Travosant Forte™

 The Next Generation of Canine Glaucoma.                                               Triple Therapy in One Step. 

Upcoming Free Webinar

Next-Generation Medical Therapy & Ocular Surface Restoration in Canine Glaucoma and Dry Eye Disease

Wednesday, May 20th | 8 p.m. ET

This medical CE program provides veterinarians and veterinary technicians with advanced clinical training in emerging medical therapy for canine glaucoma and dry eye disease (DED/KCS). The course explores the interaction between intraocular pressure dynamics, ocular surface inflammation, and tear film integrity, with specific emphasis on the role of novel lipid-base ocular surface formulations used in conjunction with advanced tear replacers to promote long-term corneal health and visual function.

Glaucoma: An Insidious Disease

Glaucoma is a group of ocular disorders characterized by elevated intraocular pressure (IOP) that can progressively impair vision if unmanaged. Medical therapy to reduce IOP is recommended to delay onset and slow disease progression. However, many canine patients require multiple ocular hypotensive medications to achieve and maintain physiological IOP levels.

Our Partnership with Santgar™

Stokes Healthcare is proud to partner with Santgar, a leading veterinary pharmaceutical innovator in Mexico known for its research-driven, high-quality animal health solutions. Santgar sought us out for this collaboration, recognizing our product quality, rigorous processes, and shared commitment to the same standards and values. Together, we are introducing new ophthalmic formulations to the U.S. market, expanding access to advanced veterinary therapies and improving patient outcomes.

Santgar Logo (with TM)

Travosant Forte™: Triple Fixed Combination for IOP Control

Clinical evidence in glaucoma patients consistently demonstrates that combination pressure-lowering therapies reduce IOP more than monotherapy, with comparable or improved tolerability profiles (Boyle et al., 1998; Fechtner & Realini, 2004).

Travosant Forte® combines three mechanisms of action into a single ophthalmic gel formulation:

  • Dorzolamide 2% – Carbonic anhydrase inhibitor (CAI) that reduces aqueous humor production
  • Betaxolol 0.25% – Selective beta-blocker that inhibits aqueous humor synthesis
  • Travoprost 0.004% – Prostaglandin analogue (PGA) that enhances uveoscleral outflow

This triple-combination therapy delivers robust IOP reduction, achieving 20–30% greater pressure lowering from baseline.

Recommended Dosing:

Instill one drop every 12 hours in affected eye(s) and every 24 hours at night in unaffected eye. (Can adjust dose to every 8 hours in affected eye if needed.)

Important: Treat BOTH eyes even when only one is affected to delay glaucoma onset in the second eye. Travosant Forte works best when administered at consistent times daily. Treatment should be continued on a long term basis in patients in which intraocular pressure tends to remain elevated.

Clinical Advantages

  • Greater IOP reduction compared to monotherapy
  • Improved tolerability profiles
  • Enhanced eye drop adherence
  • Reduced exposure to preservatives
    This triple fixed-combination gel system helps minimize dilution or washout of active ingredients that can occur when multiple medications are administered in close succession.

This triple fixed-combination gel system helps minimize dilution or washout of active ingredients that can occur when multiple medications are administered in close

Practical Benefits for Patients & Pet Owners

  • Fewer bottles
  • Fewer daily applications
  • Improved convenience
  • Better treatment follow-up
  • Increased clinical efficiency

Prescribe for a Patient Today!

Online at iFill.com or call 800-754-5222

Baseline

Eye Before - Copy (2)

Post Treatment

Can Travosant Forte™ be used if I’m not 100% sure it’s glaucoma?

Yes. It is safe in uncertain cases and will not lower pressure in normal eyes.

Yes. Treating both eyes is critical to delaying disease in the second eye.

Travosant Forte™ works through a dual mechanism – it both reduces aqueous humor production and increases fluid drainage from the eye, lowering intraocular pressure (IOP).

