Safety, Tolerability, Extended Early Bactericidal Activity and PK of Higher Doses Rifampicin in Adults With Pulmonary TB

NCT01392911 | Completed Phase 2 DMC

• 2 other identifiers: PanACEA - RUNMC - HR12007.23011.01
• Study Type: interventional
• Target: 128
• Locations: 1 country
• Sites: 2

Brief Summary

This is the first trial in a series of clinical trials that aim to bring the concept of high dose rifampicin beyond phase II of clinical development. The safety, tolerability, extended early bactericidal activity (EBA) and pharmacokinetics of several doses of Rifampicin with or without standard doses of Isoniazid, Pyrazinamide and Ethambutol in adults with newly diagnosed, uncomplicated, smear positive, pulmonary TB will be assessed. The objective of this study is to find the maximum tolerable dose of Rifampicin as monotherapy and in combination with the currently available Isoniazid, Pyrazinamide and Ethambutol. The subjects will be in the study for 24-31 days. After a screening period of 9-3 days, the subjects will receive treatment with Rifampicin as single drug during 7 days (monotherapy). This treatment will be followed by treatment with 7 days of Rifampicin and Isoniazid, Pyrazinamide and Ethambutol (combination therapy), and 7-8 days treatment with standard TB medication. All subjects will be closely monitored for side effects. This monitoring will include daily interviews and physical examination, and ECG evaluation and blood and urine analyses at specific intervals. During the 7 days of monotherapy, after the second day of the combination therapy and at the end of the combination therapy, overnight sputum will be collected from the patients to investigate the potency of high dose rifampicin to reduce this number of bacilli. The Rifampicin dose will be increased step by step and group by group. The control group will receive the standard dose of 10 mg Rifampicin/kg, whereas the first treatment group will receive 20 mg/kg. The Rifampicin dose will only be further increased for a next group of patients, if this is expected to be safe. Rifampicin is widely available and not expensive. Physicians all over the world have experience with this drug and its adverse effects. Should this study be successful, the highest dose of Rifampicin that this safe and tolerable will be given to a larger group of patients. in the next study. If increasing the dose of Rifampicin proves to be safe and effective, a higher dose of Rifampicin could be implemented broadly and quickly, and it would benefit many patients worldwide.

Conditions

Pulmonary Tuberculosis (TB)

Keywords

Dose Ranging; Extended Early Bactericidal Activity; Maximum tolerable dose; Pharmacokinetics; Pulmonary Tuberculosis; Rifampicin; Rifafour; Safety; Tolerability; Max Tolerable Dose

Outcome Measures

Primary Outcomes (2)

• The incidence and severity of adverse events associated with increasing doses of rifampicin when administered as a single drug.

  7 days

• The incidence and severity of adverse events associated with increasing doses of rifampicin when combined with isoniazid, pyrazinamide and ethambutol.

  7 days

Secondary Outcomes (4)

• The Early Bactericidal Activity (EBA) expressed as the fall of colony forming units per mL of sputum per day at the intervals: Baseline to Day 2, Baseline to Day 7, Baseline to Day 14, and Day 8 to Day 14.

  Visit 2 (Day -2) (if needed also on Visit 3 (Day -1)), Visit 4 (Day 1), Visit 5 (Day 2), Visit 6 (Day 3), Visit 7 (Day 4), Visit 8 (Day 5), Visit 9 (Day 6), Visit 10 (Day 7), Visit 12 (Day 9) and Visit 17 (Day 14)

• The change in Time to Positivity (TTP) as measured in the Mycobacterium Growth Indicator Tube (Bactec MGIT960 system) at the intervals: Baseline to Day 2, Baseline to Day 7, Baseline to Day 14, and Day 8 to Day 14.

  Visit 2 (Day -2) (if needed also on Visit 3 (Day -1)), Visit 4 (Day 1), Visit 5 (Day 2), Visit 6 (Day 3), Visit 7 (Day 4), Visit 8 (Day 5), Visit 9 (Day 6), Visit 10 (Day 7), Visit 12 (Day 9) and Visit 17 (Day 14)

• The area under the plasma concentration versus time curve (AUC) of rifampicin, and if possible also the AUC of pyrazinamide, isoniazid and ethambutol after 7 days of monotherapy with rifampicin and after 7 days of combination therapy

  Day 7 and Day 14

• Pharmacodynamic endpoints for single dose rifampicin (assessed at Day 7) and or rifampicin, isoniazid, pyrazinamide and ethambutol when administered together (assessed at Day 14).

  Day 7 and Day 14

Study Arms (9)

10 mg/kg rifampicin

ACTIVE COMPARATOR

7 Days monotherapy with 10 mg/kg rifampicin followed by 7 days standard TB treatment, i.e. Rifafour® e275 once daily including the standard dose of rifampicin.

