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Combining Pregabalin (LYRICA®) With Lofexidine (LUCEMYRATM) to Treat OPIOID Withdrawal (PGB-LOF)

Primary Purpose

Opioid Withdrawal

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Pregabalin 200 MG capsules
Placebo oral tablet
Lofexidine 0.18Mg Tab
Sponsored by
University of Pennsylvania
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opioid Withdrawal

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male and/or female subjects ≥ 18 years of age
  2. Meet DSM-5 criteria for an Opioid Use Disorder with physiologic features. Have 2 or more of the 11 DSM 5 criteria for opioid disorder including tolerance and withdrawal features in the last 12 months
  3. Interested in opioid antagonist treatment
  4. Have used opioids in 20 or more of the last 30 days
  5. Have a stable address in the local area; not planning to move; have documents for ID check
  6. Absence of medical or psychiatric conditions that are likely to interfere with study participation
  7. Have a 12 lead ECG demonstrating a QTc ≤450 msec and a QRS interval ≤120 msec. The site PI has the final determination for inclusion into the study for ECGs unless there is a question of QT prolongation or other factors (QTc/Fre uses the Frederica formula (QTc = QT/RR(1/3)). If consultation is needed, the PENN cardiologists and the medical monitor should be contacted
  8. If female, have a negative pregnancy test and uses adequate contraception if of childbearing potential

Exclusion Criteria:

  1. Current psychotic disorder (bipolar I, schizophrenia, major depression with psychotic features,) as defined by the MINI
  2. An alcohol, benzodiazepine, or other sedative use disorder with physiological features that require medication for detoxification
  3. History of allergy or other serious adverse event due to treatment with pregabalin, XR-NTX, or lofexidine
  4. Pending incarceration in the next 30 days
  5. Homicidal or otherwise behaviorally disturbed requiring immediate attention.
  6. High Risk for suicide as determined by answering 'yes' to questions 4 and/or 5 on C-SSRS at screening
  7. Blood pressure <90 mm Hg (systolic) or <60 mm Hg (diastolic). If this value is out of normal range, the investigator and a study clinician will decide subject inclusion or exclusion on a case-by-case basis
  8. Heart rate and/or pulse<50 bpm at screening-sitting
  9. An Estimated Glomerular Filtration Rate eGFR<90 mL/min/1.73m2
  10. A History of, or current Seizure disorder (excluding childhood febrile seizures)
  11. Inability to read and/or understand English. For example, unable to understand the informed consent as demonstrated by failing to answer 9/10 questions correctly on the quiz
  12. Pregnant or breastfeeding
  13. Currently taking sympathomimetic drugs, or a thiazolidinedione antidiabetic
  14. An ALT and/or AST test that is at >4X the top limit of normal
  15. A Child-Pugh score >7
  16. Currently receiving opioids for pain management
  17. In a treatment study where medication was administered in the last 30 days
  18. Currently using medications that are known to be strong or moderate inhibitors of CYP2D6 such as fluoxetine, paroxetine, mirabegron, bupropion, quinidine, terbinafine, cimetidine, cinacalcet, duloxetine, or fluvoxamine
  19. In a methadone maintenance or buprenorphine treatment program within the last 30 days

Sites / Locations

  • Mountain Manor Treatment Center
  • John Mariani
  • Treatment Research Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

PGB/LFX;

Lofexidine and PLACEBO

Arm Description

0.54 mg lofexidine and 200 mg Pregabalin on days 1 -7 with taper for pregabalin and lofexidine starting on day 5

0.54 mg lofexidine and Placebo (PLB) on days 1-7 with taper for lofexidine starting on day 5

Outcomes

Primary Outcome Measures

withdrawal
reduction of withdrawal

Secondary Outcome Measures

complete detoxification
Proportion of subjects who complete the 7 day detoxification

Full Information

First Posted
January 2, 2020
Last Updated
April 12, 2023
Sponsor
University of Pennsylvania
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1. Study Identification

Unique Protocol Identification Number
NCT04218240
Brief Title
Combining Pregabalin (LYRICA®) With Lofexidine (LUCEMYRATM) to Treat OPIOID Withdrawal
Acronym
PGB-LOF
Official Title
Combining Pregabalin (LYRICA®) With Lofexidine (LUCEMYRATM): Can it Increase the Success of Transition to Naltrexone?
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
December 20, 2020 (Actual)
Primary Completion Date
March 23, 2023 (Actual)
Study Completion Date
March 23, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pennsylvania

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A phase II double-blind placebo-controlled parallel group clinical trial that will randomize 90 subjects to investigate whether pregabalin (PGB) combined with Lofexidine (LFX) can reduce opioid withdrawal-related subjective effects, and investigate, whether the PGB/LFX combination can increase the proportion of patients with an opioid use disorder (OUD) who complete detoxification and transition to antagonist treatment with extended-release injectable naltrexone (XR-NTX).
Detailed Description
An inpatient detoxification study where pregabalin (PBG) will be given orally at a starting dose of up to 600 mg daily (group 1) tapered to 100 mg daily over 7 days; given with lofexidine (LFX) starting at 2.16 mg daily and declining to 0.72 mg over 7 days. On day 8, subjects are offered an injection of XR-NTX if they provide a urine sample that is negative for opioids and buprenorphine and pass a naloxone challenge. All subjects, regardless of whether or not they receive XR-NTX, will be given a referral and appointment for follow-up treatment when they leave the inpatient detoxification program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Withdrawal

