Phase 2
N=182
Study to Evaluate MK-6096 in the Treatment of Painful Diabetic Neuropathy (PDN) in Adults (MK-6096-021)
Diabetic Neuropathy, Painful
Bottom Line
View on ClinicalTrials.gov: NCT01564459 ↗Enrolled (actual)
182
Serious AEs
1.1%
Results posted
Aug 2016
Primary outcome: Primary: Time to Efficacy Failure (TTEF) - Primary Responders — NA; NA Days
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- MK-6096 (Drug); Placebo (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Merck Sharp & Dohme LLC
- Primary completion
- Apr 2013
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Time to Efficacy Failure (TTEF) - Primary Responders |
NA; NA | — |
| PRIMARY Percentage of Participants Who Experienced 1 or More Adverse Events (AE) |
24.7; 23.9; 13.4 | — |
| PRIMARY Percentage of Participants Who Were Discontinued Form the Study Due to an AE |
3.8; 0.0; 1.2 | — |
| SECONDARY TTEF - All Responders |
NA; NA | — |
| SECONDARY Change in Pain Intensity Scores - Primary Responders |
-0.104; 0.482 | 0.269 |
| SECONDARY Change in Pain Intensity Scores - All Responders |
-0.318; 0.368 | 0.108 |
Summary
The purpose of this study is to evaluate the safety and effectiveness of MK-6096 in the treatment of painful diabetic neuropathy (PDN) in adults.
Eligibility Criteria
Inclusion Criteria
- Has a primary diagnosis of painful diabetic neuropathy (PDN) for at least 6 months.
- Is able to understand & use an electronic diary to complete daily questionnaires.
- If female of reproductive potential, agrees to use acceptable contraception from Screening through to at least 2 weeks after last dose of study drug.
- Is on a stable dose of antihyperglycemic treatment for at least 1 month, with hemoglobin A1C level of no more than 11%.
- If taking an allowable around-the-clock medication for chronic pain, has been on a stable dose for at least 1 month & agrees to stay on same dose during the study.
- Agrees to not start therapy with opioids, pregabalin, gabapentin, duloxetine or any other medications used to treat neuropathic pain during the study.
- Has a regular bedtime of before 1 AM (01:00).
- Agrees to limit alcohol consumption to no more than 3 drinks a day, with no drinks within 3 hours before bedtime. One drink is defined as: 1) 12 ounces of beer; 2) 4 ounces of wine; or 3) 1 ounce of liquor (80 proof or 40% alcohol).
- Agrees to limit caffeine consumption to no more than 5 standard 6-oz. cups of caffeinated beverages or no more than 600 mg caffeine a day, with no caffeinated beverages after 4 PM (16:00).
- Agrees to maintain a relatively consistent level of activity throughout the study.
Exclusion Criteria
- Is pregnant or breastfeeding, or expects to become pregnant during the study.
- Expects to donate eggs or sperm during the study or within 90 days after last dose of study drug.
- Has had ineffective treatment with more than 3 neuropathic pain drugs.
- Anticipates need for surgery during the study.
- Has another existing type of pain that is as severe as or greater than the pain under study OR is not able to distinguish the pain under study from another existing pain condition.
- Has post herpetic neuralgia (PHN); small fiber predominant neuropathy (SFN); idiopathic sensory neuropathy (ISN); complex regional pain syndrome; sensory neuropathies; or pain caused by radiation/chemotherapy/amputation/human immunodeficiency virus (HIV) infection.
- Has received a nerve block for pain within past 6 weeks.
- Has a history of pernicious anemia, untreated hypothyroidism, or amputations other than toes.
- Has a history of narcolepsy, cataplexy, circadian rhythm disorder, parasomnia, sleep-related breathing disorder, restless legs syndrome, periodic limb movement disorder, excessive daytime sleepiness, or difficulty sleeping due to a medical condition (i.e. asthma, Gastroesophageal Reflux Disease (GERD)) other than PDN.
- Has any history of a neurological disorder, including: seizure disorder, stroke, transient ischemic attack, multiple sclerosis, cognitive impairment, or significant head trauma with sustained loss of consciousness.
- Has a current evidence or history within past 6 months of unstable cardiovascular disorder, including: acute coronary syndrome; unstable angina; congestive heart failure; cardiogenic syncope; cardiomyopathy; or symptomatic arrhythmia.
- Has a Body Mass Index (BMI) of more than 40 kg/m^2.
- Has any of the following: 1) evidence of ongoing depression or suicidality; 2) a lifetime history of bipolar disorder, a psychotic disorder, or posttraumatic stress disorder; 3) a psychiatric condition requiring treatment with a prohibited medication; or 3) other current psychiatric condition that might interfere with ability to participate in the study.
- Is at imminent risk of self-harm or harm to others.
- Has a history of substance abuse or dependence. Substances include alcohol, marijuana, hypnotics, other prescription drugs, & drugs of abuse, but exclude nicotine.
- Has a history of malignant cancer within past 5 years, except for adequately treated basal cell or squamous cell skin cancer or cervical cancer.
- Has a history of hypersensitivity or reaction to more than 2 chemical classes of drugs, including prescription & over-the-counter medications.
- Is currently participati
Data sourced from ClinicalTrials.gov (NCT01564459). 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.