PARKHURST NUVISION

iDose TR

Travoprost intracameral implant
Gurpal Virdi, MD
Glaukos · FDA-approved Dec 2023 · U.S. launch 2024

The problem drops don't solve

iDose TR is a pillar of "interventional glaucoma" — moving from drops to procedures earlier

  • Adherence. Roughly half of glaucoma patients aren't taking drops as prescribed within a year.
  • Preservative toxicity & ocular surface disease. Chronic BAK exposure drives redness, burning, and unstable tear film.
  • Prostaglandin-associated periorbitopathy (PAP). Orbital fat atrophy, deepened sulcus, lash changes.
  • The pitch: a one-time, in-office implant that removes the daily-drop burden while it works.

What it is

  • Titanium implant, 1.8 × 0.5 mm — smaller than a grain of rice.
  • 75 mcg of preservative-free travoprost held in a reservoir.
  • Elutes continuously into the anterior chamber by membrane-controlled diffusion — steady drug level, no daily dosing.
  • Implanted through the trabecular meshwork and back wall of Schlemm's canal, anchored in scleral tissue.
1.8 × 0.5 mm
Titanium reservoir implant
75 mcg
Preservative-free travoprost
Continuous
Membrane-controlled elution
Glaukos · FDA-approved December 2023, U.S. launch 2024.

Travoprost & the prostaglandin analogs

  • Travoprost is a prostaglandin F2α analog — same class as latanoprost, bimatoprost, tafluprost, and the most potent topical IOP-lowering class (~25–33%).
  • Prodrug → FP-receptor agonist. Corneal esterases convert it to travoprost free acid, which lowers IOP mainly by increasing uveoscleral outflow.
  • Delivery is the differentiator, not the molecule — efficacy across PGAs is broadly similar; iDose changes how the drug is delivered.
  • Preservative-free, intracameral, negligible systemic exposure — plasma travoprost stays below the assay limit (<10 pg/mL); it bypasses the ocular surface.
Fewer surface & cosmetic effects than drops: much less hyperemia, and trials saw none of the iris / periorbital pigmentation typical of topical PGAs — though the label still lists possible, likely-permanent iris pigmentation.
Source: iDose TR prescribing information (Glaukos), 1/2026.

How it goes in

  • Clear corneal incision, aseptic conditions — in-office or OR.
  • Delivered across the angle and anchored at the iridocorneal angle.
  • Gonioscopy-visible — confirm position at the slit lamp.
  • Standalone or combined with cataract surgery.
iDose implantation — watch on YouTube
Implantation across the angle — watch on YouTube

Who it's for

  • Mild-to-moderate open-angle glaucoma or ocular hypertension needing better IOP control.
  • Patients with poor adherence or intolerance to topical drops.
  • Ocular surface disease, dexterity limits, or cost barriers to daily drops.
  • Can be performed with or without cataract surgery.

Contraindications & cautions

Contraindicated

  • Active or suspected ocular / periocular infection
  • Corneal endothelial dystrophy — Fuchs, guttata
  • Prior corneal transplant or DSAEK
  • Hypersensitivity to travoprost

Use caution / counsel

  • Narrow angles or angle abnormalities
  • Monitor routinely to confirm implant position
  • Iris pigmentation can occur — likely permanent
  • MRI conditional — a handy practical pearl
Why the corneal ones: the implant sits by the corneal endothelium — Fuchs/guttata and prior grafts have too little endothelial reserve to absorb further cell loss.
Sources: iDose TR HCP prescribing information; Glaukos.
Just changed — Jan 28, 2026

Re-administration is now approved

  • FDA approved a labeling supplement allowing re-administration in the same eye — the old label said don't re-dose.
  • Requires specular microscopy: the eye must meet an age-based minimum endothelial cell density; re-dosing is withheld if there's ≥10% ECD loss or prior device dislocation.
  • No more than once per year.
  • Backed by no clinically significant endothelial cell loss through 3 years across the phase 3 / 2b studies.
  • Exchange study: place the new implant first, then remove the old one — safe and tolerated over 12 months.
Sources: Glaukos; PentaVision. FDA approval Jan 28, 2026.

