Literature DB >> 32099511

Erratum: Depot Buprenorphine Injection in the Management of Opioid Use Disorder: From Development to Implementation [Corrigendum].

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Abstract

[This corrects the article DOI: 10.2147/SAR.S155843.].
© 2020 Ling et al.

Entities:  

Year:  2020        PMID: 32099511      PMCID: PMC7002736          DOI: 10.2147/SAR.S247083

Source DB:  PubMed          Journal:  Subst Abuse Rehabil        ISSN: 1179-8467


Ling W, Shoptaw S, Goodman-Meza D. Subst Abuse Rehabil. 2019;10:69–78. The authors of this paper have advised that Table 1 is incorrect. The authors advised that they had listed values for Cmax and Ctrough after a single dose of Brixadi (CAM2038) and not steady state, as it was provided for Sublocade. The new Table 1 reflects the Brixadi steady state concentrations for a more direct comparison with Sublocade.
Table 1

Comparison of Long-Acting Formulations of Buprenorphine FDA-Approved for Treatment of Opioid Use Disorder

Brand NameProbuphineSublocadeBrixadi (US) or Buvidal (Europe/Australia)
Molecular nameRBP-6000CAM2038
PharmaceuticalPreviously Braeburn, currently TitanIndiviorBraeburn Pharmaceuticals/Camurus
Indicated populationStable transmucosal buprenorphine dose of 8 mg or less for three months or longerInitiated transmucosal buprenorphine (8–24 mg) for a minimum of 7 days.Initiation of treatment in patients not already receiving buprenorphine or switching from transmucosal buprenorphine
Route of administrationSubcutaneous implantSubcutaenous injectionSubcutaenous injection
Duration of effect6 months1 month1 week or 1 month
Dosage320 mg (Four 80 mg implants)100 and 300 mg8, 16, 24 and 32 mg (weekly) or 64, 96 and 128 mg (monthly)
Long acting technologyEthylene vinyl acetate (EVA) polymer18% (weight/weight) buprenorphine base in the ATRIGEL Delivery SystemProlonged release FluidCrystal injection depot technology
LocationUpper armAbdomenButtock, thigh, stomach (abdomen) or upper arm
FDA-approval201620172018 (tentative)
Plasma concentrations (ng/mL)CmaxCmaxCmax
3.234.88 (100 mg)Weekly 4.3–6.9
10.12 (300 mg)Monthly 4.0–11.1
CtroughCtroughCtrough
0.722.48 (100 mg)Weekly 0.8–2.6
5.01 (300 mg)Monthly 1.3–2.1
Provider burden+++++++
Live training programSupervised injectionSupervised injection
Procedural competencyMonthly injectionsWeekly or monthly injections
Special Handling RequirementsRequires implant procedureNeeds RefrigerationNo special requirements
Need for removal or replacement every 6 monthsInjection only under skin around umbilicus
Comparison of Long-Acting Formulations of Buprenorphine FDA-Approved for Treatment of Opioid Use Disorder The correct Table 1 is as follows:
  1 in total

1.  Increased Treatment Engagement and Adherence: Flexible Management with Prolonged-Release Buprenorphine in Treatment of Opioid Dependence.

Authors:  Bernadette Hard
Journal:  Case Rep Psychiatry       Date:  2021-02-27
  1 in total

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