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BIM-DRS

Phase 1

Glaucoma | Small molecule | Ophthalmology |SpyGlass Pharma, Inc.|Last Updated: Jun 11, 2026

Target and mechanism

Molecular targetPTGER2
ModalitySmall molecule

Also known as BIM-DRS Low Dose

Success Probability

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Market & Valuation

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Trial Design

CONTROLLED
Total Trials1
Total Enrollment24

FDA Designations

No designations recorded

Clinical trial landscape

BIM-DRS · 1 trial · 2 indications

Phase 1 1
NCT07641296Evaluation of the Safety, Efficacy, Dose Response of the Bimatoprost Drug Ring System (BIM-DRS) in Pseudophakic Patients Diagnosed With Open Angle Glaucoma or Ocular HypertensionGlaucoma
NOT YET_RECRUITING24 Analytics
PHASE1NOT YET_RECRUITING
Evaluation of the Safety, Efficacy, Dose Response of the Bimatoprost Drug Ring System (BIM-DRS) in Pseudophakic Patients Diagnosed With Open Angle Glaucoma or Ocular Hypertension
GlaucomaUnlock trial analytics

Study Endpoints

Primary Endpoints

Mean IOP change from Baseline (mmHg)
Postoperative Week 2, Week 6, and Month 3.

Secondary Endpoints

Mean IOP (mmHg)
Postoperative Week 2, Week 6, and Months 3, 6, 12, 18, 24, 30, and 36
Mean IOP change from Baseline (mmHg)
Postoperative Months 6, 12, 18, 24, 30, and 36
Mean IOP change from Baseline
Postoperative Months 6, 12, 18, 24, 30, and 36
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingSINGLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Bimatoprost-Drug Ring System Low Dose and Previously Implanted Commercially Available Monofocal IOLEXPERIMENTAL -
Bimatoprost-Drug Ring System High Dose and Previously Implanted Commercially Available Monofocal IOLEXPERIMENTAL -
Bimatoprost-Drug Ring System Low Dose with SpyGlass IOL (IOL with silicone pads (no drug))EXPERIMENTAL -
Bimatoprost-Drug Ring System High Dose with SpyGlass IOL (IOL with silicone pads (no drug))EXPERIMENTAL -

Interventions

NameTypeDescription
BIM-DRS Low DoseDRUGBimatoprost-Drug Ring System Low Dose
BIM-DRS High DoseDRUGBimatoprost-Drug Ring System High Dose
SpyGlass IOL with silicone pads (no drug)DEVICESpyGlass Intraocular Lens with silicone pads (no drug)
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Eligibility Criteria

Age Range22 Years to N/A
SexALL
Healthy VolunteersNo

Inclusion Criteria: * Diagnosis of mild to moderate open-angle glaucoma or ocular hypertension * Pseudophakic or planned removal of cataract * Female participants of childbearing potential must have a negative urine pregnancy test at the baseline visit and agree to the use of contraception Exclusi...

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Frequently asked questions about BIM-DRS

What is BIM-DRS Low Dose used for?

BIM-DRS Low Dose is an investigational small molecule being developed for glaucoma. It is designed for pseudophakic patients diagnosed with open angle glaucoma or ocular hypertension. The drug is delivered through a drug ring system and is currently in Phase 1 clinical development.

What does BIM-DRS Low Dose target?

BIM-DRS Low Dose targets the PTGER2 receptor. This target is relevant to the treatment of glaucoma and ocular hypertension. The drug is being studied for its safety, efficacy, and dose response in patients with these conditions.

Who makes BIM-DRS Low Dose?

BIM-DRS Low Dose is being developed by SpyGlass Pharma, Inc., a company traded under the ticker SGP. The developer is conducting clinical research to evaluate the drug's potential in treating glaucoma and ocular hypertension.

What phase is BIM-DRS Low Dose in?

BIM-DRS Low Dose is in Phase 1 clinical development. It is an investigational drug and has not yet been approved by regulatory authorities. The ongoing Phase 1 trial is designed to assess safety, efficacy, and dose response in patients with open angle glaucoma or ocular hypertension.

What clinical trials is BIM-DRS Low Dose in?

BIM-DRS Low Dose is being evaluated in one active Phase 1 clinical trial with the identifier NCT07641296. The trial is titled 'Evaluation of the Safety, Efficacy, Dose Response of the Bimatoprost Drug Ring System (BIM-DRS) in Pseudophakic Patients Diagnosed With Open Angle Glaucoma or Ocular Hypertension' and has an enrollment target of 24 participants.