Latest Trends In Global drug-coated balloons market

Drug-eluting balloons (DEBs) are being used to treat in-stent restenosis (ISR) instead of drug-eluting stents (DES).

They are covered with a polymeric matrix that contains antiproliferative medicines that are released locally at the vessel wall when the balloon inflates.

DEBs shorten the period of dual antiplatelet medication, remove the danger of stent thrombosis, and allow for more focused drug delivery.

Because of their flexibility in application in complicated lesions, DEBs offer benefits over polymer-related endothelialization and stent distribution.

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Despite showing promise in the treatment of in-stent restenosis, investigations employing drug-coated balloons in de novo coronary lesions have yielded inconsistent outcomes.

The drug-coated balloon in conjunction with a bare-metal stent produced better angiographic outcomes than the bare-metal stent alone, but it did not outperform the DES.

Patients were randomly assigned to either a sirolimus-eluting stent or a combination of a bare-metal stent and drug-coated balloon in the Paclitaxel-Eluting PTCA-Balloon Catheter in Coronary Artery Disease (PEPCAD) III trial.

Not only was in-stent restenosis considerably greater in the drug-coated balloon group, but so were MI, stent thrombosis, and total lesion revascularization at months.

Similarly, during PCI, the -subject Paclitaxel-Coated Balloon Versus Drug-Eluting Stent.

GLOBAL DRUG-COATED BALLOONS MARKET SIZE AND FORECAST

The Global Drug-Coated Balloons Market accounted for $XX Billion in 2022 and is anticipated to reach $XX Billion by 2030, registering a CAGR of XX% from 2023 to 2030.

NEW PRODUCT LAUNCH

Surmodics, Inc., a leading developer of medical device and in vitro diagnostic solutions to the health care sector, announced today that the SurVeil drug-coated balloon (DCB) has received FDA clearance.

The SurVeil DCB is currently available to clinicians in the United States for percutaneous transluminal angioplasty of de novo or restenotic lesions in the femoral and popliteal arteries with reference vessel diameters of mm, following adequate vascular preparation.

In the European Union, the SurVeil DCB obtained CE Mark certification.

Obtaining FDA clearance for SurVeil DCB is one of Surmodics most significant achievements. It is a significant step forward in efforts to create next-generation solutions that will benefit millions of patients suffering from peripheral artery disease.

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SurVeil DCB has exclusive worldwide marketing rights with Abbott. Surmodics will produce and supply the product, earning money from product sales to Abbott as well as a percentage of earnings from Abbott's third-party sales.

Abbott will also pay Surmodics a million dollar milestone bonus. In the third quarter of its fiscal year, the business expects to recognise roughly million in revenue linked to the milestone payment.

Surmodics continues to assist Abbott and its exclusive worldwide commercialization rights for the SurVeil DCB, building on recent accomplishments.

COMPANY PROFILE

Medtronic
PLOS
Frontiers
Boston Scientific
B. Braun

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THIS REPORT WILL ANSWER FOLLOWING QUESTIONS
How many drug-coated balloons are manufactured per annum globally? Who are the sub-component suppliers in different regions?

Cost breakup of a Global drug-coated balloons and key vendor selection criteria

Where are the drug-coated balloons manufactured? What is the average margin per unit?

Market share of Global drug-coated balloons market manufacturers and their upcoming products

Cost advantage for OEMs who manufacture Global drug-coated balloons in-house

key predictions for next 5 years in Global drug-coated balloons market

Average B-2-B drug-coated balloons market price in all segments

Latest trends in drug-coated balloons market, by every market segment

The market size (both volume and value) of the drug-coated balloons market in 2023-2030 and every year in between?

Production breakup of drug-coated balloons market, by suppliers and their OEM relationship

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