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Ceretrieve Announces Groundbreaking Success in FIH Ischemic Stroke Cases

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Ceretrieve announced successful results of its multicenter, single-arm study for its aspiration catheter, aimed at treating acute ischemic stroke (AIS) caused by large vessel occlusion (LVO).

The study involved 20 patients and achieved 100% Complete/Near-Complete Perfusion with the Gen 2 device, far exceeding the 30%-40% rate of current gold-standard devices.

Ceretrieve's device allows single-pass clot removal and full blood flow restoration, ensuring high safety by minimizing the risk of clot fragments moving further into the brain.

The technology demonstrated superior performance compared to existing devices, highlighting its potential to significantly improve post-stroke patient outcomes.

Positive
  • 100% Complete/Near-Complete Perfusion achieved with Gen 2 device.
  • 83% First Pass Complete Perfusion, exceeding current gold-standard rates of 30%-40%.
  • Single-pass clot removal and full blood flow restoration.
  • High safety standards, reducing the risk of clot fragments moving further into the brain.
  • Superior performance compared to existing devices.
  • Potential to significantly improve post-stroke patient outcomes.
Negative
  • Study sample size was to 20 patients.
  • Results are preliminary and based on a single-arm study without a control group for comparison.

Ceretrieve's aspiration catheter demonstrated clots removal, completely restoring blood flow in a single pass.

YOKNEAM, Israel, May 28, 2024 /PRNewswire/ -- Ceretrieve announced today the successful results of the company's multicenter, single-arm study, showcasing the capabilities of its state-of-the-art aspiration catheter. The study, conducted across two centers, included 20 patients who suffered from acute ischemic stroke (AIS) due to intracranial large vessel occlusion (LVO) and were eligible for thrombectomy within 24 hours of symptom onset. The study was aimed for assessing the safety and initial performance of the Ceretrieve Device.

Redefining Stroke Treatment

Ceretrieve's mission is to transform stroke care, save lives, minimize disability, and significantly improve post-stroke quality of life. Ceretrieve's aspiration catheter is at the forefront of this mission, delivering aspiration capabilities that are far superior when compared to existing devices, allowing clot(s) removal in a single pass, while fully restoring blood flow. Designed for seamless integration within a conventional 6Fr delivery catheter, Ceretrieve's device offers exceptional trackability and maneuverability, ensuring efficient access to the clot location.

As shown in the study conducted, Ceretrieve's aspiration catheter not only excelled in performance but also ensured the highest safety standards by reducing the risk of releasing clot fragments further into the brain. In the first-in-human (FIH) study 80% Complete/Near-Complete Perfusion was achieved.

The study included two generations of the device, and the results with the improved Gen 2 device are highly impressive: 100% Complete/Near-Complete Perfusion achieved in all treated patients; and 83% First Pass Complete Perfusion (FPE mTICI 3), far exceeding the 30%-40% rate of current gold-standard devices.

Ceretrieve's CEO, Maysa Mustafa: "The promising results of our clinical studies are the culmination of years of hard work and R&D. Our mission to redefine stroke treatment drives everything we do, and these results signify a major leap forward in saving and dramatically improving lives following an ischemic stroke."

"The 'first pass effect' has been shown to improve patient outcomes" says Dr. Shady Jashan (Galilee Medical Center, Israel) who performed the first neuro thrombectomy procedure with the Ceretrieve device. "Our experience in FIH trials demonstrated that the Ceretrieve device quickly enables complete clot ingestion in first pass even for the most challenging clots and anatomies. This has the potential to dramatically improve patient clinical outcomes."

Prof. Serder Geyik, MD (Florya Medical Park, Turkey): "The term 'Everything comes with a price' is not valid for the Ceretrieve device. Ceretrieve's device aspirates the clot with a giant bore tip- double than the largest catheters in the market, for maximal vacuum effect without paying the price in trackability. In addition, it provides local flow restriction in the middle cerebral artery reducing distal emboli. It is the only device that includes all the features for successful thrombectomy and first pass effect in one single device. "

Amir Belson, M.D., Ceretrieve Chair: "With Ceretrieve's advanced technology, we are seeing significant improvements in patient recovery rates. This innovation is setting a new standard in stroke care, offering patients better outcomes and real hope for recovery."

About Ceretrieve

Ceretrieve's vision is to be the doctor's first-choice device in treating ischemic stroke offering complete treatment with superior performance in one device. Ceretrieve was established in 2017 in collaboration with The Trendlines Group (SGX:42T) (OTCQX: TRNLY), a leading investment group based in Israel and Singapore, as well as the Israel Innovation Authority (IIA) Incubators Program. Agriline and several angel investors are among the Company's additional investors.

Contact:
Maysa Mustafa, CEO
maysa@ceretrieve.com

Photo - https://mma.prnewswire.com/media/2423407/Ceretrieve_case.jpg

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SOURCE Ceretrieve

FAQ

What were the results of Ceretrieve's study for its aspiration catheter?

The study achieved 100% Complete/Near-Complete Perfusion with the Gen 2 device and 83% First Pass Complete Perfusion.

How effective is Ceretrieve's aspiration catheter in removing clots?

Ceretrieve's aspiration catheter removes clots in a single pass, fully restoring blood flow and ensuring high safety.

What is the significance of the first pass effect for Ceretrieve's device?

The first pass effect, with an 83% success rate, dramatically improves patient outcomes by enabling complete clot ingestion in a single pass.

How does Ceretrieve's device compare to current gold-standard devices?

Ceretrieve's device far exceeds current gold-standard devices with a 100% Complete/Near-Complete Perfusion rate compared to 30%-40%.

What safety measures does Ceretrieve's aspiration catheter offer?

The device minimizes the risk of clot fragments moving further into the brain, ensuring high safety standards.

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