Travoprost
FDA-approved product (solution/drops, ophthalmic), marketed as Idose Tr, Izba, Travatan and 2 more.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Glaucoma
- Ocular hypertension
- Open-angle glaucoma
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Prostaglandin analogues
- FDA pharmacologic class
- Prostaglandin Analog FDA label ↗
- Anti-infective classification
- Not classified as an anti-infective.
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against MRSA, E. coli and M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA47.7% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli40.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae25.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis59.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.
Evidence
Clinical and experimental
Documented evidenceClinical
50+registered studies name this medicine, for any condition. The registry search keeps the first 50, so there may be more. See them below.
Experimental
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
Docking
Computational · nothing measuredDihydrofolate reductase ↗ (E. coli)
Not yet docked: queued in the docking rundetails
KPC-2 carbapenemase ↗ (K. pneumoniae)
Not yet docked: queued in the docking rundetails
Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)
Not yet docked: queued in the docking rundetails
Dihydrofolate reductase ↗ (MRSA)
Not yet docked: queued in the docking rundetails
AutoDock Vina, one experimentally solved protein per pathogen. This project’s screening target is -7.0 kcal/mol, its own mark rather than a universal cutoff. A docking score is a structural hypothesis, not proof of binding, and requires experimental validation.
Other medicines to investigate
AI prediction · nothing measuredOther repurposing candidates: approved medicines besides Travoprost with AI-predicted activity ≥40% against the chosen pathogen, leaving out existing antimicrobials. They are computational candidates for further investigation, not alternatives and not recommendations.
Sorted by AI-predicted activity, high to low. The order is not a ranking of which medicine is better.
- Etrasimod ArginineExisting use: Ulcerative colitis64.1% AI-predicted activityagainst MRSANo documented evidence found
- MethotrexateExisting use: Acute lymphoblastic leukemia, Adenoma, Arthritis and 21 more64.1% AI-predicted activityagainst MRSA50+ registered studies
- KetoconazoleExisting use: Adrenal gland disease, Blastomycosis, Cushing syndrome and 3 more63.6% AI-predicted activityagainst MRSA50+ registered studies
- LevoketoconazoleExisting use: Adrenal gland disease, Adrenal gland hyperfunction, Cushing syndrome63.6% AI-predicted activityagainst MRSA6 registered studies
- Nafarelin AcetateExisting use: Endometriosis63.6% AI-predicted activityagainst MRSA12 registered studies
- Pafolacianine SodiumExisting use: Other diagnostic agents63.6% AI-predicted activityagainst MRSA1 registered study
- Vinorelbine TartrateExisting use: Cancer, Neoplasm63.6% AI-predicted activityagainst MRSA50+ registered studies
- Ibrexafungerp CitrateExisting use: Vulvovaginal candidiasis63.5% AI-predicted activityagainst MRSANo documented evidence found
- Gonadorelin AcetateExisting use: Gonadotropin-releasing hormones, Tests for fertility disturbances63.4% AI-predicted activityagainst MRSA50+ registered studies
- Icatibant AcetateExisting use: Angioedema, Hereditary angioedema63.4% AI-predicted activityagainst MRSA33 registered studies
- LonafarnibExisting use: Hutchinson-Gilford progeria syndrome, Laminopathies, Progeria63.3% AI-predicted activityagainst MRSA39 registered studies
- LypressinExisting use: Vasopressin and analogues63.2% AI-predicted activityagainst MRSA50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Trial to Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant
NCT07495852 · start 2026-02-17
Registered record
- Registry ID
- NCT07495852
- Conditions
- Glaucoma
- Interventions
- Gen 2 Travoprost Intracameral Implant; Timolol eye drops 0.5%; Sham Procedure; placebo eye drops
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2026-02-17
- Completion
- 2032-03
- Enrolment
- 510
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGlaucomaInterventionGen 2 Travoprost Intracameral Implant; Timolol eye drops 0.5%; Sham Procedure; placebo eye dropsPhasePhase 3Registry statusRecruitingObservational Trial of the Updated Inserter for the Travoprost Intracameral Implant 75mcg
NCT07400926 · start 2025-12-17
Registered record
- Registry ID
- NCT07400926
