In a indirect treatment analysis, oliceridine statistically significantly reduced the incidence of nausea and/or vomiting or the need for antiemetics in orthopedic surgery compared to hydromorphone and a non-statistically significant numerical trend toward reduced nausea and/or vomiting versus fentanyl.
Joseph Biskupiak, Gary Oderda, Diana Brixner, Todd L Wandstrat
View PDFA comparison of the neurocognitive (sedation and body orientation) effects of oliceridine versus morphine including the more rapid onset and offset of neurocognitive effects for oliceridine and a smaller magnitude of neurocognitive effects over time.
Laurence Moss, M.D., Hemme Hijma, Ph.D., Mark Demitrack, M.D., Jessica Kim, M.Sc., Geert Jan Groeneveld, M.D., Ph.D., Monique van Velzen, Ph.D., Marieke Niesters, M.D., Ph.D., Erik Olofsen, Ph.D., Albert Dahan, M.D., Ph.D.
View PDFOliceridine for the Management of Moderate to Severe Acute Postoperative Pain: A Narrative Review
Conventional opioid analgesics, such as morphine, fentanyl, and hydromorphone, are mainstays of acute pain management; however, their use is accompanied by well-known opioid related adverse events (ORAEs), nausea, vomiting, and central nervous system effects. Oliceridine demonstrated analgesic efficacy superior to placebo and comparable to morphine, with favorable results on reduction of ORAEs.
Neil Daksla, Ashley Wang, Zhaosheng Jin, Abhishek Gupta, Sergio Bergese
View WebsiteA comparison of the respiratory effects of Oliceridine versus morphine including the more rapid onset and offset of respiratory depression for oliceridine and a smaller magnitude of respiratory depression over time.
Pieter Simons, M.D., Rutger van der Schrier, M.D., Maarten van Lemmen, B.Sc., Simone Jansen, M.D., Kiki W.K. Kuijpers, B.Sc., Monique van Velzen, Ph.D., Elise Sarton, M.D., Ph.D., Todd Nicklas, M.S.N., Cathy Michalsky, M.Sc., Mark A. Demitrack, M.D., Michael Fossler, Pharm.D., Ph.D., F.C.P., Erik Olofsen, Ph.D., Marieke Niesters, M.D., Ph.D., Albert Dahan, M.D. Ph.D.
Anesthesiology 2023; 138:249–63
View PDFExpert Review on the Clinical Profile of Oliceridine in Post-Operative Care
Review highlights the strength of the evidence base for the safety and efficacy of Oliceridine and also elucidates the practical clinical importance of the responder rate used as the primary outcome measure in the randomized controlled pivotal Phase 3 APOLLO trials
Viscusi ER. A critical review of oliceridine injection as an IV opioid analgesic for the management of severe acute pain. Expert Rev Neurother. 2022 May 17:1-8. doi: 10.1080/14737175.2022.2072731. Epub ahead of print.
View WebsiteHealth Economic Models- Model in high-risk (elderly/obese) patients and Budget Impact model
Budget impact and pharmacy costs with targeted use of oliceridine for postsurgical pain in patients at high risk of opioid-related adverse events
Kit N Simpson, Michael J Fossler, Linda Wase, Mark A Demitrack, Todd L Wandstrat
View WebsiteOliceridine Exhibits Improved Tolerability Compared to Morphine at Equianalgesic Conditions: Exploratory Analysis from Two Phase 3 Randomized Placebo and Active Controlled Trials
Gregory B. Hammer, Ashish K. Khanna, Cathy Michalsky, Linda Wase, Mark A. Demitrack, Roderick Little, Michael J. Fossler & Sabry Ayad
View WebsiteHealth economic model – base case
Cost–effectiveness and cost-benefit analysis of oliceridine in the treatment of acute pain
Kit N Simpson, Michael J Fossler, Linda Wase & Mark A Demitrack
View WebsiteLow Incidence of Opioid-Induced Respiratory Depression Observed with Oliceridine Regardless of Age or Body Mass Index: Exploratory Analysis from a Phase 3 Open-Label Trial in Postsurgical Pain
Marek Brzezinski, Gregory B. Hammer, Keith A. Candiotti, Sergio D. Bergese, Peter H. Pan, Michael H. Bourne, Cathy Michalsky, Linda Wase, Mark A. Demitrack, Ashraf S. Habib. Pain & Therapy 2021.
View WebsiteReview of the efficacy and safety of intravenous oliceridine in the treatment of moderate to severe acute pain
Oliceridine in the treatment of moderate to severe acute pain
Sarada S Eleswarpu & Ashraf S Habib. Future Medicine 2021.
DOI: 10.2217/pmt-2020-0087
Oliceridine is Associated with Reduced Risk of Vomiting and Need for Rescue Antiemetics Compared to Morphine: Exploratory Analysis from Two Phase 3 Randomized Placebo and Active Controlled Trials
Timothy L. Beard, Cathy Michalsky, Keith A. Candiotti, Paul Rider, Linda Wase, Ashraf S. Habib, Mark A. Demitrack, Michael J. Fossler, Eugene R. Viscusi
View WebsiteBenefit and Risk Evaluation of Biased μ-Receptor Agonist Oliceridine versus Morphine.
Benefit and Risk Evaluation of Biased μ-Receptor Agonist Oliceridine versus Morphine.
Albert Dahan, C. Jan van Dam, Marieke Niesters, Monique van Velzen, Michael J. Fossler, Mark A. Demitrack, Erik Olofsen. Anesthesiology 2020. doi:
View WebsiteEvaluating the Incidence of Opioid-Induced Respiratory Depression Associated with Oliceridine and Morphine as Measured by the Frequency and Average Cumulative Duration of Dosing Interruption in Patients Treated for Acute Postoperative Pain.
