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 - 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.
UR - http://www.scopus.com/inward/record.url?scp=85059588487&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85059588487&partnerID=8YFLogxK
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 -