- Conditions
- Open Angle Glaucoma (OAG); Ocular Hypertension (OH)
- Interventions
- Travoprost
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2025-12-17
- Completion
- 2026-07
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOpen Angle Glaucoma (OAG); Ocular Hypertension (OH)InterventionTravoprostPhaseNot recordedRegistry statusRecruitingPhase 2 Trial to Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant
NCT07075718 · start 2025-06-12
Registered record
- Registry ID
- NCT07075718
- Conditions
- Glaucoma
- Interventions
- Gen 2 Travoprost Intracameral Implant; Timolol eye drops 0.5%; Sham Procedure; Placebo eye drops
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2025-06-12
- Completion
- 2032-03
- Enrolment
- 110
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGlaucomaInterventionGen 2 Travoprost Intracameral Implant; Timolol eye drops 0.5%; Sham Procedure; Placebo eye dropsPhasePhase 2Registry statusRecruitingSafety and Efficacy of iDose® TR With Cataract Surgery vs. Cataract Surgery Alone
NCT06848946 · start 2025-01-13
Registered record
- Registry ID
- NCT06848946
- Conditions
- Glaucoma, Open-angle; Ocular Hypertension (OHT); Phacoemulsification Cataract Surgery
- Interventions
- iDose TR (travoprost intracameral implant) 75 µg in conjunction with cataract surgery; Sham procedure in conjunction with cataract surgery
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2025-01-13
- Completion
- 2027-06
- Enrolment
- 132
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGlaucoma, Open-angle; Ocular Hypertension (OHT); Phacoemulsification Cataract SurgeryInterventioniDose TR (travoprost intracameral implant) 75 µg in conjunction with cataract surgery; Sham procedure in conjunction with cataract surgeryPhasePhase 4Registry statusRecruitingPSLT Compared to Prostaglandin Analogue Eye Drops
NCT05241938 · start 2021-09-01
Registered record
- Registry ID
- NCT05241938
- Conditions
- Open Angle Glaucoma; Ocular Hypertension
- Interventions
- PSLT; Prostaglandin analogue eye drops
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2021-09-01
- Completion
- 2022-12-20
- Enrolment
- 75
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOpen Angle Glaucoma; Ocular HypertensionInterventionPSLT; Prostaglandin analogue eye dropsPhaseNot applicableRegistry statusUnknownPerformance of the Travoprost Intraocular Implant
NCT06582732 · start 2021-03-10
Registered record
- Registry ID
- NCT06582732
- Conditions
- Glaucoma, Open-Angle; Ocular Hypertension
- Interventions
- Travoprost Intracameral Implant exchanged at Month 12; Travoprost Intracameral Implant exchanged at Month 3; Travoprost Intracameral Implant exchanged at Month 6; Travoprost Intracameral Implant exchanged at Month 24; Travoprost intracameral implant exchanged at Month 21; Travoprost intracameral implant exchanged at Month 18; Travoprost intracameral implant exchanged at Month 15
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2021-03-10
- Completion
- 2023-11-02
- Enrolment
- 210
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGlaucoma, Open-Angle; Ocular HypertensionInterventionTravoprost Intracameral Implant exchanged at Month 12; Travoprost Intracameral Implant exchanged at Month 3; Travoprost Intracameral Implant exchanged at Month 6; Travoprost Intracameral Implant exchanged at Month 24 +3 morePhasePhase 2Registry statusCompletedInterval Intraocular Pressure in Intravitreal Injection Study
NCT04868175 · start 2019-10-01
Registered record
- Registry ID
- NCT04868175
- Conditions
- Glaucoma; Intraocular Pressure
- Interventions
- Timolol; Travatan; Hypromellose
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2019-10-01
- Completion
- 2021-04-01
- Enrolment
- 64
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGlaucoma; Intraocular PressureInterventionTimolol; Travatan; HypromellosePhaseNot applicableRegistry statusCompletedComparison Between Latanoprost , Travoprost and Tafluprost in Reducing IOP Fluctuation in POAG Patients
NCT04461249 · start 2019-06-01
Registered record
- Registry ID
- NCT04461249
- Conditions
- Primary Open Angle Glaucoma
- Interventions
- Latanoprost 0.005% Ophthalmic Solution; Travoprost 0.004% ophthalmic solution; Tafluprost Ophthalmic 0.0015% Ophthalmic Solution
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2019-06-01
- Completion
- 2020-04-01
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPrimary Open Angle GlaucomaInterventionLatanoprost 0.005% Ophthalmic Solution; Travoprost 0.004% ophthalmic solution; Tafluprost Ophthalmic 0.0015% Ophthalmic SolutionPhaseNot recordedRegistry statusCompletedA Study to Evaluate the Long Term Safety of OTX-TP (Sustained Release Travoprost) Intracanalicular Insert
