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United Medical Research Institute | Inglewood, CA

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AGN-193408 SR in the Treatment of Open-angle Glaucoma or Ocular Hypertension

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Status and phase

Enrolling
Phase 2
Phase 1

Conditions

Open-angle Glaucoma
Ocular Hypertension

Treatments

Other: Lumigan Vehicle
Other: Lumigan
Drug: AGN-193408 SR
Other: Sham Administration

Study type

Interventional

Funder types

Industry

Identifiers

NCT04499248
1833-201-407

Details and patient eligibility

About

This is a multicenter, open-label, dose escalation (Cohort 1) to masked, randomized, parallel-groups (Cohort 2) and (Cohort 3) study to evaluate the safety and efficacy of AGN-193408 SR in participants with open-angle glaucoma or ocular hypertension

Enrollment

96 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participant is willing to withhold his/her IOP (Intraocular Pressure) treatments according to the study requirements, and in the opinion of the investigator, can do so without significant risk.
  • Diagnosis of either OAG [open-angle glaucoma] (ie, [POAG], pseudoexfoliation glaucoma,pigmentary glaucoma) or OHT (ocular hypertension) in both eyes.
  • Must be pseudophakic (at least 4 months postcataract surgery prior to treatment administration [Cycle 1 Day 1 Administration visit]) in the study eye (Cohort 3 only).

Exclusion criteria

  • Known allergy or sensitivity to any study medication or its components, any component of the delivery vehicle, procedure-related materials, or diagnostic agents used during the study (eg, topical anesthetic, dilating drops, fluorescein, povidone-iodine).

  • Concurrent or anticipated enrollment in an investigational drug or device study or participation in such a study within 2 months prior to the Baseline visit through the final study visit.

  • History of intracameral implant in the study eye (eg, Bimatoprost SR, OTX-TIC, ENV515 Travoprost XR).

  • History of laser trabeculoplasty within 6 months prior to screening in the study eye.

  • History or evidence of clinically relevant, substantial ocular trauma (eg, a traumatic cataract, traumatic angle recession, etc.) in the study eye.

  • History or evidence of complicated cataract/lens surgery, as stated in the protocol.

  • Intraocular surgery (including cataract surgery) in the study eye within the 4 months prior to treatment administration.

  • Any history of corneal graft, including partial grafts (eg, Descemet's Stripping Endothelial Keratoplasty [DSEK], Descemet's Membrane Endothelial Keratoplasty [DMEK]); or incisional refractive surgery (eg, radial keratotomy), other than astigmatic keratotomy or limbal relaxing incisions in the study eye.

  • History of herpetic ocular diseases in either eye (including herpes simplex virus and varicella zoster virus).

  • Anticipated need for any incisional or laser ocular surgery in either eye during the study.

  • History of anatomically narrow angle resulting in evidence of angle changes or any history or closed angle glaucoma in the study eye.

  • History or evidence of a peripheral iridotomy/iridectomy in the inferior iris in the study eye.

  • Any history of trabeculectomy or other types of incisional glaucoma surgery, including a glaucoma seton or aqueous bypass stents in either eye, or minimally invasive glaucoma surgery (MIGS) type trabecular meshwork surgeries in the study eye.

  • Anticipated use of corticosteroids in either eye except for permitted interventions or systemically during the study, or historical use prior to Baseline within:

    • 3 years: intraocular fluocinolone acetonide
    • 6 months: intraocular corticosteroid(s) other than fluocinolone; any injectable periocular or sub-Tenon's/subconjunctival corticosteroid
    • 2 months: systemic (eg, oral, intramuscular, intravenous) or topical ocular corticosteroids
    • 2 weeks: dermal corticosteroids applied to skin of the eyelid(s), around the eye, or adnexa.
  • Anticipated use of other topical ocular medications in either eye except for permitted interventions.

