Samidorphan Explained
Samidorphan (developmental code names ALKS-33, RDC-0313) is an opioid antagonist that in the form of olanzapine/samidorphan (brand name Lybalvi) is used in the treatment of schizophrenia and bipolar disorder.[1] [2] Samidorphan reduces the weight gain associated with olanzapine.[3] [4] Samidorphan is taken by mouth.[5]
Samidorphan was under development as a standalone medication for various indications but has been discontinued.[6] Buprenorphine/samidorphan for the treatment of major depressive disorder was rejected by the Food and Drug Administration due to insufficient evidence of effectiveness but remains in preregistration as of September 2021.[7] Development of baclofen/samidorphan has also been discontinued.[8]
Development
Samidorphan has been investigated for the treatment of alcoholism and cocaine addiction by its developer, Alkermes,[9] showing similar efficacy to naltrexone but possibly with reduced side effects.
However, it has attracted much more attention as part of the combination product ALKS-5461 (buprenorphine/samidorphan), where samidorphan is combined with the mixed μ-opioid receptor (MOR) weak partial agonist and κ-opioid receptor (KOR) antagonist buprenorphine, as an antidepressant. Buprenorphine has shown antidepressant effects in some human studies, thought to be because of its antagonist effects at the KOR, but has not been further developed for this application because of its MOR agonist effects and consequent abuse potential. By combining buprenorphine with samidorphan to block the MOR agonist effects, the combination acts more like a selective KOR antagonist, and produces only antidepressant effects, without typical MOR effects such as euphoria or substance dependence being evident.[10] [11]
Samidorphan was also studied in combination with olanzapine, as ALKS-3831 (olanzapine/samidorphan), for use in schizophrenia.[12] A Phase 3 study found that the addition of samidorphan to olanzapine significantly reduced weight gain compared to olanzapine alone,[13] and the combination was approved for the treatment of schizophrenia and bipolar disorder by the US Food and Drug Administration in May 2021, under the brand name Lybalvi.[14] [15]
Side effects
Side effects of samidorphan include somnolence and gastrointestinal disturbances among others.
Pharmacology
Pharmacodynamics
Samidorphan at the opioid receptors[16] [17] ! Receptor! Ki! EC50! Emax! IC50! Imax | 0.052 nM | – | 3.8% | 0.88 nM | 92% |
| 0.23 nM | 3.3 nM | 36% | 38 nM | 57% |
| 2.6 nM | 1.5 nM | 35% | 6.9 nM | 56% | |
Samidorphan acts primarily as an antagonist or very weak partial agonist of the μ-opioid receptor (MOR) and to a lesser extent as a partial agonist of the κ-opioid receptor (KOR) and δ-opioid receptor (DOR). In accordance with this profile, samidorphan has been observed to produce some side effects that are potentially consistent with activation of the KOR such as somnolence, sedation, dizziness, and hallucinations in some patients in clinical trials.[18]
Pharmacokinetics
The elimination half-life of samidorphan is 7 to 9 hours.
Chemistry
Samidorphan has its origins in academia where 8-carboxamidocyclazocine and naltrexone were utilized in its design and synthesis.[19]
External links
Notes and References
- Chaudhary AM, Khan MF, Dhillon SS, Naveed S . A Review of Samidorphan: A Novel Opioid Antagonist . Cureus . 11 . 7 . e5139 . July 2019 . 31523568 . 6741386 . 10.7759/cureus.5139 . free .
- Web site: Olanzapine/samidorphan - Alkermes plc . Adis Insight . Springer Nature Switzerland AG .
- Citrome L, Graham C, Simmons A, Jiang Y, Todtenkopf MS, Silverman B, DiPetrillo L, Cummings H, Sun L, McDonnell D . 6 . An Evidence-Based Review of OLZ/SAM for Treatment of Adults with Schizophrenia or Bipolar I Disorder . Neuropsychiatric Disease and Treatment . 17 . 2885–2904 . 2021 . 34526769 . 8437420 . 10.2147/NDT.S313840 . free .
- Paik J . Olanzapine/Samidorphan: First Approval . Drugs . 81 . 12 . 1431–1436 . August 2021 . 34304374 . 10.1007/s40265-021-01568-0 . 236215923 .
- Web site: LYBALVI: Highlight of Prescribing Information . U.S. Food and Drug Administration .
- Web site: Samidorphan . Adis Insight . Springer Nature Switzerland AG .
- Web site: Buprenorphine/samidorphan - Alkermes . Adis Insight . Springer Nature Switzerland AG .
- Web site: Baclofen/samidorphan . Adis Insight . Springer Nature Switzerland AG .
- Hillemacher T, Heberlein A, Muschler MA, Bleich S, Frieling H . Opioid modulators for alcohol dependence . Expert Opinion on Investigational Drugs . 20 . 8 . 1073–1086 . August 2011 . 21651459 . 10.1517/13543784.2011.592139 . 43338618 .
- Web site: ALKS 5461 drug found to reduce depressive symptoms in Phase 1/2 study . 30 May 2012 .
- Web site: Investigational ALKS 5461 Channels 'Opium Cure' for Depression .
- News: John . LaMattina . vanc . 15 January 2013 . Will Alkermes' Antipsychotic ALKS-3831 Become Another Tredaptive? . Forbes.
- Correll CU, Newcomer JW, Silverman B, DiPetrillo L, Graham C, Jiang Y, Du Y, Simmons A, Hopkinson C, McDonnell D, Kahn RS . 6 . Effects of Olanzapine Combined With Samidorphan on Weight Gain in Schizophrenia: A 24-Week Phase 3 Study . The American Journal of Psychiatry . 177 . 12 . 1168–1178 . December 2020 . 32791894 . 10.1176/appi.ajp.2020.19121279 . 221122225 .
- Web site: Lybalvi: FDA-Approved Drugs . U.S. Food and Drug Administration (FDA) . 1 June 2021.
- News: Ergenzinger. Ed. New Antipsychotic Combo for Bipolar Disorder Approved by FDA Psychology Today. 2021-07-24. www.psychologytoday.com. en.
- Book: Linda P. Dwoskin. Emerging Targets & Therapeutics in the Treatment of Psychostimulant Abuse. 29 January 2014. Elsevier Science. 978-0-12-420177-4. 398–399, 402–403.
- Wentland MP, Lou R, Lu Q, Bu Y, Denhardt C, Jin J, Ganorkar R, VanAlstine MA, Guo C, Cohen DJ, Bidlack JM . 6 . Syntheses of novel high affinity ligands for opioid receptors . Bioorganic & Medicinal Chemistry Letters . 19 . 8 . 2289–2294 . April 2009 . 19282177 . 2791460 . 10.1016/j.bmcl.2009.02.078 .
- McElroy SL, Guerdjikova AI, Blom TJ, Crow SJ, Memisoglu A, Silverman BL, Ehrich EW . A placebo-controlled pilot study of the novel opioid receptor antagonist ALKS-33 in binge eating disorder . The International Journal of Eating Disorders . 46 . 3 . 239–245 . April 2013 . 23381803 . 10.1002/eat.22114 . free .
- Wentland MP, Lu Q, Lou R, Bu Y, Knapp BI, Bidlack, JM . Synthesis and opioid receptor binding properties of a highly potent 4-hydroxy analogue of naltrexone . Bioorganic & Medicinal Chemistry Letters . 15 . 8 . 2107–10 . April 2005 . 15808478 . 10.1016/j.bmcl.2005.02.032 .