An Interventional Study to Compare the Efficacy and Tolerability With Targin® in Non-malignant Chronic Pain (GLORY)

Mundipharma

Status and phase

Completed

Phase 4

Conditions

Chronic Pain

Treatments

Drug: Oxycodone/naloxone

Study type

Interventional

Funder types

Industry

Identifiers

NCT01811186

OXN12-KR-403

Details and patient eligibility

About

Objectives:

Objective of main interest
- To assess the drop-out rate caused by adverse event* after 6 weeks treatment
Further objectives
- To assess the drop-out rate caused by adverse event* after 1 week treatment
- To assess the pain reduction rate after 6 weeks treatment from baseline
- To assess the Euroquol (EQ-5D) quality of life
- To assess physician's overall satisfaction
- To assess subject's overall satisfaction
- To assess safety

Full description

Study Design (Methodology):

This will be a single center, open-label, randomised, phase IV, exploratory interventional study to compare the efficacy and tolerability of current titration patterns and slow titration pattern with Targin® (Oxycodone/Naloxone) in the treatment of moderate to severe non-malignant chronic pain patients who are dissatisfied with their current analgesic medication World Health Organisation (WHO) step II analgesics).

Upon providing written informed consent, subject will be screened in the study and assessment will be performed at that time such as safety laboratory assessments, physical examination, vital sign, medical history taking, 24 hours pain intensity score. If the patient is eligible in inclusion/exclusion criteria at the time of visit 1, the patient will be randomized in a 1:1 ratio to allocate in Group A or Group B. Re-screening, study drug dose interruption is not allowed.

Enrollment

261 patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or female ≥ 20 and <80 years of age
Patients who have non-malignant chronic pain(≥90 days)
Patients who have moderate to severe pain intensity which is not controlled with non-strong opioid
Naïve patients for Oxycodone/Naloxone (Naïve patient defined as who did not treated for 90 days)
Naïve patients for strong opioid (Naïve patient defined as who did not treated for 90 days)
Patients who signed a written informed consent form

Exclusion criteria

Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant.
Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive urine pregnancy test
Patients with known hypersensitivity to Oxycodone/Naloxone or to any of the excipients
Patient who needs acute dose titration or whose pain intensity fluctuate significantly in a short period according to investigator's judgment
Having used other investigational drugs at the time of enrollment, or within 30 days of enrollment