Sabry Ayad, Mark A. Demitrack, David A. Burt, Cathy Michalsky, Linda Wase, Michael J. Fossler & Ashish K. Khanna. Clin Drug Investig (2020).
View WebsiteOliceridine, a G protein-selective ligand at the μ-opioid receptor, for the management of moderate to severe acute pain
Gan TJ & Wase L. Drugs Today (Barc). 2020 Apr;56(4):269-286. doi: 10.1358/dot.2020.56.4.3107707.
View PDFPhase 3 “Real World” Safety Study for Oliceridine
ATHENA: A Phase 3, Open-Label Study Of The Safety And Effectiveness Of Oliceridine (TRV130), A G-Protein Selective Agonist At The μ-Opioid Receptor, In Patients With Moderate To Severe Acute Pain Requiring Parenteral Opioid Therapy
Bergese SD, Brzezinski M, Hammer GB, Beard TL, Pan PH, Mace SE, Berkowitz RD, Cochrane K, Wase L, Minkowitz HS, Habib AS. J Pain Research. 2019, 12: 3113-3126.
DOI: 10.2147/JPR.S217563 [open access]
Pharmacokinetics of IV oliceridine in patients with renal impairment or patients with mild/moderate hepatic impairment- No dose adjustments required
The Influence of Renal or Hepatic Impairment on the Pharmacokinetics, Safety, and Tolerability of Oliceridine
Nafziger AN, Arscott KA, Cochrane K, Skobieranda F, Burt DA, Fossler MJ. Clin Pharmacol Drug Dev. 2019 Nov 7. doi:10.1002/cpdd.750.[open access]
Oliceridine (TRV130) Phase-3 Pivotal trial in soft-tissue (abdominoplasty) acute pain
APOLLO-2: A Randomized, Placebo and Active-Controlled Phase III Study Investigating Oliceridine (TRV130), a G Protein-Biased Ligand at the μ-Opioid Receptor, for Management of Moderate to Severe Acute Pain Following Abdominoplasty
Neil K. Singla, Franck Skobieranda, David G. Soergel, Monica Salamea, David A. Burt, Mark A. Demitrack, Eugene R. Viscusi Pain Pract. 2019 Sep;19(7):715-731
Oliceridine (TRV130) Phase-3 Pivotal trial in hard-tissue (bunionectomy) acute pain
APOLLO-1: a randomized placebo and active-controlled phase III study investigating oliceridine (TRV130), a G protein-biased ligand at the µ-opioid receptor, for management of moderate-to-severe acute pain following bunionectomy
Eugene R Viscusi, Franck Skobieranda, David G Soergel,Emily Cook, David A Burt, and Neil Singla. J Pain Res. 2019; 12: 927–943.
Oliceridine (TRV130) Phase 2b trial in soft-tissue (abdominoplasty) acute pain
A randomized, Phase IIb study investigating oliceridine (TRV130), a novel µ-receptor G-protein pathway selective (μ-GPS) modulator, for the management of moderate to severe acute pain following abdominoplasty
Neil Singla, Harold S Minkowitz, David G Soergel, David A Burt, Ruth Ann Subach, Monica Y Salamea, Michael J Fossler, and Franck Skobieranda. J Pain Res. 2017; 10: 2413–2424
View WebsiteOliceridine (TRV130) Phase 2 trial in hard-tissue (bunionectomy) acute pain
A randomized, phase 2 study investigating TRV130, a biased ligand of the μ-opioid receptor, for the intravenous treatment of acute pain.
Viscusi ER, Webster L, Kuss M, Daniels S, Bolognese JA, Zuckerman S, Soergel DG, Subach RA, Cook E, Skobieranda F. Pain. 2016 Jan;157(1):264-72.
TRV130 – analgesia and ventilatory response to hypercapnia vs. morphine in healthy volunteers
Biased agonism of the μ-opioid receptor by TRV130 increases analgesia and reduces on-target adverse effects versus morphine: A randomized, double-blind, placebo-controlled, crossover study in healthy volunteers
Soergel DG, Subach RA, Burnham N, et al. Pain. 2014;155(9):1829-1835. doi:10.1016/j.pain.2014.06.011
View WebsiteTRV130- First clinical experience, pharmacokinetics and pharmacodynamics
First clinical experience with TRV130: pharmacokinetics and pharmacodynamics in healthy volunteers
Soergel DG, Subach RA, Sadler B, Connell J, Marion AS, Cowan CL, Violin JD, Lark MW. J Clin Pharmacol. 2014 Mar;54(3):351-7.
View WebsiteTRV130-Concept of biased ligand
Structure-activity relationships and discovery of a G protein biased μ opioid receptor ligand, [(3-methoxythiophen-2-yl)methyl]({2-[(9R)-9-(pyridin-2-yl)-6-oxaspiro-[4.5]decan-9-yl]ethyl})amine (TRV130), for the treatment of acute severe pain
Chen XT, Pitis P, Liu G, Yuan C, Gotchev D, Cowan CL, Rominger DH, Koblish M, Dewire SM, Crombie AL, Violin JD, Yamashita DS. J Med Chem. 2013 Oct 24;56(20):8019-31.
View WebsiteTRV-130 preclinical safety results
A G protein-biased ligand at the μ-opioid receptor is potently analgesic with reduced gastrointestinal and respiratory dysfunction compared with morphine
DeWire SM, Yamashita DS, Rominger DH, Liu G, Cowan CL, Graczyk TM, Chen XT, Pitis PM, Gotchev D, Yuan C, Koblish M, Lark MW, Violin JD. J Pharmacol Exp Ther. 2013 Mar;344(3):708-17.
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