Simulated Driving Performance, Daytime Sedation and Cognition in Healthy Volunteers Taking Gralise, Neurontin or Lyrica

NCT03179345 — Phase 4, Completed, 32 participants, Depomed

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A Phase 4, Double-Blind, Placebo-Controlled, Crossover Study Comparing Simulated Driving Performance, Daytime Sedation, and Cognition in Healthy Volunteers Taking Therapeutic Doses of Gralise®, Neurontin®, or Lyrica®

RegistryNCT03179345
StatusCompleted
PhasePhase 4
Study typeInterventional; randomized, crossover, other
Enrollment32 (Actual)
SponsorDepomed (Industry)
ConditionsHealthy
InterventionsGabapentin, Pregabalin, Placebo (Drug, other)
Datesstart 2015-09-24, primary completion 2015-11-20, completion 2015-11-20, first posted 2017-06-07, last updated 2020-06-01

Related Papers Related Patents Related Grants Related Experts
All trials for Healthy All trials of Gabapentin All trials of Pregabalin

-Summary

Phase 4, double-blind, placebo-controlled, four treatment, four sequence crossover study comparing simulated driving performance, daytime sedation and cognition in healthy volunteers administered therapeutic doses of Gralise® (Treatment A), Neurontin® (Treatment B), Lyrica® (Treatment C) and placebo (Treatment D). All doses were administered under fed conditions.

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+Arms and interventions

ArmTypeInterventionsDescription
Gralise® (gabapentin)Active comparatorDrug: GabapentinGralise® 3 x 600 mg tablets (1800 mg total dose) administered once daily at 7:00 pm on Day 1 and Day 2 with one placebo capsule matching the over-encapsulation of doses of Neurontin® and Lyrica®. At other dosing times, treatment consisted of 3 placebo tablets matching the appearance of Gralise® and 1 placebo capsule.
Neurontin® (gabapentin)Active comparatorDrug: GabapentinNeurontin® 1 x 600 mg film-coated tablet administered 3 times daily at 7:00 pm on Day 1, at 8:00 am, 2:00 pm and 8:00 pm on Day 2 and at 8:00 a.m. on Day 3. Each dose of Neurontin® was over-encapsulated and administered with 3 placebo tablets matching the appearance of Gralise®.
Lyrica® (pregabalin)Active comparatorDrug: PregabalinLyrica® 1 x 150 mg capsule administered 2 times daily at 7:00 pm on Day 1, at 8:00 am and 8:00 pm on Day 2 and at 8:00 a.m. on Day 3. Each dose of Lyrica® was over-encapsulated and administered with 3 placebo tablets matching the appearance of Gralise®.
Placebo (sugar pill)Placebo comparatorOther: PlaceboEach dose consisted of 3 placebo tablets matching the appearance of Gralise® and 1 placebo capsule matching the over-encapsulation of doses of Neurontin® and Lyrica®.
  • Gabapentin (Drug), also known as Gralise®, Neurontin®
  • Pregabalin (Drug), also known as Lyrica®
  • Placebo (Other), also known as Sugar Pill

+Outcome measures

Primary outcomes

  • Change From Baseline in the "Standard Deviation of the Lateral Position" (SDLP) Measured on the Driving Simulator Between Gralise® and Neurontin® [Baseline and Hour 3 on Day 3]: SDLP (feet): This is a measurement of change from maintaining the normal driving position in the lane over time and / or distance.

