Anaconda Biomed are developing next-generation thrombectomy systems. They have announced a conditional IDE approval from the U.S. FDA to begin the ATHENA study of its ANA Funnel Catheter.
This prospective, randomized, multi-center study will assess the safety and effectiveness of the ANA Funnel Catheter in combination with a stent retriever for mechanical #thrombectomy.
“The IDE approval marks an exciting milestone in our company’s mission to deliver new, safe, and effective solutions that can meaningfully improve the treatment of stroke,” said Anaconda Biomed CEO Francois Salmon.
Dr.Adnan Siddiqui, MD, PhD, coordinating investigator of the ATHENA study, added, “The neurointerventional community is eager to assess this innovative technology, which is designed to enhance the efficiency of mechanical thrombectomy. Even a small difference in revascularization success after one pass can have a profound impact on the clinical outcomes of people with ischemic stroke.”
Studies indicate that flow arrest during mechanical thrombectomy can improve revascularization rates and clinical outcomes. However, this approach has been underutilized due to current device limitations.
Anaconda Biomed’s ANA Funnel Catheter is uniquely designed to facilitate flow arrest during clot retrieval.
Upon IRB approval, the ATHENA study will be conducted at up to 40 U.S. and international centers, enrolling patients with acute #ischemic stroke treated within 24 hours of symptom onset. The study will report acute reperfusion success after a single thrombectomy pass and procedural safety between study arms.
Congratulations to Francois, Ofir Arad, David Harari, Hendrik Lambert and the wider Anaconda BioMed team!
#neurointerventional #idestudy #neurovascular #stroke