucleotide polymorphisms (SNPs) and categorized into high risk or low risk groups for occurring ATDH via a specific haplotype consists of CYP2E1 and NAT2 SNPs. Based on an extensive study result during 2007 to 2011,the estimated frequency for patients bearing high risk genotypes in Taiwanese population is around 25%. Approximately 352 subjects will be enrolled for genotype screening in order to recruit 88 high risk subjects for each of 44 subjects in the intervention and control arms. Subjects who are stratified as high risk groups will be administered the test drug or reference control drugs oral daily for 6 months or until treatment completion, i.e. bacteriologically confirmed negative of active M. tuberculosis. Subjects who are of low risk genotype will be removed from study after 8 weeks of study treatment, then return to conventional TB medication under the care of their investigator for at least one follow-up visit at 4 weeks after the End of Study.
Interventions
DRUGIsoniazid with HUEXC030 and RZE
Subjects will receive oral study drug daily in accordance with the following regimen, that is, INH, RMP, PZA, and EMB for the first 2 months followed by INH, RMP and EMB (if medically indicated) daily for 4 additional months
DRUGHRZE
the same as experimental group,without the excipient of HUEXC030 only
Sponsors
National Defense Medical Center, Taiwan
National Research Program for Biopharmaceuticals, Taiwan
Orient Pharma Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Main inclusion criteria: 1. A definite case of pulmonary TB 2. Patient who is exposed to 3 or less doses of first-line anti-TB drug treatment for current disease. 3. Age ≥ 20 years 4. Have well documented baseline liver function tests that indicates patient's adequate liver function for enrollment to study. i. AST and ALT \< 3x ULN ii. total serum bilirubin \< 2.0 mg/dL Main
Exclusion criteria
1. Have alcoholic liver disease or habitual alcohol consumption \> 30 g/day for more than one year 2. Previously diagnosed of: i. extra-pulmonary TB without concomitant lung invasion ii. HIV iii. liver malignancy iv. liver cirrhosis v. any other systemic diseases that may cause liver dysfunction 3. Documented history of serious allergic reaction or resistance to isoniazid, rifampicin, ethambutol, pyrazinamide, sugar alcohols or any structurally related compounds 4. Subjects who will be using the following therapies after TB treatment starts: i. antiretroviral agents ii. oral corticosteroids 5. Subjects are pregnant or lactating 6. Subjects with child-bearing potential who are not committed to take reliable contraception during the participation of the study and at least 4 weeks after the end of the study treatment 7. Subjects with any other serious disease considered by the investigator not in the condition to enter into the trial
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| ALT change from baseline to the 8 weeks of study treatment | 8 weeks | The primary efficacy endpoint is the time-interval weighted area under the curve (AUC) of change from baseline in serum ALT, primarily in patients with high risk genotypes. The area under ALT change curve was estimated using the linear trapezoidal rule. The AUC was a measure of cumulative ALT differences from baseline to the 8 weeks of double-blind treatment period. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of ATDH in high risk genotype subjects treated with investigational drugs | 8 weeks | Primarily in patients with high risk genotypes, the lowering incidence of ATDH in subjects treated with anti-TB drugs in combination with HUEXC030 for 8 weeks. |
| Percentage of patients cured by the end of treatment | 8 weeks | At 8 weeks, the investigational product is not inferior in effectiveness of TB treatment to the control drug, primarily in patients with high risk genotypes. |
| The overall reduced incidence of ATDH in subjects treated with investigational drugs | 26 weeks | Compared to control drugs, the overall reduced incidence of ATDH in all enrolled subjects treated with investigational drugs at study ends. |
| The lowering average level of liver function tests | 26 weeks | Compared to control drugs, the lowering average level of liver function tests in all enrolled subjects treated with investigational drugs at study ends. |
Countries
Taiwan
Outcome results
None listed