Stellarex drug-coated balloon (DCB), featuring EnduraCoat technology, provides top-tier patency to treat common-to-complex lesions with a low drug dose. Low clinically driven target lesion revascularization rates demonstrate the safety of Stellarex across all patients.
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Effective low drug dose matters
Effective low drug dose matters
Dose excess and particulate downstream possibly results in a delay of wound healing, loss of microcirculation and creation of aneurysms¹⁰⁻¹³. Stellarex is the only low dose DCB with a statistically significant treatment effect in femoropopliteal lesions².
Effective low drug dose matters
Dose excess and particulate downstream possibly results in a delay of wound healing, loss of microcirculation and creation of aneurysms¹⁰⁻¹³. Stellarex is the only low dose DCB with a statistically significant treatment effect in femoropopliteal lesions².
Effective low drug dose matters
Dose excess and particulate downstream possibly results in a delay of wound healing, loss of microcirculation and creation of aneurysms¹⁰⁻¹³. Stellarex is the only low dose DCB with a statistically significant treatment effect in femoropopliteal lesions².
Dose excess and particulate downstream possibly results in a delay of wound healing, loss of microcirculation and creation of aneurysms¹⁰⁻¹³. Stellarex is the only low dose DCB with a statistically significant treatment effect in femoropopliteal lesions².
Proven performance in calcium
Proven performance in calcium
PEG forms strong ionic bonds with hydroxyl apatite (HAp), the primary component of calcified atherosclerotic lesions¹⁴. PEG’s affinity for HAp may result in limited PTX washout in the presence of calcium.
Proven performance in calcium
PEG forms strong ionic bonds with hydroxyl apatite (HAp), the primary component of calcified atherosclerotic lesions¹⁴. PEG’s affinity for HAp may result in limited PTX washout in the presence of calcium.
Proven performance in calcium
PEG forms strong ionic bonds with hydroxyl apatite (HAp), the primary component of calcified atherosclerotic lesions¹⁴. PEG’s affinity for HAp may result in limited PTX washout in the presence of calcium.
PEG forms strong ionic bonds with hydroxyl apatite (HAp), the primary component of calcified atherosclerotic lesions¹⁴. PEG’s affinity for HAp may result in limited PTX washout in the presence of calcium.
Sustained tissue Residency
Sustained tissue Residency
Hybrid paclitaxel offers prompt drug transfer and sustained tissue residency through 28 day restenotic window¹⁵⁻¹⁶.
Sustained tissue Residency
Hybrid paclitaxel offers prompt drug transfer and sustained tissue residency through 28 day restenotic window¹⁵⁻¹⁶.
Sustained tissue Residency
Hybrid paclitaxel offers prompt drug transfer and sustained tissue residency through 28 day restenotic window¹⁵⁻¹⁶.
Dose excess and particulate downstream possibly results in a delay of wound healing, loss of microcirculation and creation of aneurysms¹⁰⁻¹³. Stellarex is the only low dose DCB with a statistically significant treatment effect in femoropopliteal lesions².
Effective low drug dose matters
Dose excess and particulate downstream possibly results in a delay of wound healing, loss of microcirculation and creation of aneurysms¹⁰⁻¹³. Stellarex is the only low dose DCB with a statistically significant treatment effect in femoropopliteal lesions².
Effective low drug dose matters
Dose excess and particulate downstream possibly results in a delay of wound healing, loss of microcirculation and creation of aneurysms¹⁰⁻¹³. Stellarex is the only low dose DCB with a statistically significant treatment effect in femoropopliteal lesions².
Dose excess and particulate downstream possibly results in a delay of wound healing, loss of microcirculation and creation of aneurysms¹⁰⁻¹³. Stellarex is the only low dose DCB with a statistically significant treatment effect in femoropopliteal lesions².
Proven performance in calcium
Proven performance in calcium
PEG forms strong ionic bonds with hydroxyl apatite (HAp), the primary component of calcified atherosclerotic lesions¹⁴. PEG’s affinity for HAp may result in limited PTX washout in the presence of calcium.
Proven performance in calcium
PEG forms strong ionic bonds with hydroxyl apatite (HAp), the primary component of calcified atherosclerotic lesions¹⁴. PEG’s affinity for HAp may result in limited PTX washout in the presence of calcium.
Proven performance in calcium
PEG forms strong ionic bonds with hydroxyl apatite (HAp), the primary component of calcified atherosclerotic lesions¹⁴. PEG’s affinity for HAp may result in limited PTX washout in the presence of calcium.
PEG forms strong ionic bonds with hydroxyl apatite (HAp), the primary component of calcified atherosclerotic lesions¹⁴. PEG’s affinity for HAp may result in limited PTX washout in the presence of calcium.
Sustained tissue Residency
Sustained tissue Residency
Hybrid paclitaxel offers prompt drug transfer and sustained tissue residency through 28 day restenotic window¹⁵⁻¹⁶.
Sustained tissue Residency
Hybrid paclitaxel offers prompt drug transfer and sustained tissue residency through 28 day restenotic window¹⁵⁻¹⁶.
Sustained tissue Residency
Hybrid paclitaxel offers prompt drug transfer and sustained tissue residency through 28 day restenotic window¹⁵⁻¹⁶.
1. Mathews S. NCVH, 2018. ILLUMENATE Pivotal Stellarex DCB IDE Study 2-Year Outcomes. May 30, 2018. New Orleans, LA.
2. Brodmann M. ILLUMENATE EU RCT: 2-year Results; Oral Presentation. VIVA 2017, Las Vegas, NV. September 11-14, 2017.
3. Laird, et al. J Am Coll Cardio. 2015;66:2329-2338. In.Pact Summary of Safety and Effectiveness Data (SSED). Medtronic In.Pact Instructions for Use, M052624T001 Rev 1F.
4. Holden. Comparing Trials Data in the Management of Calcified Arteries. Charing Cross 2018. April 24-26, 2018; London, UK.
5. Zeller. ILLUMENATE Global: 12-month results with the Stellarex DCB in femoropopliteal lesions. LINC. 2017. Leipzig, Germany.
6. Bard Lutonix Instructions for Use, BAW1387400r3.
7. Zeller. ILLUMENATE Global: 2-year results with the Stellarex DCB in femoropopliteal lesions. LINC. 2018. Leipzig, Germany.
8. Stellarex IFU. P011966-D.
9. Lyden S. Oral presentation, TCT 2016, Washington DC. Nov 2, 2016.
10. Data on file. D044595-00.
11. Schroeder H. et al. Circulation 2017;135:2227-2236
12. H. Schroeder et al. Catheter Cardiovasc Interv. 2015.
13. Mark J, et al. Physical properties of polymers. Cambridge University Press. 3rd ed. 2004.
*VasCore (Boston, MA); PSVR: 2.5, KM estimates at day 365 (360 for IN.PACT SFA) Studies shown are not head-to-head comparisons, and data presented cannot be directly compared. Calcium definitions may vary from study to study, and the rates presented here are based on those used and reported in each respective study. Complex patients refers to high rates of severe calcium, diabetes and renal insufficiency estimates. Primary patency based on Kaplan-Meier.
By clicking on the link, you will be leaving the official Royal Philips ("Philips") website. Any links to third-party websites that may appear on this site are provided only for your convenience and in no way represent any affiliation or endorsement of the information provided on those linked websites. Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein.