NCT04061044 · start 2018-07-10
Registered record
- Registry ID
- NCT04061044
- Conditions
- Open Angle Glaucoma and Ocular Hypertension
- Interventions
- Ophthalmic Insert
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2018-07-10
- Completion
- 2020-09-22
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOpen Angle Glaucoma and Ocular HypertensionInterventionOphthalmic InsertPhasePhase 3Registry statusCompletedPhase 3 Study Evaluating Safety and Efficacy of OTX-TP in Subjects With OAG or OHT
NCT02914509 · start 2016-11-07
Registered record
- Registry ID
- NCT02914509
- Conditions
- Open Angle Glaucoma; Ocular Hypertension
- Interventions
- Travoprost; Placebo Vehicle
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2016-11-07
- Completion
- 2019-03-30
- Enrolment
- 565
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOpen Angle Glaucoma; Ocular HypertensionInterventionTravoprost; Placebo VehiclePhasePhase 3Registry statusCompletedGeneric Travoprost Versus Brand Name Travoprost in Patients With Primary Open Angle Glaucoma or Ocular Hypertension
NCT02796560 · start 2016-07-01
Registered record
- Registry ID
- NCT02796560
- Conditions
- Glaucoma, Primary Open Angle; Ocular Hypertension
- Interventions
- Brand name travoprost; Generic travoprost
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2016-07-01
- Completion
- 2017-09-12
- Enrolment
- 76
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGlaucoma, Primary Open Angle; Ocular HypertensionInterventionBrand name travoprost; Generic travoprostPhasePhase 4Registry statusCompletedEfficacy of Travoprost/Timolol for Uncontrolled Intraocular Pressure
NCT02003391 · start 2013-12
Registered record
- Registry ID
- NCT02003391
- Conditions
- Open Angle Glaucoma; Ocular Hypertension
- Interventions
- Beta-blocker monotherapy; Travoprost 0.004% / timolol 0.5% fixed combination ophthalmic solution
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2013-12
- Completion
- 2015-05
- Enrolment
- 157
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOpen Angle Glaucoma; Ocular HypertensionInterventionBeta-blocker monotherapy; Travoprost 0.004% / timolol 0.5% fixed combination ophthalmic solutionPhasePhase 4Registry statusCompletedMulti-Arm Feasibility Study Evaluating OTX-TP Compared to Timolol in Treatment of Subjects With Open Angle Glaucoma
NCT01845038 · start 2013-04
Registered record
- Registry ID
- NCT01845038
- Conditions
- Glaucoma
- Interventions
- OTX-TPa ~4µg/day over 2 mos. with natural tears drops; OTX-TPb ~3µg/day over 3 months with natural tears drops; Timolol Maleate (0.5%) dosed twice daily with punctum plug without drug
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2013-04
- Completion
- 2014-05
- Enrolment
- 41
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGlaucomaInterventionOTX-TPa ~4µg/day over 2 mos. with natural tears drops; OTX-TPb ~3µg/day over 3 months with natural tears drops; Timolol Maleate (0.5%) dosed twice daily with punctum plug without drugPhasePhase 1Registry statusCompletedTwo Trabecular Micro-bypass Stents & Postoperative Travoprost to Treat Glaucoma Subjects on Two Hypotensive Agents
NCT02873806 · start 2013-03
Registered record
- Registry ID
- NCT02873806
- Conditions
- Open-angle Glaucoma
- Interventions
- Implantation of two iStent inject micro-bypass stents; Topical travoprost; Two iStent inject micro-bypass stents; Tobramycin; Dexamethasone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2013-03
- Completion
- 2019-11-08
- Enrolment
- 53
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOpen-angle GlaucomaInterventionImplantation of two iStent inject micro-bypass stents; Topical travoprost; Two iStent inject micro-bypass stents; Tobramycin +1 morePhasePhase 4Registry statusCompletedAn Efficacy and Tolerability Study of TRAVATAN® Versus LUMIGAN®
NCT01664039 · start 2012-09
Registered record
- Registry ID
- NCT01664039
- Conditions
- Glaucoma; Ocular Hypertension
- Interventions
- Travoprost 0.004% ophthalmic solution; Bimatoprost 0.01% ophthalmic solution
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2012-09
- Completion
- 2014-06
- Enrolment
- 104
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGlaucoma; Ocular HypertensionInterventionTravoprost 0.004% ophthalmic solution; Bimatoprost 0.01% ophthalmic solutionPhasePhase 4Registry statusCompleted