Where iDose sits in sustained-release glaucoma

SystemDrug & formatDurationStatus
iDose TR Travoprost — titanium, non-biodegradable, re-dosable Label ~3 yr FDA approved 2023
Durysta Bimatoprost — biodegradable intracameral ~3–4 mo FDA approved 2020
OTX-TIC Travoprost — biodegradable hydrogel 4–6 mo Phase 3 (missed endpoint)
ENV515 Travoprost XR — biodegradable ~6 mo Phase 2a
SpyGlass Bimatoprost — drug-eluting IOL pads (at cataract) Up to 3 yr Phase 1/2
Takeaway: iDose & Durysta are the only FDA-approved intracameral implants — iDose is the only non-biodegradable, re-administrable one, giving it by far the longest duration.
Investigational agents shown for context; landscape per published reviews.
Our clinic's perspective — not Glaukos data

How iDose fits our MIGS toolkit

OptionIndicationOn a med?IOP dropNotes
iDose TR Mild–moderate OAG + ocular HTN Not required ~20–25% Continuous travoprost; can get OHT / one-med patients off drops
iStent Infinite
(3 stents)
Mild–moderate OAG Required — must be on a med ~15–20% (if lucky) Not for ocular HTN; best when noncompliant or poor ocular surface
OMNI Ocular HTN + mild–moderate Not required Largest drop Usually 2+ meds / more moderate disease; ↑ hyphema & cyclodialysis-cleft risk → historically after iStent
ECP Closed-angle cases For closed angles; also driven by insurance coverage
Our clinic's perspective — not Glaukos data

What we see in clinic

  • iDose — for ocular hypertension or a one-med patient, we can often get them off drops entirely. Labeling supports ~3 years; in our hands we typically see ~2 years of effect.
  • iStent — anecdotally a temporary drop holiday, but many are back on a drop within 1–2 years.
  • OMNI gives the biggest IOP reduction — we reserve it for 2+ meds / more moderate disease, and historically place it after iStent given higher hyphema and cyclodialysis-cleft risk.
  • ECP — we use in closed-angle eyes, and where insurance coverage favors it.
Enrolling now · Parkhurst NuVision

Our iDose + iStent study

The study

  • All qualifying patients receive iDose TR; 20% randomized to also get 3 iStent infinite stents
  • One eye · 12-month follow-up
  • Goal: safety & IOP-lowering efficacy of iDose TR + iStent infinite
  • Patients reimbursed $1,050

Who qualifies — refer if…

  • Age 18+, any sex
  • Glaucoma or ocular hypertension
  • On 0–2 IOP-lowering medications
  • No prior incisional glaucoma surgery
Have a patient who fits? Send them to Parkhurst NuVision for screening.
Study sponsored by Glaukos; conducted at Parkhurst NuVision.

Managing the postop patient

  • Postop course resembles other trabecular MIGS — minimal inflammation, quick recovery.
  • Expect gradual IOP lowering as travoprost releases; effect may not be immediate.
  • Continue preop drops initially, then taper based on IOP response and your discretion.
  • Monitor IOP, inflammation, corneal status at routine intervals (POD1 if combined, then 1–4 wks).
  • Gonioscopy confirms implant position if IOP response is suboptimal.
  • Reinforce this is not a cure — ongoing glaucoma monitoring is still required.

Coverage & coding

  • Medicare + true supplemental insurance cover iDose — minimal out-of-pocket for most patients.
  • Available buy-and-bill or via specialty pharmacy (physician isn't paid for the drug if via specialty pharmacy).
Sources: Eyes On Eyecare; American Academy of Ophthalmology; our clinic's billing experience.

Who to send us

Great candidates

  • Mild-to-moderate OAG / ocular hypertension
  • Poor compliance / drop-intolerant
  • Uncomfortable eyes — poor or damaged ocular surface
  • Dexterity or cost barriers
  • Anyone heading to cataract surgery — combine it

Not for

  • Fuchs / guttata
  • Prior corneal graft
  • Narrow angles
  • Advanced disease needing a low target
Refer for an iDose TR consultation

Thank you

Let's connect — Gurpal Virdi, MD · scan to follow or reach out

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