TY - JOUR
T1 - Final Results of the RHAPSODY Trial
T2 - A Multi-Center, Phase 2 Trial Using a Continual Reassessment Method to Determine the Safety and Tolerability of 3K3A-APC, A Recombinant Variant of Human Activated Protein C, in Combination with Tissue Plasminogen Activator, Mechanical Thrombectomy or both in Moderate to Severe Acute Ischemic Stroke
AU - the NeuroNEXT Clinical Trials Network NN104 Investigators
AU - Lyden, Patrick
AU - Pryor, Kent E.
AU - Coffey, Christopher S.
AU - Cudkowicz, Merit
AU - Conwit, Robin
AU - Jadhav, Ashutosh
AU - Sawyer, Robert N.
AU - Claassen, Jan
AU - Adeoye, Opeolu
AU - Song, Shlee
AU - Hannon, Peter
AU - Rost, Natalia S.
AU - Hinduja, Archana
AU - Torbey, Michel
AU - Lee, Jin Moo
AU - Benesch, Curtis
AU - Rippee, Michael
AU - Rymer, Marilyn
AU - Froehler, Michael T.
AU - Clarke Haley, E.
AU - Johnson, Mark
AU - Yankey, Jon
AU - Magee, Kim
AU - Qidwai, Julie
AU - Levy, Howard
AU - Mark Haacke, E.
AU - Fawaz, Miller
AU - Davis, Thomas P.
AU - Toga, Arthur W.
AU - Griffin, John H.
AU - Zlokovic, Berislav V.
N1 - Funding Information:
This trial was funded by the National Institute of Neurological Disorders and Stroke (NINDS; U01NS088312). The NeuroNEXT Network is supported by the National Institute of Neurological Disorders and Stroke (Clinical Coordinating Center: U01NS077179; Data Coordinating Center: U01NS077352). Research reported in this publication was also supported by the National Center for Advancing Translational Sciences of the National Institutes of Health under award numbers of Columbia University Medical Center (UL1TR000040), University at Buffalo/ SUNY (UL1TR001412), Vanderbilt University (ULTR002243), and Washington University at St. Louis (UL1TR000448). Its contents are solely the responsibility of the authors and do not necessarily represent official views of the National Center for Advancing Translational Sciences or the National Institutes of Health. This clinical trial was approved by the NeuroNEXT Executive Committee (Co-Chairs: Christopher Coffey, PhD, and Merit Cudkowicz, MD, MSc). The NINDS NeuroNEXT Data and Safety Monitoring Board and Independent Medical Monitors (Harold Adams, MD, Enrique Leira, MD, and Cheryl Bushnell, MD) provided safety and trial oversight. We acknowledge the expertise and guidance of the following: Dixie Ecklund, Marianne Chase, Steven Greenberg, MD, PhD, Mark P. Goldberg, MD, Sara Weymer, Frank del Greco, Pooja Khanolkar, MPH, and Samantha King; the Partners Human Research Affairs for coordination and implementation of the single IRB model.
Funding Information:
This trial was funded by the National Institute of Neurological Disorders and Stroke (NINDS; U01NS088312). The NeuroNEXT Network is supported by the National Institute of Neurological Disorders and Stroke (Clinical Coordinating Center: U01NS077179; Data Coordinating Center: U01NS077352). Research reported in this publication was also supported by the National Center for Advancing Translational Sciences of the National Institutes of Health under award numbers of Columbia University Medical Center (UL1TR000040), University at Buffalo/ SUNY (UL1TR001412), Vanderbilt University (ULTR002243), and Washington University at St. Louis (UL1TR000448). Its contents are solely the responsibility of the authors and do not necessarily represent official views of the National Center for Advancing Translational Sciences or the National Institutes of Health. This clinical trial was approved by the NeuroNEXT Executive Committee (CoChairs: Christopher Coffey, PhD, and Merit Cudkowicz, MD, MSc). The NINDS NeuroNEXT Data and Safety Monitoring Board and Independent Medical Monitors (Harold Adams, MD, Enrique Leira, MD, and Cheryl Bushnell, MD) provided safety and trial oversight.
