E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
Subjects with inadequately controlled, moderate to severe, chronic, cancer-related pain |
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MedDRA Classification |
E.1.2 Medical condition or disease under investigation |
E.1.2 | Version | 9.1 |
E.1.2 | Level | LLT |
E.1.2 | Classification code | 10058019 |
E.1.2 | Term | Cancer pain |
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E.1.3 | Condition being studied is a rare disease | No |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
The primary objective of this study is to evaluate the analgesic efficacy, safety, and tolerability of a single SC dose (9 mg in 0.3 mL) of JNJ-42160443 compared with placebo as adjunctive therapy to standard pain therapy in subjects with inadequately controlled, moderate to severe, chronic, cancer-related pain. The primary efficacy objective of this study is to evaluate the analgesic effect of JNJ-42160443 compared with placebo, as measured by the change from baseline to the end of the double-blind treatment phase in the average cancer-related pain intensity score, using an 11-point numerical rating scale (NRS), with 0=no pain and 10=pain as bad as you can imagine.
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E.2.2 | Secondary objectives of the trial |
The secondary objectives of this study are to evaluate the efficacy of JNJ-42160443 compared with placebo, as measured by the Brief Pain Inventory (BPI) Short Form, Patient and Clinical Global Impression of Change (PGIC and CGIC), and baseline and breakthrough opioid use and to evaluate the immunogenicity (antibodies to JNJ-42160443) associated with JNJ-42160443 treatment.
The pharmacokinetics of JNJ-42160443 after SC doses will also be examined.
Exploratory Objectives The exploratory objectives of this study are to investigate the effects of improvements in pain relief with JNJ-42160443 on the severity of fatigue, aspects of daily activities, and anxiety/depression.
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E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
· Have a life expectancy of at least 4 months · Have a diagnosis of moderate to severe pain directly related to an active cancer and inadequately controlled by standard pain therapies; the primary site of pain should not be pain due to treatment of the cancer (eg, post-operative or procedural pain, chemotherapy- or radiotherapy-induced pain, or pain due to other comorbidities related to the cancer (eg, chronic postherpetic neuralgia, chemotherapy-induced neuropathy, osteoporotic fractures) · Currently receiving opioid analgesics at screening: – The baseline, around-the-clock dose should be ³60 mg of oral morphine equivalents, not including breakthrough pain medication doses – The baseline opioid dose should be given as a sustained-release formulation at a stable dose for at least 1 week before screening – A stable, baseline opioid dose is defined as a dose that does not fluctuate by more than 50% from the average dose over the 1 week before screening; the dose may fluctuate by more than 50% for up to 2 days, if medically necessary – The baseline opioid dose is expected to remain stable during the double-blind treatment phase – Not more than an average of 4 breakthrough pain medication doses per day during the 1 week before screening · If currently receiving nonopioid analgesics and adjuvant pain therapies (eg, anticonvulsants, antidepressants, NSAIDs, corticosteroids, pharmaceutical cannabinoids [eg, MarinolÒ, SativexÒ, CesametÔ]), must be at stable doses for 2 weeks before screening and expected to remain stable during the double-blind treatment phase · Have an average daily pain intensity score of ³5 averaged over the last 3 days before randomization (Day 1) using an 11-point NRS, with 0=no pain and 10=pain as bad as you can imagine
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E.4 | Principal exclusion criteria |
· History of bone marrow transplant (BMT) within the past 10 years. If a subject had BMT >10 years ago, must not have had a history of graft versus host disease and not currently receiving immunosuppressive therapy. · History of leukemia · History of small cell lung cancer · History of neuroendocrine tumors · History of any of the following: – Seizure disorders within the past year – Multiple sclerosis within the past year – Intrathecal therapy, Ommaya reservoirs, and ventricular shunts within the past year – Radiotherapy to the cerebral area within the past year – Mild or moderate traumatic brain injury within the past year – Stroke within the past year – Transient ischemic attack within the past year – Severe traumatic brain injury within the past 15 years (consisting of ³ 1 of the following: brain contusion, intracranial hematoma, either unconsciousness or posttraumatic amnesia lasting more than 24 hours) or with residual sequelae suggesting transient changes in consciousness – Any other condition suggesting compromised blood brain barrier (contact the sponsor’s medical officer to discuss if unclear) · Presence of cerebral metastases (Note: Diagnostic testing will not be required for ruling out cerebral metastases.) · Any other condition suggesting compromised blood brain barrier (contact the sponsor’s medical officer to discuss if unclear) · Presence of disseminated or severe organ-related herpes virus disease (eg, cytomegalovirus retinitis or cytomegalovirus nephritis) · Presence of severe chronic obstructive pulmonary disease (COPD), according to American Thoracic Society (ATS)/European Respiratory Society (ERS) Standards for the Diagnosis and Management of Patients with COPD · Oxygen saturation (pO2) <90% on room air or £2 L/min of oxygen therapy for subjects who have clinically significant compromised lung function · Planned initiation of new chemotherapy regimen or radiotherapy, bisphosphonates, or hormonal or growth factor therapy during the double-blind treatment phase · Planned major surgical procedure during the double-blind treatment phase · Currently using patient-controlled analgesia or IV opioids as chronic baseline pain therapy · Currently receiving ³60 mg-equivalents of prednisone per day To be eligible to enter the open-label extension phase, the following key criterion must be met: · Must have completed the double-blind treatment phase of the study
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E.5 End points |
E.5.1 | Primary end point(s) |
The primary efficacy evaluation is the average cancer-related pain intensity in the last 24 hours using an 11-point NRS, with 0=no pain and 10=pain as bad as you can imagine. The primary efficacy endpoint is the change from baseline to the end of the double-blind treatment phase in the average cancer-related pain intensity score, averaged over the last 3 days before randomization and over the last 7 days of the double-blind treatment phase.
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E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | No |
E.6.2 | Prophylaxis | No |
E.6.3 | Therapy | No |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | Yes |
E.6.7 | Pharmacodynamic | No |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | No |
E.6.11 | Pharmacogenomic | Yes |
E.6.12 | Pharmacoeconomic | No |
E.6.13 | Others | No |
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | No |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | No |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | Yes |
E.7.3 | Therapeutic confirmatory (Phase III) | No |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | Yes |
E.8.1.1 | Randomised | Yes |
E.8.1.2 | Open | No |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | Yes |
E.8.1.5 | Parallel group | No |
E.8.1.6 | Cross over | Yes |
E.8.1.7 | Other | No |
E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | No |
E.8.2.2 | Placebo | Yes |
E.8.2.3 | Other | No |
E.8.3 |
The trial involves single site in the Member State concerned
| No |
E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
E.8.4.1 | Number of sites anticipated in Member State concerned | 5 |
E.8.5 | The trial involves multiple Member States | Yes |
E.8.5.1 | Number of sites anticipated in the EEA | 20 |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
E.8.6.2 | Trial being conducted completely outside of the EEA | Information not present in EudraCT |
E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
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E.8.7 | Trial has a data monitoring committee | Yes |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
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E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 2 |
E.8.9.1 | In the Member State concerned months | 5 |
E.8.9.1 | In the Member State concerned days | 7 |
E.8.9.2 | In all countries concerned by the trial years | 2 |
E.8.9.2 | In all countries concerned by the trial months | 5 |
E.8.9.2 | In all countries concerned by the trial days | 7 |