Thursday Jun 13 | CiteULike
A randomized phase II study to evaluate tacrolimus in combination...
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Micell Technologies Receives CE Mark Approval for MiStent SES
The MiStent SES is unique in providing local drug delivery both during and after the period of polymer absorption, thereby eliminating long-term polymer exposure, a potential cause of delayed healing and late adverse events.
Epstein-Barr virus-associated smooth muscle tumors after kidney...
BACKGROUND: Epstein-Barr virus-associated smooth muscle tumors in adult kidney transplant recipients are rare.
Market Report, "Cappella Inc. - Medical Equipment - Deals and Alliances Profile", published
It develops and provides novel solutions for the treatment of complex coronary artery disease.
Sunlight linked to drug's effectiveness
ISLAMABAD: A new study has demonstrated that the body's ability to break down medicines may be closely related to exposure to sunlight, and thus may vary with the seasons.
OrbusNeich Launches World's First Dual Therapy Stent That...
The introduction of the COMBO Stent is in conjunction with the company's receipt of a CE Mark for the product and involves a sales roll-out in The COMBO Dual Therapy Stent is the first stent to both accelerate endothelial coverage and control neo-intimal proliferation through the combination of OrbusNeich's proven pro-healing technology with an ... (more)
Bioresorbable Drug-Eluting Scaffolds Emerging As The Dominant...
Main Category: Heart Disease Also Included In: Cardiovascular / Cardiology ; Medical Devices / Diagnostics Article Date: 24 May 2013 - 1:00 PDT The DESolve bioresorbable coronary scaffold system achieves good efficacy and safety with low rates of late lumen loss and major coronary adverse events at six months, show first results from the pivotal ... (more)
Results Of The BIOFLOW-II Substudy: Biodegradable Stent Proves Non-Inferior To Drug-Eluting Stent
The Orsiro stent, which is a novel stent platform eluting sirolimus from a biodegradable polymer, demonstrated non-inferiority to the Xience Prime everolimus-eluting stent for the primary angiographic endpoint of in-stent late lumen loss at nine months in the results of an imaging substudy reported at EuroPCR 2013 today.
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Svelte Drug-Eluting Stent Utilizing New Class of Bioabsorbable Drug...
Final 6 and 12-month results of the DIRECT first-in-man clinical study were presented by study principal investigator Dr.
Biodegradable stent proves non-inferior to drug-eluting stent
The BIOFLOW-II substudy used intravascular ultrasound and optical coherence tomography to quantitatively assess neointimal hyperplasia and stent apposition at nine months after treating patients with symptomatic coronary artery disease due to de novo stenotic lesions.