NDAINTRACAMERALIMPLANT
Approved
Dec 2023
Lifecycle
Growth
Competitive Pressure
8/100
Clinical Trials
4
Data completeness
4/8 — Partial
IDOSE TR (travoprost intracameral) by Glaukos. Approved for prostaglandin analog [epc]. First approved in 2023.
Drug data last refreshed 15h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
IDOSE TR is an intracameral implant containing travoprost, a prostaglandin analog approved in December 2023 for reducing intraocular pressure in glaucoma patients. The implant delivers travoprost directly into the anterior chamber of the eye, providing sustained drug release over an extended period. This novel formulation represents a shift from topical prostaglandin therapy toward depot-based intraocular delivery.
Growth4.6 years to LOE
Early-stage growth product with significant competitive pressure (score 8/10) offering opportunities for teams building market presence in a novel delivery modality.
Mechanism of Action
Pharmacologic Class:
Prostaglandin Analog
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (4)
Trial to Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant
Started Feb 2026
510 enrolled
Glaucoma
Standalone iStent Infinite and iDose TR for Management of Moderate to Severe Open Angle Glaucoma
Started Jan 2026
20 enrolled
Open Angle GlaucomaPigmentary GlaucomaPseudoexfoliation Glaucoma
Observational Trial of the Updated Inserter for the Travoprost Intracameral Implant 75mcg
Started Dec 2025
30 enrolled
Open Angle Glaucoma (OAG)Ocular Hypertension (OH)
Phase 2/Phase 3 Trial to Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant
Started Jun 2025
610 enrolled
Glaucoma
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.