What makes it unique is the inclusion of betaxolol, which not only reduces fluid production but also provides a neuroprotective effect. It penetrates to the optic nerve and retina, helping protect nerve cells and optic nerve fibers while pressure is being lowered – something not typically seen in standard glaucoma therapies.

In an acute setting, Travosant Forte™ can be administered every 1–2 hours until intraocular pressure (IOP) decreases to a safer range. Once pressure is controlled, dosing should transition to a maintenance schedule.

Once IOP has stabilized and the patient is clinically improved, dosing can typically be reduced to:

  • Affected eye: 2–3 times daily
  • Unaffected eye: Once daily (at night)

Travosant Forte™ is highly effective at rapidly lowering IOP and may be used as a primary therapy. However, clinical judgment should guide whether additional treatments are needed based on severity and patient response.

In many cases, intraocular pressure begins to decrease within 30 minutes to a few hours.

Yes. Pain relief occurs as pressure decreases – often rapidly.

  • Affected eye: Administer one drop 2–3 times daily
  • Unaffected eye: Administer one drop daily at night

Travosant Forte™ works best when administered at consistent times daily, which helps maintain stable intraocular pressure control.

Eye pressure often increases at night. Evening dosing provides protection during this period.

Yes, but you should wait at least 5 minutes after applying Travosant Forte™ before administering any other ophthalmic medications to ensure proper absorption.

No. Glaucoma requires lifelong management. Stopping treatment will result in pressure rising again.

No withdrawal effects, but untreated periods may allow further optic nerve damage.

Treatment should be continued on a long-term basis in patients where intraocular pressure tends to remain elevated, as glaucoma is a chronic condition requiring ongoing management.

Travosant Forte™ should be used with caution or avoided in certain cases, including:

  • Dogs with significant cardiovascular disease (betaxolol may lower heart rate and blood pressure)
  • Cats with asthma or respiratory disease
  • Patients with known hypersensitivity to any of the components

Use should always be guided by a veterinarian, with monitoring as needed in at-risk patients.

Most patients tolerate Travosant Forte™ well. The gel formulation is designed to be soothing. However, side effects could be burning, stinging or redness of the eye. Long term use of prostaglandins may cause darkening of the iris.

Yes. Travosant Forte™ should be refrigerated to maintain stability and effectiveness.

Travosant Forte™ is compounded in accordance with USP guidelines and is dispensed with the maximum allowable beyond-use date available from a compounding pharmacy. It will have a beyond-use date of approximately 7–30 days from the time of dispensing.

Yes. Travosant Forte™ is used in dogs, cats, and horses. It is most extensively studied in dogs, with additional clinical use showing effectiveness in horses and cats. Because glaucoma differs between species, treatment should always be guided by a veterinarian.

Caution is needed when using prostaglandin analogs in horses with glaucoma associated with uveitis. Uveitis is a leading cause of blindness in adult horses and can contribute to the development of Glaucoma, cataracts, and vascular damage within the eye. If the uveitis is active—indicated by signs such as aqueous flare (inflammation in the anterior chamber)—prostaglandin analogs are generally not recommended, as they may exacerbate inflammation. However, if the uveitis is inactive (no aqueous flare present), the inflammatory process is considered controlled. In these cases, using Travosant Forte™ may be appropriate as part of a glaucoma management plan. Because glaucoma in horses is complex and often multifactorial, treatment decisions should always be based on careful clinical evaluation and ongoing monitoring.

References:
Boyle, J. E., Ghosh, K., Gieser, D. K., & Adamsons, I. A. (1998). A randomized trial comparing the dorzolamide-timolol combination given twice daily to monotherapy with timolol and dorzolamide. Ophthalmology, 105(10), 1945–1951. https://doi.org/10.1016/s0161-6420(98)91046-6
Fechtner, R. D., & Realini, T. (2004). Fixed combinations of topical glaucoma medications. Current Opinion in Ophthalmology, 15(2), 132–135. https://doi.org/10.1097/00055735-200404000-00013