The Safety of Tuberculosis Treatments by Oral Inhalation

Healthy Clinical Trial

Official title:

Clinical Trial Phase I of Antituberculosis Dry Powder Aerosols

Clinical Trial Details — Status: Unknown status

Administrative data

• NCT number: NCT01785927
• Other study ID #: RES.no. 18/2554
• Status: Unknown status
• Phase: Phase 1
• First received: February 5, 2013
• Last updated: February 5, 2013
• Start date: February 2013
• Est. completion date: April 2013

Study information

• Verified date: February 2013
• Source: Prince of Songkla University
• Contact: Teerapol Srichana, PhD
• Phone: 66-74-288979
• Email: teerapol.s[@]psu.ac.th
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The inhaled route of delivery has always been associated with the considerable challenge of getting the drug to its target. The lungs are a highly complex organ designed to filter inspired air, with many different cell types contributing to their function. Furthermore, the lungs may change dramatically when afflicted by disease resulting in an internal environment that works against the drug reaching and interacting successfully with the target. For targets in the upper airways this will have lesser significance, but drug delivery to the deep lung may be impeded by changes such as mucus hyper-secretion or thickening or airway narrowing.

In order to interpret toxicology findings it is necessary to reconcile test sensitivity, background biological variation, normal responses to inhaled materials and drug or medicine-specific adverse effects. Identification of adverse end-points is an area where better control data sets might help discern true adverse effects from a normal physiological lung response. The lung responds acutely to inhalation of irritant materials by hyper-secretion of mucus, chemokine release, inflammatory cell recruitment and cough and collectively these may be characterized as non-specific irritancy.

Description:

Four formulations of antituberculosis drug (rifampicin, isoniazid, pyrazinamide, and levofloxacin) will be administered to each patient by randomization. Each formulation will be assigned the code, such as A, B, C, or D, and the treatment sequences will be generated as ABCD (sequence 1), BCDA (sequence 2), CDAB (sequence 3) and DABC (sequence 4). On the first day of drug dosing in period I, volunteers will be randomly assigned to a sequence of treatments as indicated in a pre-printed randomization scheme, which was generated using block randomization with block sizes of 4 and 6, and the allocation ratio of 1:1. Subjects will be stratified by sex. Subjects in sequence 1 will receive treatment A during the first study period and will then cross over to receive treatment B, C, and D at the second, third and fourth periods, respectively (each after a 7-day washout period).

Recruitment information / eligibility

• Status: Unknown status
• Enrollment: 40
• Est. completion date: April 2013
• Est. primary completion date: April 2013
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• Aged 18-45 years

• Body mass index 18-27 kg/m2

• Healthy

• In the case of reproductive age woman, effective contraceptive will be used for at least 4 weeks prior to a screening examination until the end of study.

• Non-lactating women

• Patients who are willing to participate in the trial and will first sign the informed consent form.

Exclusion Criteria:

• Allergic to any antituberculosis drugs or other components

• High blood pressure (diastolic pressure > 90 mmHg)

• Liver enzymes (AST and ALT) > 2 times of upper normal value

• Pregnancy or lactation

• No underlying diseases such as asthma, COPD, chronic kidney disease, diabetes mellitus, liver disease, immunocompromised deficiency, etc.

• HBsAg positive

• Abnormality in chest X-ray or routine laboratory tests

• Smokers > 10 cigarette/day or smokers < 10 cigarettes/day who could not quit at least 7 days before study and throughout study (including the washout between periods)

• Regular alcohol consumption (more than 1 time/week) or alcohol consumption within 7 days prior to the study

Related Conditions & MeSH terms

• Healthy

Intervention

Other:
• ABCD
Rifampicin, isoniazid, pyrazinamide, and levofloxacin dry powders will be administered to each patient by randomization. Each formulation will be assigned the code, such as A, B, C, or D, and the treatment sequences will be generated as ABCD (sequence 1), BCDA (sequence 2), CDAB (sequence 3) and DABC (sequence 4). On the first day of drug dosing in period I, volunteers will be randomly assigned to a sequence of treatments as indicated in a pre-printed randomization scheme, which was generated using block randomization with block sizes of 4 and 6, and the allocation ratio of 1:1. Subjects will be stratified by sex. Subjects in sequence 1 will receive treatment A during the first study period and will then cross over to receive treatment B, C, and D at the second, third and fourth periods, respectively (each after a 7-day washout period).

Locations

Country	Name	City	State
Thailand	Songklanagarind Hospital	Hat Yai	Songkla

Sponsors (2)

Lead Sponsor	Collaborator
Prince of Songkla University	National Research Council of Thailand

Country where clinical trial is conducted

Thailand, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Adverse events		Two months
Primary	Cytokine levels (Tumor Necrosis Factor-a and Interleukin-1ß)		Two months
Secondary	Liver function tests (tB/dB, AST, ALT, ALP)		Two months