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Travoprost

Phase 3

Glaucoma, Angle-Closure | Small molecule | Ophthalmology |Alcon Inc.|Last Updated: Jul 10, 2014

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindUNCONTROLLED
Total Trials1
Total Enrollment -

FDA Designations

No designations recorded

Clinical trial landscape

Travoprost · 4 trials · 4 indications

Phase 3 3Phase 2 1
NCT00051142A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Open-Angle Glaucoma (OAG) or Ocular Hypertension (OHT)Glaucoma, Open-Angle
COMPLETED- Analytics
NCT00051155A 6-Week Safety and Efficacy Study of Travatan Compared to Xalcom in Subjects With Open-Angle Glaucoma(OAG) or Ocular Hypertension(OHT)Glaucoma, Open-Angle
COMPLETED- Analytics
NCT00051181A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Chronic Angle-Closure GlaucomaGlaucoma, Angle-Closure
COMPLETED- Analytics
PHASE3COMPLETED
A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Open-Angle Glaucoma (OAG) or Ocular Hypertension (OHT)
Glaucoma, Open-AngleUnlock trial analytics
PHASE3COMPLETED
A 6-Week Safety and Efficacy Study of Travatan Compared to Xalcom in Subjects With Open-Angle Glaucoma(OAG) or Ocular Hypertension(OHT)
Glaucoma, Open-AngleUnlock trial analytics
PHASE3COMPLETED
A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Chronic Angle-Closure Glaucoma
Glaucoma, Angle-ClosureUnlock trial analytics

Study Endpoints

Primary Endpoints

Mean change from baseline in intraocular pressure (IOP)
Baseline, Up to Week 4

IOP (fluid pressure inside the eye) was measured by Goldmann applanation tonometry. A higher IOP can be a greater risk for developing glaucoma or glaucoma progression (leading to optic nerve damage). A more negative change indicates a greater amount of improvement.

Secondary Endpoints

Mean intraocular pressure
Baseline, Up to Week 4
Mean percent change from baseline in IOP
Baseline, Up to Week 4
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Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Travoprost new formulationEXPERIMENTALTravoprost ophthalmic solution (new formulation), 1 of 3 dose levels, 1 drop in the study eye(s) once daily, at 8 PM, for 4 weeks
TRAVATANACTIVE_COMPARATORTravoprost ophthalmic solution 0.004%, 1 drop in the study eye(s) once daily, at 8 PM, for 4 weeks
VehiclePLACEBO_COMPARATORInactive ingredients, 1 drop in the study eye(s) once daily, at 8 PM, for 4 weeks

Interventions

NameTypeDescription
TravoprostDRUG -
LatanoprostDRUG -
Travoprost (0.004%)DRUG -
Latanoprost (0.005%)/Timolol (0.5%)DRUG -
Latanoprost (0.005%)DRUG -
Travoprost ophthalmic solution (new formulation)DRUG -
Travoprost ophthalmic solution, 0.004%DRUG -
VehicleDRUGInactive ingredients used as a placebo
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites1

Adult patients of any race and either sex with open-angle glaucoma (with or without pigment dispersion or pseudoexfoliation component) or ocular hypertension.

Countries:United StatesAustralia
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Frequently asked questions about Travoprost

What is Travoprost used for?

Travoprost is used for lowering intraocular pressure in patients with ocular hypertension and glaucoma, including open-angle glaucoma and angle-closure glaucoma. It is a small molecule developed by Alcon Inc. for the ophthalmology therapeutic area and is currently in Phase 3 clinical development.

What does Travoprost target?

Travoprost is a prostaglandin analog that works by increasing the outflow of aqueous humor from the eye, thereby reducing intraocular pressure. It is being studied for its efficacy in treating open-angle glaucoma and ocular hypertension, with clinical trials comparing it to other prostaglandin analogs.

Who makes Travoprost?

Travoprost is developed by Alcon Inc., a company traded under the ticker symbol ALC. Alcon is conducting clinical trials to evaluate the safety and efficacy of Travoprost in patients with glaucoma and ocular hypertension.

What phase is Travoprost in?

Travoprost is in Phase 3 clinical development. It has completed five clinical trials, including Phase 3 studies, with a total enrollment of 1,549 participants. The drug is investigational and not yet approved by regulatory authorities.

What clinical trials is Travoprost in?

Travoprost has been studied in several clinical trials, including NCT00051142 and NCT00051155, which are Phase 3 trials comparing Travoprost to other glaucoma medications. Additional Phase 2 trials, such as NCT00637130 and NCT01298687, have also been completed to evaluate its safety and efficacy.

Is Travoprost the same as Travatan?

Travoprost is also known by the brand name Travatan. Clinical trials, such as NCT01298687, refer to the drug as TRAVATAN, confirming that Travoprost and Travatan are the same medication.