Drug: Rifampicin

20 mg/kg Rifampicin

EXPERIMENTAL

7 Days monotherapy with 20 mg/kg rifampicin followed by 7 days combination therapy consisting of 20 mg/kg rifampicin plus the standard doses of isoniazid, ethambutol and pyrazinamide.

Drug: Rifampicin

25 mg/kg Rifampicin

EXPERIMENTAL

7 Days monotherapy with 25 mg/kg rifampicin followed by 7 days combination therapy consisting of 25 mg/kg rifampicin plus the standard doses of isoniazid, ethambutol and pyrazinamide.

Drug: Rifampicin

30 mg/kg Rifampicin

EXPERIMENTAL

7 Days monotherapy with 30 mg/kg rifampicin followed by 7 days combination therapy consisting of 30 mg/kg rifampicin plus the standard doses of isoniazid, ethambutol and pyrazinamide.

Drug: Rifampicin

35 mg/kg Rifampicin

EXPERIMENTAL

7 Days monotherapy with 35 mg/kg rifampicin followed by 7 days combination therapy consisting of 35 mg/kg rifampicin plus the standard doses of isoniazid, ethambutol and pyrazinamide.

Drug: Rifampicin

40 mg/kg Rifampicin

EXPERIMENTAL

7 Days monotherapy with 40 mg/kg rifampicin followed by 7 days combination therapy consisting of 40 mg/kg rifampicin plus the standard doses of isoniazid, ethambutol and pyrazinamide.

Drug: Rifampicin

45 mg/kg Rifampicin

EXPERIMENTAL

7 Days monotherapy with 45 mg/kg rifampicin followed by 7 days combination therapy consisting of 45mg/kg rifampicin plus the standard doses of isoniazid, ethambutol and pyrazinamide.

Drug: Rifampicin

50 mg/kg rifampicin

EXPERIMENTAL

7 Days monotherapy with 50 mg/kg rifampicin followed by 7 days combination therapy consisting of 50 mg/kg rifampicin plus the standard doses of isoniazid, ethambutol and pyrazinamide.

Drug: Rifampicin

55 mg/kg Rifampicin

EXPERIMENTAL

7 Days monotherapy with 55 mg/kg rifampicin followed by 7 days combination therapy consisting of 55 mg/kg rifampicin plus the standard doses of isoniazid, ethambutol and pyrazinamide.

Drug: Rifampicin

Interventions

Rifampicin DRUG

High dose rifampicin

Also known as: Rifadin, Rifafour

10 mg/kg rifampicin; 20 mg/kg Rifampicin; 25 mg/kg Rifampicin; 30 mg/kg Rifampicin; 35 mg/kg Rifampicin; 40 mg/kg Rifampicin; 45 mg/kg Rifampicin; 50 mg/kg rifampicin; 55 mg/kg Rifampicin

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• The patient is able and willing to provide written, informed consent prior to all trial-related procedures including HIV testing.
• The patient is aged between 18 and 65 years, inclusive.
• The patient has a body weight (in light clothing and with no shoes) between 40 and 85 kg, inclusive.
• The patient is a newly diagnosed, previously untreated, uncomplicated, sputum smear-positive, pulmonary TB patient.
• The patient has a normal chest X-ray or a picture which in the opinion of the Investigator is compatible with TB.
• The patient is sputum positive on direct microscopy for acid-fast bacilli (at least 1+ on the IUATLD/WHO scale (Appendix 4)).
• The patient is able to produce an adequate volume of sputum as estimated from a spot assessment (estimated 10 ml or more overnight production).
• The patient has a negative serum pregnancy test (female subjects of childbearing potential only)
• The patient agrees to use a highly effective method of birth control (i.e. two of the following precautions: tubal ligation, vaginal diaphragm, intrauterine device, condom, oral contraceptives, contraceptive implant, combined hormonal patch, combined injectable contraceptive or depot-medroxyprogesterone acetate, partner(s) has/have had a vasectomy) throughout the participation in the trial and for 1 week after last dose, unless she and her partner(s) are sterile (that is, women who have had a bilateral oophorectomy and/or hysterectomy or have been postmenopausal for at least 12 consecutive months; men who have had bilateral orchidectomy).
• A Karnofsky score of at least 60 (requires occasional assistance but is able to care for most of his/her needs).

