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Phase 3 N=100 Randomized Treatment

A Safety and Efficacy Study of Oral Tapentadol Extended-Release in Japanese Participants

Neoplasms

Enrolled (actual)
100
Serious AEs
32.0%
Results posted
Mar 2013
Primary outcome: Primary: Percentage of Participants Who Achieved Pain Control — 84.0; 98.0 Percentage of Participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Tapentadol ER (Drug); Morphine SR (Drug)
Age
Adult, Older Adult · 20+ yrs
Sex
All
Sponsor
Janssen Pharmaceutical K.K.
Primary completion
Jan 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants Who Achieved Pain Control
84.0; 98.0
SECONDARY
Change From Baseline in Numerical Rating Scale (NRS) at Week 1, 2, 3, 4, 5, 6, 7 and 8
0.4; -0.2; 0.3; -0.3; 0.1; -0.1
SECONDARY
Number of Participants Who Discontinued Study Treatment Due to Lack of Efficacy
3; 1
SECONDARY
Number of Participants With Patient Global Impression of Change (PGIC)
1; 2; 1; 4; 11; 7
SECONDARY
Total Number of Days of Rescue Medication Over Time
15.9; 9.2
SECONDARY
Number of Doses of Rescue Medication Over Time
0.7; 0.4
SECONDARY
Average Change From Baseline in Amount of Rescue Medication Over Time
3.02; -0.15

Summary

The purpose of this study is to evaluate the conversion rate based on the number of participants achieving pain control and safety within 1 week after switching the opioid (morphine-like medications) analgesics (drug used to control pain), when tapentadol extended-release (ER) (JNS024ER) is orally administered to participants treated with around-the-clock opioid analgesics, for their moderate to severe (very serious, life threatening) chronic (lasting a long time) malignant (cancerous) tumor-related (a mass in a specific area) cancer (abnormal tissue that grows and spreads in the body) pain.

Eligibility Criteria

Inclusion Criteria

  • Participants with documented clinical diagnosis (determination of the cause of a medical problem) of any type of cancer (abnormal tissue that grows and spreads in the body)
  • Participants with mean 24-hour Numerical Rating Scale (NRS) score (11-point NRS used to measure the pain level for the past 24-hours where 0=no pain to 10=pain as bad as you can imagine) during 3 days (Day -4 to Day -2) before randomization (study drug assigned by chance) less than 4.0
  • Women must be post-menopausal, surgically sterile, or before entry and throughout the study practicing an effective method of birth control
  • Participants using immediate-release (IR) morphine hydrochloride (HCl) or oxycodone HCl hydrate as rescue medication (rescue medications are medicines that may be administered to the participants when the efficacy of the study drug is not satisfactory, or the effect of the study drug is too great and is likely to cause a hazard to the participant, or to manage an emergency situation) for breakthrough pain
  • Participants treated with around-the-clock opioid (morphine-like medications) therapy for moderate to severe (very serious, life threatening) chronic (lasting a long time), malignant (cancerous) tumor-related (a mass in a specific area) cancer (abnormal tissue that grows and spreads in the body) pain using one of the following opioid analgesics (drug used to control pain) before randomization: morphine SR tablet less than or equal to 120 milligram (mg) per day, oxycodone hydrochloride controlled release (CR) tablet: 15 mg to 80 mg per day, durotep MT (fentanyl transdermal [through the skin] matrix) patch less than or equal to 8.4 mg per patch, fentos tape less than or equal to 4 mg per tape, or oneduro patch less than or equal to 3.4 mg per patch

Exclusion Criteria

  • Participants with complicated uncontrolled/clinically significant arrhythmia (uneven heart beat)
  • Participants who had received rescue doses 3 times or more daily within 3 days (Day -4 to Day -2) before the randomization
  • History of surgery intended for the cure of the primary disease or for the treatment of cancer pain within 28 days before screening
  • Participants who had application of radiotherapy (treatment of cancer using x-rays), nerve block, or stimulation analgesia within 7 days before screening
  • Participants with known allergies (over sensitivity to a substance), hypersensitivity, or intolerance to opioid analgesics or its excipients
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01309386). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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