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For all cataract surgeons managing glaucoma patients

The world’s first, IOL-mounted, controlled release drug delivery platform capable of delivering multiple years of therapy

CONSISTENT DAILY RELEASE

Targeting 3-year delivery of bimatoprost to treat glaucoma in patients undergoing cataract surgery

Dual pads securely attached to each haptic are designed to elute treatment continuously for multiple years. 

The SpyGlass Pharma™ Drug Delivery Platform has not been approved by the FDA

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Directly addressing an unmet need

Patient non-adherence to their glaucoma medication can lead to complications, disease progression and vision loss. Methods of drug delivery independent of patient behavior is an industry-wide need.

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Millions of glaucoma patients undergo cataract surgery each year

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INNOVATIVE PLATFORM

Explore the pioneering technology behind the SpyGlass Pharma™ Drug Delivery Platform

VERSATILE PLATFORM

Designed to deliver multiple drugs to address additional ophthalmic indications

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The device you know coupled with treatment you trust. All within the same procedure you know by heart.

The SpyGlass Pharma™ Drug Delivery Platform is Implanted with the IOL into the capsular bag using surgical techniques identical to standard cataract procedures. 

Intraocular drug delivery that lasts

Learn more about SpyGlass Pharma™ 

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SpyGlass Pharma Announces Positive 36-Month First-in-Human and 3-Month Phase I/II Trial Results for Its Novel BIM-IOL System

ALISO VIEJO, Calif., Nov. 10, 2025 (GLOBE NEWSWIRE) --  SpyGlass Pharma™, a late-stage biopharmaceutical company, announces positive results from two clinical trials of its lead product candidate, the Bimatoprost Drug Pad-IOL System (BIM-IOL System), for the treatment of elevated IOP in patients with mild-to-moderate open-angle glaucoma (OAG) or ocular hypertension (OHT). The data were presented by Malik Kahook, M.D., co-founder and president of SpyGlass Pharma, at the Interventional Glaucoma Consortium (IGC) in Salt Lake City, Utah on Saturday, November 8th, which included 36-month follow-up data from the FIH trial and three-month interim safety and efficacy results from the Phase I/II trial. (View full press release)

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Tel: 949-284-6904

27061 Aliso Creek Rd, Suite 100
Aliso Viejo, CA 92656

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