M onotherapy drug-eluting stents (DES) suppress neointimal proliferation and reduce the 1-year target lesion revascularization rate better than bare-metal stents but have other issues about safety and efficacy.1,2 Inadequate endothelial strut coverage causes stent thrombosis requiring stringent dual-antiplatelet therapy. 3,4 Late catch-up with cumulative increase in the target lesion revascularization rate seems inevitable for most monotherapy DES.5 AcceleratedBackground-Current monotherapy drug-eluting stents are associated with impaired healing, neoatherosclerosis, and late stent thrombosis. The healing profile and neointimal transformation of the first dual-therapy endothelial progenitor cellcapturing sirolimus-eluting stent are unknown. Methods and Results-In this prospective, single-center study, 61 patients treated with the Combo stent had optical coherence tomography at baseline, early follow-up (4 monthly groups in a 1:2:2:1 ratio from 2 to 5 months), 9 months, and 24 months. Optical coherence tomography early strut coverage increased from 77.1% to 92.5% to 92.7% to 94.9% between 2 and 5 months. At 9 months, the major adverse cardiac event rate was 1.64%, and angiographic in-stent late loss was 0.24 mm (0.08-0.40). The 36-month major adverse cardiac event rate was 3.3%. From 9 to 24 months, neointimal regression was confirmed by optical coherence tomography: neointimal thickness (median [first quartile and third quartile]), 0.14 mm (0.08 and 0. Conclusions-With additional endothelial progenitor cell-capturing technology, the Combo stent exhibits a unique late neointimal regression (from 9 to 24 months) that has not been reported in any drug-eluting stents, translating into good 36-month clinical results with minimal restenosis and no late stent thrombosis. This is the first study testing the concept of using a longitudinal sequential optical coherence tomography protocol to continuously document early healing profile and late neointimal transformation, predicting long-term outcomes of a new novel stent platform. Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifiers: NCT01274234, NCT01756807, and NCT02263313. Technology to capture endothelial progenitor cells with an anti-CD34 antibody coating has been developed as a radically different approach to promote vessel healing. [8][9][10] This technology has been combined with an abluminal sirolimus-eluting coating composed of a biodegradable polymer to form a new DES platform, the Combo stent (OrbusNeich Medical, Fort Lauderdale, FL). Sirolimus release (5 µg/mm) is completed in 30 days, and the biodegradable polymer disappears within 90 days. This dualtherapy approach aims for neointimal suppression while retaining the endothelial progenitor cell-capturing prohealing benefits enabling rapid endothelialization. [11][12][13] We have used a vigorous imaging protocol (longitudinal sequential optical coherence tomography [OCT] assessments) to evaluate this new Combo platform by monitoring its healing profile and neointimal transformati...