Secondary outcomes

  • Change From Baseline in the "Standard Deviation of the Lateral Position" (SDLP) Measured on the Driving Simulator Between Gralise® and Lyrica® [Baseline and Hour 3 on Day 3]: SDLP (feet): This is a measurement of change from maintaining the normal driving position in the lane over time and / or distance.
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Cognitive Evaluation of Cogstate - Detection Task (DET) [Baseline and Hour 3 on Day 3]: Cogstate - Detection Task (DET) is a simple reaction time test of Psychomotor Function. Higher change from baseline means better performance.
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Cognitive Evaluation of Cogstate - Groton Maze Learning Test (GMLT). [Baseline and Hour 3 on Day 3]: Cogstate - The Groton Maze Learning test is a measure Executive Function. Total number of errors made while attempting to learn the same hidden pathway across the consecutive learning trials performed at a single assessment. Lower score means better performance. Higher change from baseline means better performance.
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Cognitive Evaluation of Cogstate - Identification Task (IDN). [Baseline and Hour 3 on Day 3]: Cogstate - Identification Task (IDN) assesses Attention. Score is speed of performance (mean of the log10 transformed reaction times for correct responses). Lower score (quicker speed) is better performance. Higher change from baseline means better performance.
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Cognitive Evaluation of Cogstate - International Shopping List Test (ISL) [Baseline and Hour 3 on Day 3]: Cogstate - International Shopping List (ISL) test is a measure of verbal learning and uses a well-validated list-learning paradigm. Total number of correct responses remembering the word list on three consecutive trials at a single assessment. Higher score is better performance. Higher change from baseline means better performance.
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Cognitive Evaluation of Cogstate - One Card Learning (OCLT). [Baseline and Hour 3 on Day 3]: Cogstate - The One Card Learning Test (OCLT) is a measure of visual learning and uses a well-validated pattern separation paradigm with playing card stimuli. Higher Score is better performance. Higher change from baseline means better performance.
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Sedation Evaluation - Karolinska Sleepiness Scale (KSS). [Baseline and Hour 3 on Day 3]: Scale: 1-9, 1=extremely alert, 9 = very sleepy, great effort to keep awake, fighting sleep
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Sedation Evaluation - Portland Neurotoxicity Scale (PNS). [Baseline and Hour 3 on Day 3]: Portland Neurotoxicity Scale (PNS) comprises 15 questions measured on a 10-point scale. \[1=No problem, 2, 3, 4, 5=Often a problem, 6, 7, 8, 9, 10=Severe problem\] in 16 categories. Each question was analyzed and is presented in the same way as the primary endpoints.
  • Change From Baseline Between Gralise® and Neurontin® in the Driving Simulator - Standard Deviation of Vehicle Speed (SDVS). [Baseline and Hour 3 on Day 3]: Miles per Hour (mph)
  • Change From Baseline Between Gralise® and Lyrica® in the Driving Simulator - Standard Deviation of Vehicle Speed (SDVS). [Baseline and Hour 3 on Day 3]: Miles per Hour (mph)
  • To Compare the Relative Safety and Tolerability of Gralise®, Neurontin®, and Lyrica®. [Screening to 1 week after Period 4 discharge]: * Number of subjects with Treatment-Emergent Adverse Events (TEAE) * Number of subjects with Serious Adverse Event (SAE) * Number of subjects discontinued due to Adverse Event (AE)

+Eligibility

Sex: All, ages: 40 Years to 80 Years, accepts healthy volunteers

Inclusion Criteria:

* Between 40 and 80 years of age, inclusive.
* Body weight > 50 kg and BMI between 18 and 32 kg/m2, inclusive.
* Able to give informed consent.
* Licensed, experienced driver who had driven at least 3 times a week for the past 3 years and had visual acuity adequate for driving, as assessed by the investigator or designee.
* Able to complete a 1 hour simulated driving test and demonstrate satisfactory driving skills, as determined by the investigator or designee.
* Karolinska Sleep Scale (KSS) score of <=5.
* Other criteria apply.

Exclusion Criteria:

* Known history of allergic reaction, hypersensitivity or clinically significant intolerance to gabapentin, pregabalin or any pharmaceutical materials, or any of the ingredients in the protocol-specified meals.
* Pregnant or lactating or considered at risk of pregnancy.
* Any medical condition or any laboratory abnormality or ECG abnormality that would, in the opinion of the investigator, contraindicate study participation.
* Impaired liver function (e.g., alanine aminotransferase \[ALT\] ≥2 times the upper limit of normal \[ULN\] or bilirubin ≥2 times ULN), known active hepatic disease (e.g., hepatitis), or evidence of clinically significant liver disease or other condition affecting the liver that may suggest the potential for an increased susceptibility to hepatic toxicity with oral gabapentin or pregabalin exposure.
* Any history of renal disease that, in the opinion of the investigator, would contraindicate study participation; or subject had significantly impaired renal function as evidenced by an estimated GFR of ≤ 80 ml/min/1.73m2.
* History or evidence of a sleep disorder, including sleep apnea (obstructive, central or mixed), narcolepsy or primary insomnia.
* Other criteria apply.

+Posted results

Participant flow

MilestoneGral First, Then Neur, Lyr, and PlboNeur First, Then Plbo, Gral, and LyrLyr First, Then Gral, Plbo, and NeurPlbo First, Then Lyr, Neur, and Gral
Started8888
Received gralise®8776
Received neurontin®8878
Received lyrica®8788
Received placebo8778
Completed8776
Not completed0112

