StAT-TB (Statin Adjunctive Therapy for TB): A Phase 2b Dose-finding Study of Pravastatin in Adults With Tuberculosis

Tuberculosis Clinical Trial

Official title:

StAT-TB (Statin Adjunctive Therapy for TB): A Phase 2b Dose-finding Study of Pravastatin in Adults With Tuberculosis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03882177
• Other study ID #: StAT-TB
• Secondary ID: 38558
• Status: Completed
• Phase: Phase 2
• Start date: February 21, 2020
• Est. completion date: December 31, 2022

Study information

• Verified date: August 2023
• Source: National Institute of Allergy and Infectious Diseases (NIAID)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to assess the safety, tolerability, and pharmacokinetics of pravastatin adjunctive therapy when combined with the standard tuberculosis (TB) treatment regimen in adults with TB.

Description:

This study will assess the safety, tolerability, and pharmacokinetics of pravastatin adjunctive therapy when combined with the standard TB treatment regimen in adults with drug-sensitive TB. The pharmacokinetic data for pravastatin will be used to choose a dose to be studied as adjunctive TB treatment in subsequent trials.

This study is a dose-escalation trial, and participants will be sequentially enrolled into four study arms. Participants will receive standard anti-TB therapy (Rifafour) and pravastatin daily for 14 days. Pravastatin will be given alone on Day 1, and pravastatin + Rifafour will be given on Days 2-15.

Total study duration for participants will be 30 days, during which time participants will attend several study visits. Study visits may include sputum specimen collection, blood and urine collection, lung function testing, and pharmacokinetic assessments. All study participants will be referred appropriately to continue standard TB treatment at study completion.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: December 31, 2022
• Est. primary completion date: May 12, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 18 years of age or older

• Clinical signs and symptoms of pulmonary tuberculosis

• Abnormal chest radiograph consistent with pulmonary tuberculosis

• At least one sputum positive for M. tuberculosis by Xpert MTB/RIF with a cycle threshold (Ct) less than 28.

• Documentation of HIV status

• Weight greater than or equal to 45 kg

• Karnofsky score of at least 60

• Ability to provide informed consent

• Ability to adhere to study follow-up visits

• Negative pregnancy test in women of child-bearing age

• Ability to adhere to contraceptive requirements and willing to use two forms of contraception: 1) a double barrier method to prevent pregnancy (i.e. use of a condom with either diaphragm or cervical cap) or 2) use of an intrauterine device in combination with a barrier contraceptive. The participant must be willing to continue these contraceptive measures throughout the duration of the study and until one week after the last dose of study medication or one week after discontinuation from study medication in case of premature discontinuation.

• Five days or fewer of anti-tuberculosis treatment within the previous 3 months

Exclusion Criteria:

• A history of severe adverse reactions to any statin or any other study agent or contraindications to use of statins.

• Current use of statins or other lipid-lower agents;

• Clinical indication for statin therapy based on cardiovascular risk:

• Familial hypercholesterolemia

• Previous history of myocardial infarction or stroke

• For HIV-positive individuals, a CD4+ T-cell count less than 350/mm^3

• Use of antiretroviral drugs

• Hemoglobin concentration less than 8 g/dL;

• Baseline creatinine kinase elevation more than three times the upper limit of normal

• Abnormal baseline laboratory values

• Baseline alanine aminotransferase (ALT) concentration more than 2.5 times the upper limit of normal (Grade 1)

• Serum creatinine concentration more than twice the upper limit of normal;

• Serum total bilirubin level greater than twice the upper limit of normal

• Platelet count less than 100,000/mm^3

• Absolute neutrophil count (ANC) less than 1,000/mm^3

• Pregnant or breastfeeding;

• Silico-tuberculosis.

• Currently receiving TB treatment

• Serologies or PCR positive for viral hepatitis (Hepatitis, B, C)

• Concomitant disorders or conditions for which isoniazid, rifampin, pyrazinamide, or ethambutol is contraindicated. These include cirrhosis, acute liver disease of any cause, acute uncontrolled gouty arthritis and peripheral neuropathy.

• Any medical or psychological condition which, in the view of the study investigator, makes study participation inadvisable.

• Infection with an isolate determined to be resistant to rifampin by GeneXpert.

• More than five days of anti-tuberculosis treatment within the previous 3 months

• Planned or current use of cyclosporine, tacrolimus, erythromycin or colchicine

• Central nervous system (CNS) TB

• Extra-pulmonary TB only, not in combination with pulmonary TB

• History of TB

Related Conditions & MeSH terms

• Pulmonary Tuberculosis
• Tuberculosis
• Tuberculosis, Pulmonary

Intervention

Drug:
• Pravastatin
Tablets, administered orally
• Rifafour
Fixed-dose combination (isoniazid, rifampin, pyrazinamide, and ethambutol) tablets, administered orally

Dietary Supplement:
• Vitamin B6
Administered orally.

Locations

Country	Name	City	State
South Africa	PHRU Non-Network CRS	Johannesburg	Gauteng

Sponsors (1)

Lead Sponsor	Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)

Country where clinical trial is conducted

South Africa, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Frequency of Grade 3 or Higher Adverse Events	Graded using the DAIDS table for Grading the Severity of Adult and Pediatric Adverse Events, Corrected Version 2.1, July 2017	Measured through Day 30
Secondary	Number of Participants Who Permanently Discontinue Assigned Study Regimen for Any Reason	(Other than new recognition of participant ineligibility based on absence of M. tuberculosis growth in baseline sputum cultures, or growth of M. tuberculosis resistant to rifampin by GeneXpert)	Measured through Day 14