Publisher Copyright:
© 2018 American Neurological Association
PY - 2019/1
Y1 - 2019/1
N2 - Objective: Agonism of protease-activated receptor (PAR) 1 by activated protein C (APC) provides neuro- and vasculoprotection in experimental neuroinjury models. The pleiotropic PAR1 agonist, 3K3A-APC, reduces neurological injury and promotes vascular integrity; 3K3A-APC proved safe in human volunteers. We performed a randomized, controlled, blinded trial to determine the maximally tolerated dose (MTD) of 3K3A-APC in ischemic stroke patients. Methods: The NeuroNEXT trial, RHAPSODY, used a novel continual reassessment method to determine the MTD using tiers of 120, 240, 360, and 540 μg/kg of 3K3A-APC. After intravenous tissue plasminogen activator, intra-arterial mechanical thrombectomy, or both, patients were randomized to 1 of the 4 doses or placebo. Vasculoprotection was assessed as microbleed and intracranial hemorrhage (ICH) rates. Results: Between January 2015 and July 2017, we treated 110 patients. Demographics resembled a typical stroke population. The MTD was the highest-dose 3K3A-APC tested, 540 μg/kg, with an estimated toxicity rate of 7%. There was no difference in prespecified ICH rates. In exploratory analyses, 3K3A-APC reduced ICH rates compared to placebo from 86.5% to 67.4% in the combined treatment arms (p = 0.046) and total hemorrhage volume from an average of 2.1 ± 5.8 ml in placebo to 0.8 ± 2.1 ml in the combined treatment arms (p = 0.066). Interpretation: RHAPSODY is the first trial of a neuroprotectant for acute ischemic stroke in a trial design allowing thrombectomy, thrombolysis, or both. The MTD was 540 μg/kg for the PAR1 active cytoprotectant, 3K3A-APC. A trend toward lower hemorrhage rate in an exploratory analysis requires confirmation. Clinical Trial Registration: Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT02222714. ANN NEUROL 2019;85:125–136.
AB - Objective: Agonism of protease-activated receptor (PAR) 1 by activated protein C (APC) provides neuro- and vasculoprotection in experimental neuroinjury models. The pleiotropic PAR1 agonist, 3K3A-APC, reduces neurological injury and promotes vascular integrity; 3K3A-APC proved safe in human volunteers. We performed a randomized, controlled, blinded trial to determine the maximally tolerated dose (MTD) of 3K3A-APC in ischemic stroke patients. Methods: The NeuroNEXT trial, RHAPSODY, used a novel continual reassessment method to determine the MTD using tiers of 120, 240, 360, and 540 μg/kg of 3K3A-APC. After intravenous tissue plasminogen activator, intra-arterial mechanical thrombectomy, or both, patients were randomized to 1 of the 4 doses or placebo. Vasculoprotection was assessed as microbleed and intracranial hemorrhage (ICH) rates. Results: Between January 2015 and July 2017, we treated 110 patients. Demographics resembled a typical stroke population. The MTD was the highest-dose 3K3A-APC tested, 540 μg/kg, with an estimated toxicity rate of 7%. There was no difference in prespecified ICH rates. In exploratory analyses, 3K3A-APC reduced ICH rates compared to placebo from 86.5% to 67.4% in the combined treatment arms (p = 0.046) and total hemorrhage volume from an average of 2.1 ± 5.8 ml in placebo to 0.8 ± 2.1 ml in the combined treatment arms (p = 0.066). Interpretation: RHAPSODY is the first trial of a neuroprotectant for acute ischemic stroke in a trial design allowing thrombectomy, thrombolysis, or both. The MTD was 540 μg/kg for the PAR1 active cytoprotectant, 3K3A-APC. A trend toward lower hemorrhage rate in an exploratory analysis requires confirmation. Clinical Trial Registration: Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT02222714. ANN NEUROL 2019;85:125–136.
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U2 - 10.1002/ana.25383
DO - 10.1002/ana.25383
M3 - Article
C2 - 30450637
AN - SCOPUS:85059588487
SN - 0364-5134
VL - 85
SP - 125
EP - 136
JO - Annals of Neurology
JF - Annals of Neurology
IS - 1
ER -