Outcome results

  • Change From Baseline in the "Standard Deviation of the Lateral Position" (SDLP) Measured on the Driving Simulator Between Gralise® and Neurontin® (Primary), Least squares mean, feet: Gralise® (Gabapentin) 0.255 +/- 0.0781; Neurontin® (Gabapentin) 0.395 +/- 0.0763; Placebo 0.135 +/- 0.0770 (p 0.0275)
  • Change From Baseline in the "Standard Deviation of the Lateral Position" (SDLP) Measured on the Driving Simulator Between Gralise® and Lyrica® (Secondary), Least squares mean, feet: Gralise® (Gabapentin) 0.255 +/- 0.0781; Lyrica® (Pregabalin) 0.356 +/- 0.0770; Placebo 0.135 +/- 0.0770 (p 0.1103)
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Cognitive Evaluation of Cogstate - Detection Task (DET) (Secondary), Least squares mean, msec: Gralise® (Gabapentin) 0.00 +/- 0.013; Neurontin® (Gabapentin) 0.00 +/- 0.012; Lyrica® (Pregabalin) -0.01 +/- 0.012; Placebo (Sugar Pill) -0.00 +/- 0.012 (p 0.9946)
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Cognitive Evaluation of Cogstate - Groton Maze Learning Test (GMLT). (Secondary), Least squares mean, Number of errors on test: Gralise® (Gabapentin) -0.40 +/- 2.484; Neurontin® (Gabapentin) -0.01 +/- 2.385; Lyrica® (Pregabalin) -0.64 +/- 2.419; Placebo (Sugar Pill) 3.32 +/- 2.420 (p 0.8799)
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Cognitive Evaluation of Cogstate - Identification Task (IDN). (Secondary), Least squares mean, Score on Scale: Gralise® (Gabapentin) -0.00 +/- 0.000; Neurontin® (Gabapentin) 0.00 +/- 0.000; Lyrica® (Pregabalin) -0.00 +/- 0.000; Placebo (Sugar Pill) 0.01 +/- 0.000 (p 0.7111)
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Cognitive Evaluation of Cogstate - International Shopping List Test (ISL) (Secondary), Least squares mean, Score on Scale: Gralise® (Gabapentin) 0.36 +/- 0.684; Neurontin® (Gabapentin) 0.82 +/- 0.648; Lyrica® (Pregabalin) 0.03 +/- 0.660; Placebo (Sugar Pill) -0.01 +/- 0.660 (p 0.5950)
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Cognitive Evaluation of Cogstate - One Card Learning (OCLT). (Secondary), Least squares mean, Score on Scale: Gralise® (Gabapentin) 0.02 +/- 0.021; Neurontin® (Gabapentin) 0.06 +/- 0.020; Lyrica® (Pregabalin) 0.00 +/- 0.020; Placebo (Sugar Pill) 0.03 +/- 0.020 (p 0.0070)
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Sedation Evaluation - Karolinska Sleepiness Scale (KSS). (Secondary), Least squares mean, units on a scale: Gralise® (Gabapentin) .774 +/- .2985; Neurontin® (Gabapentin) .264 +/- .2876; Lyrica® (Pregabalin) .868 +/- .2913; Placebo (Sugar Pill) .264 +/- .2914 (p 0.1026)
  • Change From Baseline Between, Gralise® and Neurontin®, Gralise® and Lyrica® for Sedation Evaluation - Portland Neurotoxicity Scale (PNS). (Secondary), Least squares mean, scores on a scale: Gralise® (Gabapentin) 0.036 +/- 0.1274; Neurontin® (Gabapentin) 0.322 +/- 0.1235; Lyrica® (Pregabalin) 0.249 +/- 0.1249; Placebo (Sugar Pill) 0.115 +/- 0.1249 (p 0.0177)
  • Change From Baseline Between Gralise® and Neurontin® in the Driving Simulator - Standard Deviation of Vehicle Speed (SDVS). (Secondary), Least squares mean, mph: Gralise® (Gabapentin) 0.831 +/- 0.4844; Neurontin® (Gabapentin) 0.947 +/- 0.4648; Placebo 0.851 +/- 0.4715 (p 0.8293)
  • Change From Baseline Between Gralise® and Lyrica® in the Driving Simulator - Standard Deviation of Vehicle Speed (SDVS). (Secondary), Least squares mean, mph: Gralise® (Gabapentin) 0.831 +/- 0.4844; Lyrica® (Pregabalin) 1.319 +/- 0.4713; Placebo 0.851 +/- 0.4715 (p 0.3666)
  • To Compare the Relative Safety and Tolerability of Gralise®, Neurontin®, and Lyrica®. (Secondary), Number, participants: Gralise® (Gabapentin) 6; Neurontin® (Gabapentin) 13; Lyrica® (Pregabalin) 16; Placebo (Sugar Pill) 5

Adverse events

Time frame: 7 weeks

ArmDeathsSerious adverse eventsOther adverse events
Gralise® (Gabapentin)00/28 (0.0%)6/28 (21.4%)
Neurontin® (Gabapentin)00/31 (0.0%)11/31 (35.5%)
Lyrica® (Pregabalin)00/31 (0.0%)14/31 (45.2%)
Placebo (Sugar Pill)00/30 (0.0%)2/30 (6.7%)

Other adverse events by term

TermOrgan systemGralise® (Gabapentin)Neurontin® (Gabapentin)Lyrica® (Pregabalin)Placebo (Sugar Pill)
SomnolenceNervous system disorders3/287/314/311/30
DizzinessNervous system disorders3/284/316/310/30
HeadacheNervous system disorders1/280/315/311/30
Euphoric moodPsychiatric disorders1/282/313/310/30

+Publications

  • Results publication: Schmidt P, Rao S. Effects of gabapentin, pregabalin and gastroretentive gabapentin on simulated driving, daytime sedation and cognition. Pain Manag. 2018 Jul 1;8(4):297-306. doi: 10.2217/pmt-2018-0005. Epub 2018 Apr 19. PMID 29671676

+Investigators

  • Head of R&D, Study director, Depomed