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Penumbra, Inc. Announces Completion of THUNDER IDE Study Enrollment for Acute Ischemic Stroke Penumbra, Inc. (NYSE: PEN), the world's leading thrombectomy company, announced the completion of enrollment in its THUNDER clinical study for...

Key Takeaway: Penumbra, Inc. has announced the completion of enrollment in the THUNDER clinical study aimed at evaluating its innovative Thunderbolt technology for treating acute ischemic stroke. This study includes patients with intracranial large vessel occlusion who are eligible for mechanical thrombectomy. The primary endpoint focuses on the effectiveness of revascularization immediately following the procedure. The company emphasizes that this advancement is a crucial step in enhancing stroke management and improving patient outcomes.

Market Sentiment Analysis

POSITIVE FACTORS

  • Completion of enrollment in the THUNDER study marks a significant milestone.
  • Potential to revolutionize stroke management with the Thunderbolt technology.
  • Utilization of advanced CAVT technology may improve patient outcomes.

CONCERNS & RISKS

  • Forward-looking statements carry risks and uncertainties that could impact actual results.
  • Potential adverse outcomes in future clinical trials remain a concern.
  • Competition and market introduction challenges could affect product success.

Full Press Release Details

ALAMEDA, Calif. , Oct. 14, 2024 /PRNewswire/ -- Penumbra, Inc . (NYSE: PEN ), the world's leading thrombectomy company, announced the completion of enrollment in its THUNDER clinical study for patients with acute ischemic stroke. THUNDER is evaluating the safety and efficacy of the company's latest computer assisted vacuum thrombectomy (CAVT™) technology, Penumbra System™ with Thunderbolt™ Aspiration Tubing, for the removal of blood clots in the brain.
"This critical milestone brings us another step closer to providing physicians with the latest technology for stroke management," said Adam Elsesser , president and chief executive officer of Penumbra. "The THUNDER study will provide the data set needed to evaluate Penumbra's Thunderbolt technology and I am optimistic that we are at the dawn of a new era in stroke treatment."
Penumbra System with Thunderbolt Aspiration Tubing uses an advanced CAVT software algorithm to generate proprietary modulated aspiration, reducing friction between the clot and reperfusion catheter and facilitating a more rapid and complete removal of blood clots in the brain. Thunderbolt Aspiration Tubing has been designed for use with Penumbra ENGINE™ and RED™ reperfusion catheter s.
The THUNDER study ( NCT05437055 ) is a multi-center, single-arm study evaluating patients with acute ischemic stroke secondary to intracranial large vessel occlusion (LVO) who are eligible for mechanical thrombectomy. The primary efficacy endpoint includes revascularization of the occluded target vessel at immediate post-procedure.
About Penumbra Penumbra Inc., the world's leading thrombectomy company, is focused on developing the most innovative technologies for challenging medical conditions such as ischemic stroke, venous thromboembolism such as pulmonary embolism, and acute limb ischemia. Its broad portfolio, which includes computer assisted vacuum thrombectomy (CAVT), centers on removing blood clots from head-to-toe with speed, safety and simplicity. By pioneering these innovations, Penumbra supports healthcare providers, hospitals and clinics in more than 100 countries, working to improve patient outcomes and quality of life. For more information, visit www.penumbrainc.com and connect on Instagram , LinkedIn and X .
Important Safety Information Additional information about Penumbra's products can be located on Penumbra's website at https://www.penumbrainc.com/providers . Prior to use, please refer to Instructions for Use for complete product indications, contraindications, warnings, precautions, potential adverse events and detailed instructions for use. Risk information can be found at http://www.peninc.info/risk .
Forward-Looking Statements Except for historical information, certain statements in this press release are forward-looking in nature and are subject to risks, uncertainties and assumptions about us. Our business and operations are subject to a variety of risks and uncertainties and, consequently, actual results may differ materially from those projected by any forward-looking statements. Factors that could cause actual results to differ from those projected include, but are not limited to: failure to sustain or grow profitability or generate positive cash flows; failure to effectively introduce and market new products; delays in product introductions; significant competition; inability to further penetrate our current customer base, expand our user base and increase the frequency of use of our products by our customers; inability to achieve or maintain satisfactory pricing and margins; manufacturing difficulties; permanent write-downs or write-offs of our inventory or other assets; product defects or failures; unfavorable outcomes in clinical trials; inability to maintain our culture as we grow; fluctuations in foreign currency exchange rates; potential adverse regulatory actions; and the potential impact of any acquisitions, mergers, dispositions, joint ventures or investments we may make. These risks and uncertainties, as well as others, are discussed in greater detail in our filings with the Securities and Exchange Commission (SEC), including our Annual Report on Form 10-K for the year ended December 31, 2023 filed with the SEC on February 22, 2024 . There may be additional risks of which we are not presently aware or that we currently believe are immaterial which could have an adverse impact on our business. Any forward-looking statements are based on our current expectations, estimates and assumptions regarding future events and are applicable only as of the dates of such statements. We make no commitment to revise or update any forward-looking statements in order to reflect events or circumstances that may change.
Contact
Jennifer Heth Parinaz Farzin
Penumbra, Inc. Merryman Communications
[email protected] [email protected]
510-995-9791 310.600.6746
SOURCE Penumbra, Inc.

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Frequently Asked Questions

What is the THUNDER clinical study?

The THUNDER study evaluates Penumbra's CAVT technology for treating acute ischemic stroke.

What technology is being tested in the THUNDER study?

The study tests the Penumbra System with Thunderbolt Aspiration Tubing.

What is the primary endpoint of the THUNDER study?

The primary efficacy endpoint is revascularization of the occluded target vessel post-procedure.

What types of patients are included in the THUNDER study?

Patients with acute ischemic stroke due to large vessel occlusion are included.

Who leads Penumbra, Inc.?

Adam Elsesser is the president and CEO of Penumbra, Inc.

Last updated: Oct 14, 2024