Pharmacodynamic and pharmacokinetic evaluation of buprenorphine + samidorphan for the treatment of major depressive disorder.
Renee-Marie RagguettCarola RongJoshua D RosenblatRoger C HoRoger S McIntyrePublished in: Expert opinion on drug metabolism & toxicology (2018)
Treatment resistant depression (TRD) represents approximately 20% of all individuals receiving care for major depressive disorder. The opioidergic system is identified as a novel target which hitherto has not been sufficiently investigated in adults with TRD. The combination product buprenorphine + samidorphan is an opioid modulatory agent which has demonstrated replicated evidence of efficacy in TRD without abuse liability. Areas covered: Databases Pubmed, Google Scholar and clinicaltrials.gov were searched from inception through December 2017 for clinical trial information, pharmacokinetics, and pharmacodynamics of buprenorphine + samidorphan. Herein we provide a summary of the available information. Eight clinical trials were identified for inclusion, of the eight trials, five trials had available results and are included in detail in our review. Expert opinion: Buprenorphine + samidorphan has demonstrated efficacy in TRD. Extant evidence surrounding the safety and tolerability profile of buprenorphine + samidorphan does not identify any significant safety concerns. Additional studies are needed in order to assess the long-term safety and efficacy of this product.
Keyphrases
- major depressive disorder
- clinical trial
- bipolar disorder
- open label
- pain management
- healthcare
- double blind
- phase ii
- chronic pain
- depressive symptoms
- health information
- quality improvement
- mass spectrometry
- phase iii
- big data
- clinical practice
- sleep quality
- social media
- placebo controlled
- replacement therapy
- high speed