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Ikervis

Manufactured by Santen
Sourced in Japan

Ikervis is a medical device designed for the treatment of dry eye disease. It features an ophthalmic solution that is administered as eye drops.

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4 protocols using ikervis

1

Cataract Surgery Techniques Comparison

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All surgeries were performed by a single, experienced surgeon (HL), employing two surgical techniques: conventional cataract surgery and FLACS (CATALYS™ Precision Laser System, Johnson & Johnson). A hydrophobic 1-piece IOL (Eyhance non-toric, Johnson & Johnson) was implanted, with the lens center aligned with the visual axis. The capsulorhexis center coincided with the lens center and had a size of 5.0 mm. Before the conclusion of every surgery, continuous 360° IOL-capsulorhexis overlap was confirmed. Postoperative topical medications included levofloxacin hydrate 1.5 % (Cravit 1.5 %, Santen Pharmaceutical) four times daily, prednisolone acetate 1.0 % (Predforte 1.0 %, Allergan, Inc.) four times daily, ketorolac tromethamine 0.45 % (Acuvail, Allergan, Inc.) two times daily, and cyclosporin 0.1 % (Ikervis 0.1 %, Santen Pharmaceutical) once daily.
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2

Evaluating MMP-9 Immunoassay Interference in Eye Drops

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To investigate interactions between the MMP-9 immunoassay and components within eye drops, 10 μl of rhMMP-9 (200 ng/ml) was applied to the sample collector, followed by addition of 10 μl of eye drop sample. The following eye drops were used: Elazop (brinzolamide/timolol; Novartis, Basel, Switzerland), Alphagan-P (brimonidine tartrate 0.15%; Allergan, Dublin, Ireland), Isopto Carpine (pilocarpine hydrochloride 2%; Novartis), Bronuck (bromfenac sodium 0.1%; TaeJoon, Seoul, Korea), Cravit (levofloxacin 0.5%; Santen, Tokyo, Japan), Diquas (Diquafosol sodium 3%; Santen), Ikervis (cyclosporine A cationic emulsion 0.1%; Santen, Evry, France), Lotemax (loteprednol etabonate 0.5%; Bausch & Lomb, Rochester, NY, USA), Pazeo (olopatadine hydrochloride 0.7%; Novartis), Lastacaft (alcaftadine 0.25%; Allergan), Mydrin-P (tropicamide 0.5%/phenylephrine 0.5%; Santen), Mydriacyl (tropicamide 1%; Novartis), Cyclogyl (cyclopentolate HCl 1%; Norvatis), Isopto Atropine (atropine hydrochloride 1%; Novartis), and Refresh Tears (carboxymethylcellulose sodium 0.5%; Allergan). The test line was photographed after 10 and 20 min, the density was measured, and the results were compared with a control sample (200 ng/ml of rhMMP-9; 20 μl).
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3

Ciclosporin A and Hydrocortisone Eye Drops

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This study was performed in a randomized, observer-masked design. Both eyes of all patients included in this study were treated with preservative-free ciclosporin A 0.1% eye drops (Ikervis, Santen Pharmaceutical, Osaka, Japan) once daily in the evening for 6 months. One eye of each patient received, additionally, hydrocortisone 0.335% (Softacort, Laboratoires Thea, Clemont-Ferrand, France) eye drops three times daily for the first two weeks of treatment. The eye receiving additional hydrocortisone eye drops was determined by randomization. In addition, all patients included in this study received preservative-free Artelac complete (Bausch & Lomb GmbH, Berlin, Germany) eye drops 5 times per day, containing sodium hyaluronate, carbomer, and medium chain triglycerides.
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4

Prophylaxis for Allo-HSCT Patients

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Participants were prescribed topical cyclosporine-A 0.1% (Ikervis, Santen) prophylaxis once daily to both eyes and preservative-free sodium hyaluronate 0.3% (Hialid Mini, Santen) lubricating eye drop to be used pro re nata (PRN) from 3–5 weeks prior to allo-HSCT to 12 months after allo-HSCT. Depending on the transplant protocol used, participants received systemic GVHD prophylaxis with systemic CsA or tacrolimus therapy combined with a course of methotrexate or mycophenolate. Antithymocyte globulin (ATG) or post-transplant cyclophosphamide was added to the above regime in cases of unrelated/ sibling donor with antigen mismatch or haploidentical transplant, respectively (refer to Supplementary Table 1 for the individualized GVHD prophylaxis regimen used for each patient).
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