  • The anticipated wearing of contact lenses in the study eye (Cohort 1) and both eyes (Cohorts 2 and 3) during the study that deviates from the following (contact lens wear is allowed during the study, but is to be temporarily discontinued before study visits, and before and after an Administration Day according to the following):

    • Use of soft lenses should be discontinued at least 3 days prior to Baseline, and use of rigid gas permeable or hard contact lenses should be discontinued at least 1 week prior to Baseline
    • Use of soft lenses should be discontinued at least 3 days and use of rigid gas permeable or hard contact lenses should be discontinued at least 1 week prior to a scheduled study visit or Administration Day visit
    • Use of contact lenses of any kind should be discontinued for 1 week following any AGN-193408 SR administration
  • Central corneal thickness of < 480 or > 620 micrometers in both eyes.

  • Visual field loss in the study eye that, in the opinion of the investigator, is functionally significant (eg, split fixation, field defect within the central 10 degrees that is visually significant or likely to cause central visual impairment upon progression) or shows evidence of progressive visual field loss within the year prior to Baseline.

  • Evidence of macular edema in either eye during screening or in participant's medical history.

  • At Screening, evidence of posterior synechia behind the iris inferiorly in the study eye that in the investigator's opinion may inhibit the ability to safely receive at least 1 AGN-193408 SR implant (Cohort 3 only).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

96 participants in 6 patient groups

Cohort 1 -Dose A
Experimental group
Description:
Single dose of AGN-193408 SR Dose A administered in the study eye on Day 1. One drop of Lumigan 0.01% administered in the non-study eye once daily every evening starting on Day 1.
Treatment:
Drug: AGN-193408 SR
Other: Lumigan
Cohort 1 - Dose B
Experimental group
Description:
Single dose of AGN-193408 SR Dose B administered in the study eye on Day 1. One drop of Lumigan 0.01% administered in the non-study eye once daily every evening starting on Day 1.
Treatment:
Drug: AGN-193408 SR
Other: Lumigan
Cohort 2 - Dose A
Experimental group
Description:
AGN-193408 SR Dose A (single dose on Day 1) + vehicle eye drops (once daily in the evening starting on Day 1) administered in the study eye. Lumigan (once daily in the evening starting on Day 1) + Sham AGN-193408 SR (single administration on Day 1) administered in the non-study eye.
Treatment:
Other: Sham Administration
Drug: AGN-193408 SR
Other: Lumigan Vehicle
Other: Lumigan
Cohort 2 -Dose B
Experimental group
Description:
AGN-193408 SR Dose B (single dose on Day 1) + vehicle eye drops (once daily in the evening starting on Day 1) administered in the study eye. Lumigan (once daily in the evening starting on Day 1) + Sham AGN-193408 SR (single administration on Day 1) administered in the non-study eye.
Treatment:
Other: Sham Administration
Drug: AGN-193408 SR
Other: Lumigan Vehicle
Other: Lumigan
Cohort 3 - Dose A
Experimental group
Description:
AGN-193408 SR Dose A (single dose on Day 1) + vehicle eye drops (once daily in the evening starting on Day 1) administered behind the study eye. Lumigan (once daily in the evening starting on Day 1) + Sham AGN-193408 SR (single administration on Day 1) administered in the non-study eye.
Treatment:
Other: Sham Administration
Drug: AGN-193408 SR
Other: Lumigan Vehicle
Other: Lumigan
Cohort 3 -Dose B
Experimental group
Description:
AGN-193408 SR Dose B (single dose on Day 1) + vehicle eye drops (once daily in the evening starting on Day 1) administered behind the study eye. Lumigan (once daily in the evening starting on Day 1) + Sham AGN-193408 SR (single administration on Day 1) administered in the non-study eye.
Treatment:
Other: Sham Administration
Drug: AGN-193408 SR
Other: Lumigan Vehicle
Other: Lumigan

Trial contacts and locations

33

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Central trial contact

ABBVIE CALL CENTER

Data sourced from clinicaltrials.gov

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