You may not qualify if:

• The patient is in poor general condition where any delay in treatment cannot be tolerated per discretion of the Investigator.
• Rifampicin-resistant bacteria have been detected in the patient's sputum specimen collected within the Pre-Treatment Period and tested at the study laboratory.
• The patient has received treatment with any drug active against MTB within the 3 months prior to Visit 1: isoniazid, ethambutol, amikacin, cycloserine, rifabutin, rifampicin, streptomycin, kanamycin, para-aminosalicylic acid, rifapentine, pyrazinamide, thioacetazone, capreomycin, quinolones, thioamides.
• The patient has a history of allergy to isoniazid, ethambutol, rifampicin and pyrazinamide,
• The patient has a history of previous TB.
• The patient has Hepatitis B.
• The patient had Hepatitis C.
• The patient is infected with HIV and has a CD4 count \< 350 cells/uL (Visit 1).
• The patient is receiving antiretroviral therapy (ART).
• The patient has been taking rifampicin within 30 days prior to Visit 1.
• The patient is a diabetic using insulin.
• The patient is pregnant or breast-feeding (female patients only).
• The patient has a history and/or presence (or evidence) of neuropathy or epilepsy.
• The patient has a history of or current clinically relevant cardiovascular disorder such as:
• heart failure, coronary heart disease, hypertension, arrhythmia, tachyarrhythmia or status after myocardial infarction.

Sponsors & Collaborators

• Radboud University Medical Center: lead
• European and Developing Countries Clinical Trials Partnership (EDCTP): collaborator
• Department of Clinical Pharmacy, University Medical Centre St Radboud, The Netherlands.: collaborator
• University Centre for Chronic Diseases Dekkerswald, Groesbeek, NL: collaborator

Study Sites (2)

TASK Applied Science

Bellville, 7531, South Africa

Location

University of Cape Town Lung Institute

Mowbray, 7700, South Africa

Location

Related Publications (3)

• Te Brake LHM, de Jager V, Narunsky K, Vanker N, Svensson EM, Phillips PPJ, Gillespie SH, Heinrich N, Hoelscher M, Dawson R, Diacon AH, Aarnoutse RE, Boeree MJ; PanACEA Consortium. Increased bactericidal activity but dose-limiting intolerability at 50 mg.kg-1 rifampicin. Eur Respir J. 2021 Jul 8;58(1):2000955. doi: 10.1183/13993003.00955-2020. Print 2021 Jul.

  PMID: 33542056 DERIVED

• Svensson RJ, Svensson EM, Aarnoutse RE, Diacon AH, Dawson R, Gillespie SH, Moodley M, Boeree MJ, Simonsson USH. Greater Early Bactericidal Activity at Higher Rifampicin Doses Revealed by Modeling and Clinical Trial Simulations. J Infect Dis. 2018 Aug 14;218(6):991-999. doi: 10.1093/infdis/jiy242.

  PMID: 29718390 DERIVED

• Boeree MJ, Diacon AH, Dawson R, Narunsky K, du Bois J, Venter A, Phillips PP, Gillespie SH, McHugh TD, Hoelscher M, Heinrich N, Rehal S, van Soolingen D, van Ingen J, Magis-Escurra C, Burger D, Plemper van Balen G, Aarnoutse RE; PanACEA Consortium. A dose-ranging trial to optimize the dose of rifampin in the treatment of tuberculosis. Am J Respir Crit Care Med. 2015 May 1;191(9):1058-65. doi: 10.1164/rccm.201407-1264OC.

  PMID: 25654354 DERIVED

MeSH Terms

Conditions

Tuberculosis, Pulmonary

Interventions

Rifampin

Condition Hierarchy (Ancestors)

Tuberculosis; Mycobacterium Infections; Actinomycetales Infections; Gram-Positive Bacterial Infections; Bacterial Infections; Bacterial Infections and Mycoses; Infections; Respiratory Tract Infections; Lung Diseases; Respiratory Tract Diseases

Intervention Hierarchy (Ancestors)

Rifamycins; Heterocyclic Compounds, 4 or More Rings; Heterocyclic Compounds, Fused-Ring; Heterocyclic Compounds; Lactams, Macrocyclic; Macrocyclic Compounds; Polycyclic Compounds

Study Officials

• Martin Boeree, MD, PhD

  Radboud university medical center, University Centre for Chronic Deseases Dekkerswald

  STUDY CHAIR

• Rob Aarnoutse, PharmD, PhD

  Radboud University Medical Center

  STUDY CHAIR

• Andreas Diacon, MD

  TASK Applied Science

  PRINCIPAL INVESTIGATOR

• Rodney Dawson, MD

  University of Cape Town Lung Institute

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: FACTORIAL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 14, 2011
• First Posted: July 13, 2011
• Study Start: June 1, 2011
• Primary Completion: July 1, 2018
• Study Completion: November 1, 2018
• Last Updated: November 26, 2018

Record last verified: 2018-11

Locations

ZA (2)