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
for the primary comparison of longitudinal subjective withdrawal measures, comparing the groups on rate of decrease across detox days, using a linear group by time effect for the mixed effects models described above. We have one primary outcome, so use an alpha level of 0.05, and we use two-sided tests. 90 subjects, 30 from each of three sites, who will be randomized into two groups, with 30 assigned to Lofexidine plus Placebo, and 60 to Lofexidine plus a starting daily dose of 400 mg of pregabalin and increasing to 600mg Pregabalin on day 2.
Masking
ParticipantCare ProviderInvestigator
Masking Description
The Penn Investigational Drug Service (IDS) will prepare blinded pregabalin capsules by over encapsulation of the drug into capsules shells matching the placebo capsules. Blinded pregabalin capsules will be packaged into blister packs along with lofexidine tablets, in separate compartments that are labeled for dosing times on days 1-7 and ship them to the research sites.
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
PGB/LFX;
Arm Type
Experimental
Arm Description
0.54 mg lofexidine and 200 mg Pregabalin on days 1 -7 with taper for pregabalin and lofexidine starting on day 5
Arm Title
Lofexidine and PLACEBO
Arm Type
Active Comparator
Arm Description
0.54 mg lofexidine and Placebo (PLB) on days 1-7 with taper for lofexidine starting on day 5
Intervention Type
Drug
Intervention Name(s)
Pregabalin 200 MG capsules
Other Intervention Name(s)
lyrica
Intervention Description
oral pregabalin 200 mg capsules given with a taper on day 5
Intervention Type
Drug
Intervention Name(s)
Placebo oral tablet
Intervention Description
oral Placebo
Intervention Type
Drug
Intervention Name(s)
Lofexidine 0.18Mg Tab
Other Intervention Name(s)
lucemyra
Intervention Description
lofexidine 0.18 tab given with a taper starting on day 5
Primary Outcome Measure Information:
Title
withdrawal
Description
reduction of withdrawal
Time Frame
7 days
Secondary Outcome Measure Information:
Title
complete detoxification
Description
Proportion of subjects who complete the 7 day detoxification
Time Frame
7 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and/or female subjects ≥ 18 years of age Meet DSM-5 criteria for an Opioid Use Disorder with physiologic features. Have 2 or more of the 11 DSM 5 criteria for opioid disorder including tolerance and withdrawal features in the last 12 months Interested in opioid antagonist treatment Have used opioids in 20 or more of the last 30 days Have a stable address in the local area; not planning to move; have documents for ID check Absence of medical or psychiatric conditions that are likely to interfere with study participation Have a 12 lead ECG demonstrating a QTc ≤450 msec and a QRS interval ≤120 msec. The site PI has the final determination for inclusion into the study for ECGs unless there is a question of QT prolongation or other factors (QTc/Fre uses the Frederica formula (QTc = QT/RR(1/3)). If consultation is needed, the PENN cardiologists and the medical monitor should be contacted If female, have a negative pregnancy test and uses adequate contraception if of childbearing potential Exclusion Criteria: Current psychotic disorder (bipolar I, schizophrenia, major depression with psychotic features,) as defined by the MINI An alcohol, benzodiazepine, or other sedative use disorder with physiological features that require medication for detoxification History of allergy or other serious adverse event due to treatment with pregabalin, XR-NTX, or lofexidine Pending incarceration in the next 30 days Homicidal or otherwise behaviorally disturbed requiring immediate attention. High Risk for suicide as determined by answering 'yes' to questions 4 and/or 5 on C-SSRS at screening Blood pressure <90 mm Hg (systolic) or <60 mm Hg (diastolic). If this value is out of normal range, the investigator and a study clinician will decide subject inclusion or exclusion on a case-by-case basis Heart rate and/or pulse<50 bpm at screening-sitting An Estimated Glomerular Filtration Rate eGFR<90 mL/min/1.73m2 A History of, or current Seizure disorder (excluding childhood febrile seizures) Inability to read and/or understand English. For example, unable to understand the informed consent as demonstrated by failing to answer 9/10 questions correctly on the quiz Pregnant or breastfeeding Currently taking sympathomimetic drugs, or a thiazolidinedione antidiabetic An ALT and/or AST test that is at >4X the top limit of normal A Child-Pugh score >7 Currently receiving opioids for pain management In a treatment study where medication was administered in the last 30 days Currently using medications that are known to be strong or moderate inhibitors of CYP2D6 such as fluoxetine, paroxetine, mirabegron, bupropion, quinidine, terbinafine, cimetidine, cinacalcet, duloxetine, or fluvoxamine In a methadone maintenance or buprenorphine treatment program within the last 30 days
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stuart Watson
Organizational Affiliation
Office of Research Administration, Univ. of Pennsylvania
Official's Role
Study Director
Facility Information:
Facility Name
Mountain Manor Treatment Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21229
Country
United States
Facility Name
John Mariani
City
New York
State/Province
New York
ZIP/Postal Code
10019
Country
United States
Facility Name
Treatment Research Center
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Not at this time

Learn more about this trial

Combining Pregabalin (LYRICA®) With Lofexidine (LUCEMYRATM) to Treat OPIOID Withdrawal

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