Safety and Pharmacokinetics (PK) in Multidrug-Resistant (MDR) Refractive Tuberculosis

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Otsuka Pharmaceutical Development & Commercialization, Inc.
ClinicalTrials.gov Identifier:
NCT01131351
First received: May 25, 2010
Last updated: June 26, 2012
Last verified: June 2012

May 25, 2010
June 26, 2012
February 2010
May 2011   (final data collection date for primary outcome measure)
  • Vital signs [ Time Frame: 9 months ] [ Designated as safety issue: Yes ]
    blood pressure, heart rate, respiratory rate, body temperature and body weight
  • Clinical Laboratory Assessments [ Time Frame: 9 months ] [ Designated as safety issue: Yes ]
    Hematology, chemistry, and urinalysis
  • Standard 12-lead ECG [ Time Frame: 9 months ] [ Designated as safety issue: Yes ]
  • Reported Adverse Events [ Time Frame: 9 months ] [ Designated as safety issue: Yes ]
  • PK assessments [ Time Frame: 12 months ] [ Designated as safety issue: No ]
    Pharmacokinetics parameters including maximum observed plasma concentration (Cmax), time to maximum plasma concentration (tmax), lowest plasma concentration during the 24 hours postdose (Cmin), and area under the plasma concentration-time curve from time 0 to 24 hours (AUC0-24h) at various time points.
Same as current
Complete list of historical versions of study NCT01131351 on ClinicalTrials.gov Archive Site
Sputum Culture Conversion [ Time Frame: 24 weeks ] [ Designated as safety issue: No ]
Efficacy evaluation of sputum culture conversion including proportion of patients with sputum culture conversion at Day 168 evaluated with MGIT® culture system and solid media
Same as current
Not Provided
Not Provided
 
Safety and Pharmacokinetics (PK) in Multidrug-Resistant (MDR) Refractive Tuberculosis
A Phase 2, Multi-center, Non-controlled, Open-label Dose Escalation Trial to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of Orally Administered OPC-67683 Two Times Daily to Patients With Pulmonary Multidrug-Resistant Tuberculosis Refractory to Conventional Treatment

The purpose of this study is:

  • To evaluate the safety and tolerability of orally administered OPC-67683 when administered two times daily (BID) to MDR TB patients refractory to treatment with an optimized background regimen of anti-TB medications (OBR).
  • To evaluate the pharmacokinetics (PK) of OPC-67683 and metabolites.
Not Provided
Interventional
Phase 2
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Tuberculosis
Drug: OPC-67683
Dosage-500-800 mg Strength 250-400 mg Frequency b.i.d.
Experimental: OPC-67683
Dose Escalation
Intervention: Drug: OPC-67683
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
10
May 2011
May 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Provide written, informed consent prior to all trial-related procedures
  2. Male or female patients aged between 18 and 64 years, inclusive.
  3. Able to produce sputum for mycobacterium culture or able to obtain sputum produced through Induction.
  4. At least three sputum mycobacterium cultures positive for MTB with in-vitro resistance to isoniazid and rifampicin during the previous 270 days (9 months) despite treatment with first and second line anti-TB drugs, including one positive culture within the previous 60 days from the time of sputum collection, prior to date of screening initiation (defined as the date the ICF is signed and screening begins).
  5. Sputum mycobacterial culture positive for MTB with in-vitro susceptibility to at least one anti-TB Medication within the previous 60 days prior to the date of screening initiation.
  6. Patient judged by the investigator to have potential for clinical benefit from OPC-67683 exposure.
  7. Female patients of childbearing potential must have a negative urine pregnancy test and agree to use a highly effective method of birth control (for example, two of the following precautions: tubal ligation, vaginal diaphragm, intrauterine device, oral contraceptives, contraceptive implant,combined hormonal patch, combined injectable contraceptive or depot-medroxyprogesterone acetate) throughout the participation in the trial and for 22 weeks after last dose (to cover duration of ovulation).
  8. Male patients must agree to use an adequate method of contraception (double barrier) throughout the participation in the trial and for 30 weeks after last dose (to cover duration of spermatogenesis.

Exclusion Criteria:

  1. A history of allergy to any nitro-imidazoles or nitro-imidazole derivatives at any time.
  2. Use of the medications in Section 4.1 including: use of amiodarone at any time during the previous 12 months, use of other anti-arrhythmics for the previous 30 days, as well as use of certain antidepressants, Anti-histamines, any macrolides, for the previous 14 days.
  3. Any current serious concomitant conditions or renal impairment characterized by serum creatinine levels ≥265 μmol/L or hepatic impairment characterized by ALT and/or aspartate transferase (AST)levels 3 times the upper limit of the laboratory reference range.
  4. Current clinically relevant changes in the Screening ECG such as any atrioventricular (AV) block, prolongation of the QRS complex over 120 msec (in both male and female patients), or of the QTcF interval over 450 msec in male patients and over 470 msec in female patients.
  5. Current clinically relevant cardiovascular disorder such as heart failure, coronary heart disease,uncontrolled or poorly controlled hypertension, arrhythmia, tachyarrhythmia or status after myocardial infarction.
  6. For patients with HIV infection, CD4 cell count < 350/mm3 or on treatment with anti-retroviral medication for HIV infection.
  7. Karnofsky score < 50%.
  8. Any current diseases or conditions in which the use of nitro-imidazoles or nitro-imidazole derivates is contra-indicated.
Both
18 Years to 64 Years
No
Contact information is only displayed when the study is recruiting subjects
Lithuania,   Latvia
 
NCT01131351
242-08-210
Yes
Otsuka Pharmaceutical Development & Commercialization, Inc.
Otsuka Pharmaceutical Development & Commercialization, Inc.
Not Provided
Not Provided
Otsuka Pharmaceutical Development & Commercialization, Inc.
June 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP