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Visus Therapeutics

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Namestring
Visus Therapeutics
Legal namestring
Visus Therapeutics, Inc.
Websiteurl
visustx.com
Company typeenum
Private
Founded yearint
2017
Descriptiontext

Visus Therapeutics is a clinical-stage ophthalmic pharmaceutical company founded in 2017 and headquartered in Seattle, Washington, that developed Yuvezzi, the first and only FDA-approved fixed-dose combination eye drop for presbyopia. Yuvezzi combines carbachol (a cholinergic agonist) and brimonidine tartrate (an alpha-2 adrenergic agonist) in a single prescription formulation, with Phase 3 trials (536 patients) demonstrating superiority over individual components and a duration of effect of up to 10 hours with no serious adverse effects over 12 months. The company also filed BRIMOCHOL PF (NDA accepted June 2025), a related presbyopia asset within the same chemical family.

In December 2024 Visus merged with Tenpoint Therapeutics Ltd., consolidating pipelines targeting presbyopia, cataracts, and geographic atrophy under a combined entity headquartered at 25 Independence Blvd., Suite 100, Warren, NJ; Visus now operates as an affiliate of Tenpoint. Yuvezzi received FDA approval on January 29, 2026, and is planned for U.S. commercial launch in Q2 2026.

Visus/Tenpoint generates revenue (once launched) through prescription pharmaceutical sales distributed via retail and specialty pharmacies, with prescribing driven through an enterprise field sales motion targeting ophthalmologists and optometrists. The company maintains a dedicated eye care professional portal (yuvezziecp.com) to support prescriber engagement. Pre-launch, the company is pre-revenue; cumulative capital raised totals approximately $235 million, including a $85 million Series B led by Janus Henderson with EQT Nexus, Hillhouse, and the British Business Bank, plus a $150 million debt facility from Hercules Capital. Leadership includes co-founder and CEO Ben Bergo, SVP of Business Development and Marketing Jehan Tamboowalla, and CFO Melissa Epperly.

Short descriptiontext

Visus Therapeutics is a clinical-stage ophthalmic pharmaceutical company that developed Yuvezzi, the first FDA-approved fixed-dose combination eye drop for presbyopia. Now an affiliate of Tenpoint Therapeutics following a December 2024 merger, with U.S. commercial launch planned for Q2 2026.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersSeattle, United States
HQ citystring
Seattle
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
presbyopia eye drops, ophthalmic pharmaceuticals, fixed-dose combination, prescription therapeutics, vision restoration
Industry2 codes
PRIMARYHLAIACAK
Ophthalmology Specialty Pharmaceuticals
SECONDARYHLAHAIAL
Ocular Drug Delivery Devices (Eye Droppers/Inserts)
Healthcare & Life Sciences/Medical Devices & Diagnostics/Drug Delivery Devices (Injectors, Pumps, Inhalers)
NAICS code1 code
  • Ophthalmic Goods Manufacturing339115
SIC code1 code
  • Surgical & Medical Instruments & Apparatus3841
Product category
Ophthalmic Pharmaceuticals
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Prescription Pharmaceutical Sales
TypeOne Time License
Description

Revenue generated from selling prescription eye drop medications (Yuvezzi) through pharmacies and eye care professionals. Launch planned for Q2 2026 following FDA approval.

fiercepharma.com
Marketing channels1 record

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Supply Chain, Marketing or Sales, Operations
GTM typeB2C
B2C
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1Yuvezzi
Description

Presbyopia eye drop treatment combining carbachol and brimonidine tartrate - the first fixed-dose combination therapy for age-related vision condition affecting approximately 2 billion people globally.

fiercepharma.com
Core offering1 text field

Visus Therapeutics develops prescription ophthalmic pharmaceutical products for age-related vision conditions, principally presbyopia. Its lead product, Yuvezzi, is the first FDA-approved fixed-dose combination eye drop combining carbachol and brimonidine tartrate, offering up to 10 hours of functional near vision improvement. The company is also developing BRIMOCHOL PF, a presbyopia candidate in the same therapeutic class.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Phase 3 trials demonstrated superiority over individual components with no serious adverse effects over 12-month safety study
+2 more records
Product overview1 text field

Visus Therapeutics, a Seattle-based company that merged with Tenpoint Therapeutics, developed Yuvezzi as its lead product. Yuvezzi is a dual-agent combination eye drop (carbachol and brimonidine tartrate) designed to treat presbyopia, an age-related vision condition affecting near focus. The company previously filed for NDA for BRIMOCHOL PF, which appears to be related to or part of the same product family. Following the merger, Tenpoint now handles commercialization of Yuvezzi after receiving FDA approval in January 2026.

Product and service1 record
1Yuvezzi
CategoryOphthalmic Pharmaceuticals
Description

Yuvezzi is a prescription dual-agent combination eye drop therapy combining carbachol and brimonidine tartrate, indicated for the treatment of presbyopia (age-related loss of near visual acuity) in adults. It is the first and only fixed-dose combination therapy approved by the FDA for presbyopia, providing up to 10 hours of functional near vision improvement.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierFlagshipTypeStrategic or Co-development Partner
Description

Visus Therapeutics merged with Tenpoint Therapeutics in December 2024 to form a combined company focused on ophthalmic medicines. The merger consolidated pipelines targeting presbyopia, cataracts, and geographic atrophy. Yuvezzi originated from Visus and received FDA approval under the combined entity.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Markets Vuity (pilocarpine 1.25%), the first FDA-approved presbyopia eye drop. Direct therapeutic competitor to Yuvezzi and a broad ophthalmology incumbent with deep commercial reach and prescriber relationships.

TypeDirect peer
Description

Clinical-stage ophthalmic company developing aceclidine-based presbyopia eye drops (LNZ100/LNZ101). Directly competes with Yuvezzi in the prescription presbyopia drop category with a similar regulatory and commercial pathway.

TypeDirect peer
Description

Developed Qlosi (pilocarpine 0.4%), an FDA-approved presbyopia eye drop. Directly competes with Yuvezzi in the same ECP prescribing channel and patient population.

TypeEmerging player
Description

Ophthalmic pharmaceutical company developing microdose array print platform therapies for presbyopia and myopia. Comparable as an emerging ophthalmic drug-delivery peer targeting similar presbyopia patient population.

TypeBroad incumbent
Description

Major ophthalmic company with broad portfolio across prescription pharmaceuticals, surgical devices, and consumer vision care. Comparable as a broad incumbent selling through the same ECP channel and addressing adjacent vision-correction categories.

TypeDirect peer
Description

Late clinical-stage ophthalmic pharmaceutical company developing therapies for refractive and presbyopia indications. Direct specialty-pharma peer with similar regulatory and commercial pathway targeting ECPs.

TypeRegional player
Description

European-based ophthalmic pharmaceutical company focused on glaucoma and ocular surface disease. Comparable as a specialty ophthalmic pharma peer with similar development focus and ECP channel, though primarily serving European markets.

TypeEmerging player
Description

Clinical-stage ophthalmic company developing reproxalap and other therapies for dry eye and anterior segment conditions. Comparable as an emerging ophthalmic pharmaceutical peer in adjacent therapeutic categories.

TypeBroad incumbent
Description

Ophthalmic pharmaceutical company specializing in glaucoma and retinal diseases; acquired by Alcon. Comparable as a specialty ophthalmic pharma peer developing prescription therapies through the same ECP channel.

TypeEmerging player
Description

Ophthalmic pharmaceutical company developing OC-01 (tyrosine derivative) nasal spray for dry eye; acquired by Viatris. Comparable as an emerging prescription ophthalmic pharma peer commercializing through eye care professionals.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment1 record

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature2 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors5 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Visus Therapeutics

Ophthalmic Pharmaceuticalsvisustx.com

Visus Therapeutics is a clinical-stage ophthalmic pharmaceutical company that developed Yuvezzi, the first FDA-approved fixed-dose combination eye drop for presbyopia. Now an affiliate of Tenpoint Therapeutics following a December 2024 merger, with U.S. commercial launch planned for Q2 2026.

What Visus Therapeutics does

Visus Therapeutics is a clinical-stage ophthalmic pharmaceutical company founded in 2017 and headquartered in Seattle, Washington, that developed Yuvezzi, the first and only FDA-approved fixed-dose combination eye drop for presbyopia. Yuvezzi combines carbachol (a cholinergic agonist) and brimonidine tartrate (an alpha-2 adrenergic agonist) in a single prescription formulation, with Phase 3 trials (536 patients) demonstrating superiority over individual components and a duration of effect of up to 10 hours with no serious adverse effects over 12 months. The company also filed BRIMOCHOL PF (NDA accepted June 2025), a related presbyopia asset within the same chemical family.

In December 2024 Visus merged with Tenpoint Therapeutics Ltd., consolidating pipelines targeting presbyopia, cataracts, and geographic atrophy under a combined entity headquartered at 25 Independence Blvd., Suite 100, Warren, NJ; Visus now operates as an affiliate of Tenpoint. Yuvezzi received FDA approval on January 29, 2026, and is planned for U.S. commercial launch in Q2 2026.

Visus/Tenpoint generates revenue (once launched) through prescription pharmaceutical sales distributed via retail and specialty pharmacies, with prescribing driven through an enterprise field sales motion targeting ophthalmologists and optometrists. The company maintains a dedicated eye care professional portal (yuvezziecp.com) to support prescriber engagement. Pre-launch, the company is pre-revenue; cumulative capital raised totals approximately $235 million, including a $85 million Series B led by Janus Henderson with EQT Nexus, Hillhouse, and the British Business Bank, plus a $150 million debt facility from Hercules Capital. Leadership includes co-founder and CEO Ben Bergo, SVP of Business Development and Marketing Jehan Tamboowalla, and CFO Melissa Epperly.

Visus Therapeutics firmographics

Firmographics
Name
Visus Therapeutics
Legal name
Visus Therapeutics, Inc.
Website
https://visustx.com
Company type
Private
Founded year
2017
Operating status
Operating
Headcount range
11–50 employees
Short description
Visus Therapeutics is a clinical-stage ophthalmic pharmaceutical company that developed Yuvezzi, the first FDA-approved fixed-dose combination eye drop for presbyopia. Now an affiliate of Tenpoint Therapeutics following a December 2024 merger, with U.S. commercial launch planned for Q2 2026.
Ownership category
akta.pro rank

Visus Therapeutics industry classification

Industry
Product category
Ophthalmic Pharmaceuticals
NAICS
Ophthalmic Goods Manufacturing (339115)
SIC
Surgical & Medical Instruments & Apparatus (3841)
akta.pro industry
PRIMARYHLAIACAK
Ophthalmology Specialty Pharmaceuticals
SECONDARYHLAHAIAL
Ocular Drug Delivery Devices (Eye Droppers/Inserts)
Healthcare & Life Sciences/Medical Devices & Diagnostics/Drug Delivery Devices (Injectors, Pumps, Inhalers)

Keywords

  • Presbyopia eye drops
  • Ophthalmic pharmaceuticals
  • Fixed-dose combination
  • Prescription therapeutics
  • Vision restoration

Where Visus Therapeutics is headquartered

Location

Headquarters

HQ city
Seattle
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Visus Therapeutics business model

Business model
GTM type
B2C
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Supply Chain, Marketing or Sales, Operations

Revenue model

  1. Prescription Pharmaceutical Sales: Revenue generated from selling prescription eye drop medications (Yuvezzi) through pharmacies and eye care professionals. Launch planned for Q2 2026 following FDA approval.

Go-to-market motion1 record

Distribution channels2 records

Marketing channels1 record

Visus Therapeutics product offering

Product offering

Core offering

Visus Therapeutics develops prescription ophthalmic pharmaceutical products for age-related vision conditions, principally presbyopia. Its lead product, Yuvezzi, is the first FDA-approved fixed-dose combination eye drop combining carbachol and brimonidine tartrate, offering up to 10 hours of functional near vision improvement. The company is also developing BRIMOCHOL PF, a presbyopia candidate in the same therapeutic class.

Product overview

Visus Therapeutics, a Seattle-based company that merged with Tenpoint Therapeutics, developed Yuvezzi as its lead product. Yuvezzi is a dual-agent combination eye drop (carbachol and brimonidine tartrate) designed to treat presbyopia, an age-related vision condition affecting near focus. The company previously filed for NDA for BRIMOCHOL PF, which appears to be related to or part of the same product family. Following the merger, Tenpoint now handles commercialization of Yuvezzi after receiving FDA approval in January 2026.

Differentiator

Problem solved

Functional benefit

Brands

  • Yuvezzi: Presbyopia eye drop treatment combining carbachol and brimonidine tartrate - the first fixed-dose combination therapy for age-related vision condition affecting approximately 2 billion people globally.

Products and services

  • Yuvezzi Yuvezzi is a prescription dual-agent combination eye drop therapy combining carbachol and brimonidine tartrate, indicated for the treatment of presbyopia (age-related loss of near visual acuity) in adults. It is the first and only fixed-dose combination therapy approved by the FDA for presbyopia, providing up to 10 hours of functional near vision improvement.

Quantifiable outcome

  • Phase 3 trials demonstrated superiority over individual components with no serious adverse effects over 12-month safety study
  • +2 more outcomes

Companies that use Visus Therapeutics

Customer profile

Segments1 record

Ideal customer profiles2 records

Visus Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature2 records

Visus Therapeutics partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Tenpoint TherapeuticsflagshipStrategic or Co-development PartnerVisus Therapeutics merged with Tenpoint Therapeutics in December 2024 to form a combined company focused on ophthalmic medicines. The merger consolidated pipelines targeting presbyopia, cataracts, and geographic atrophy. Yuvezzi originated from Visus and received FDA approval under the combined entity.

Scale indicators4 records

Recent moves6 records

Expansion highlights6 records

Visus Therapeutics competitors and assessment

Company assessment

Broad incumbents

  • Allergan (AbbVie): Markets Vuity (pilocarpine 1.25%), the first FDA-approved presbyopia eye drop. Direct therapeutic competitor to Yuvezzi and a broad ophthalmology incumbent with deep commercial reach and prescriber relationships.
  • Bausch + Lomb: Major ophthalmic company with broad portfolio across prescription pharmaceuticals, surgical devices, and consumer vision care. Comparable as a broad incumbent selling through the same ECP channel and addressing adjacent vision-correction categories.
  • Aerie Pharmaceuticals (Alcon): Ophthalmic pharmaceutical company specializing in glaucoma and retinal diseases; acquired by Alcon. Comparable as a specialty ophthalmic pharma peer developing prescription therapies through the same ECP channel.

Direct peers

  • Lenz Therapeutics: Clinical-stage ophthalmic company developing aceclidine-based presbyopia eye drops (LNZ100/LNZ101). Directly competes with Yuvezzi in the prescription presbyopia drop category with a similar regulatory and commercial pathway.
  • Orasis Pharmaceuticals: Developed Qlosi (pilocarpine 0.4%), an FDA-approved presbyopia eye drop. Directly competes with Yuvezzi in the same ECP prescribing channel and patient population.
  • Ocuphire Pharma: Late clinical-stage ophthalmic pharmaceutical company developing therapies for refractive and presbyopia indications. Direct specialty-pharma peer with similar regulatory and commercial pathway targeting ECPs.

Emerging players

  • Eyenovia: Ophthalmic pharmaceutical company developing microdose array print platform therapies for presbyopia and myopia. Comparable as an emerging ophthalmic drug-delivery peer targeting similar presbyopia patient population.
  • Aldeyra Therapeutics: Clinical-stage ophthalmic company developing reproxalap and other therapies for dry eye and anterior segment conditions. Comparable as an emerging ophthalmic pharmaceutical peer in adjacent therapeutic categories.
  • Oyster Point Pharma (Viatris): Ophthalmic pharmaceutical company developing OC-01 (tyrosine derivative) nasal spray for dry eye; acquired by Viatris. Comparable as an emerging prescription ophthalmic pharma peer commercializing through eye care professionals.

Regional players

  • Nicox Ophthalmics: European-based ophthalmic pharmaceutical company focused on glaucoma and ocular surface disease. Comparable as a specialty ophthalmic pharma peer with similar development focus and ECP channel, though primarily serving European markets.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks5 records

Key highlights6 records

Customer concentration

Visus Therapeutics social profiles

Digital presence

Visus Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Visus Therapeutics leadership team

Management profile

Number of profiles

Profiles3 records

Visus Therapeutics funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors5 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Visus Therapeutics M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Visus Therapeutics

What does Visus Therapeutics do?

Visus Therapeutics develops prescription ophthalmic pharmaceutical products for age-related vision conditions, principally presbyopia. Its lead product, Yuvezzi, is the first FDA-approved fixed-dose combination eye drop combining carbachol and brimonidine tartrate, offering up to 10 hours of functional near vision improvement. The company is also developing BRIMOCHOL PF, a presbyopia candidate in the same therapeutic class.

Is Visus Therapeutics a public or private company?

Visus Therapeutics is a private company. It is classified as venture growth investor backed and is currently operating.

When was Visus Therapeutics founded?

Visus Therapeutics was founded in 2017. It employs 11 to 50 people.

Where is Visus Therapeutics based?

Visus Therapeutics is headquartered in Seattle, United States, in the North America region.

How does Visus Therapeutics make money?

One revenue line is on record: prescription Pharmaceutical Sales.

Who are Visus Therapeutics's main competitors?

Broad incumbents on record are Allergan (AbbVie), Bausch + Lomb and Aerie Pharmaceuticals (Alcon). Direct peers are Lenz Therapeutics, Orasis Pharmaceuticals and Ocuphire Pharma. Emerging players are Eyenovia, Aldeyra Therapeutics and Oyster Point Pharma (Viatris). Nicox Ophthalmics is listed as a regional player.

Does Visus Therapeutics have an API?

No public API is recorded for Visus Therapeutics.

What industry is Visus Therapeutics in?

Visus Therapeutics's product category is Ophthalmic Pharmaceuticals. Its primary akta.pro industry code is HLAIACAK, Ophthalmology Specialty Pharmaceuticals, with a secondary code of HLAHAIAL, Ocular Drug Delivery Devices (Eye Droppers/Inserts). Its NAICS code is 339115 and its SIC code is 3841.

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Live signals
https://www.outlookbusiness.com/Lupin, Tenpoint Therapeutics Enter Into Partnership To Commercialise YUVEZZI – Outlook BusinessLupin Ltd, through its subsidiary VISUfarma BV, has entered into an exclusive licensing agreement with Visus Therapeutics Inc to commercialise the ophthalmic product YUVEZZI in specified European markets. The deal involves a 20 million euro strategic investment in Visus and offers up to 55 million euros in potential milestone payments, bringing the total consideration to 75 million euros.PR NewswireLupin und Tenpoint Therapeutics geben strategische Partnerschaft zur Vermarktung von YUVEZZI™ in der Europäischen Union, dem Vereinigten Königreich, der Schweiz, Norwegen und Island bekanntLupin Limited, through its subsidiary VISUfarma, has entered into an exclusive licensing agreement with Tenpoint Therapeutics to commercialize the presbyopia eye drop YUVEZZI™ in the European Union, UK, Switzerland, Norway, and Iceland. As part of this strategic partnership, VISUfarma will make a strategic investment in Visus Therapeutics, Tenpoint's subsidiary, while retaining rights for regulatory approval and sales in the designated regions.The Times of IndiaLupin arm to commercialise YUVEZZI eye drop across key European marketsLupin Ltd's subsidiary VISUfarma BV has entered into an exclusive licensing agreement with Visus Therapeutics Inc to commercialise the eye drop YUVEZZI in key European markets. The deal involves a 20 million euro strategic investment in Visus and potential milestone payments totaling up to 75 million euros, alongside tiered royalties on net sales.ScanXLupin signs exclusive European deal with Visus for YuveziLupin Limited has secured exclusive rights to commercialize the presbyopia treatment Yuvezi in Europe, the UK, Switzerland, Norway, and Iceland through a licensing agreement with Visus Therapeutics. The deal involves a €20 million strategic investment via a SAFE instrument and up to €55 million in potential milestone payments, totaling €75 million. This partnership aims to strengthen Lupin's ophthalmology portfolio and expand its specialty business presence.The Times of IndiaLupin arm to commercialise YUVEZZI eye drop across key European marketsLupin Ltd announced that its wholly-owned subsidiary VISUfarma BV has entered into an exclusive licensing agreement with Visus Therapeutics Inc to commercialise the ophthalmic product YUVEZZI in specified European markets. The deal involves a total potential consideration of up to 75 million euros, comprising a 20 million euro strategic investment in Visus and up to 55 million euros in regulatory and commercial milestone payments. This partnership aims to strengthen Lupin's vision care franchise by introducing the first approved once-daily dual-agent eye drop for presbyopia to key territories including the EU, UK, Switzerland, Norway, and Iceland.NewswireLupin and Tenpoint Therapeutics Announce Strategic Partnership to Commercialize YUVEZZI™ in the European Union, the United Kingdom, Switzerland, Norway, and IcelandLupin's VISUfarma entered an exclusive licensing agreement with Tenpoint Therapeutics to commercialize YUVEZZI, a once-daily presbyopia eye drop, in the EU, UK, Switzerland, Norway, and Iceland. The deal includes strategic investment, milestone payments, and tiered royalties. Tenpoint is advancing U.S. commercialization and has submitted an MMA in the UK.BioSpaceLupin and Tenpoint Therapeutics Announce Strategic Partnership to Commercialize YUVEZZI™ in the European Union, the United Kingdom, Switzerland, Norway, and IcelandLupin's VISUfarma entered an exclusive licensing agreement with Tenpoint Therapeutics to commercialize YUVEZZI in the EU, UK, Switzerland, Norway, and Iceland. VISUfarma will invest in Visus, and both parties will receive milestone payments and tiered royalties. Tenpoint is advancing U.S. commercialization after FDA approval.https://www.outlookbusiness.com/Lupin, Tenpoint Therapeutics Enter Into Partnership To Commercialise YUVEZZI – Outlook BusinessLupin Ltd's wholly-owned subsidiary VISUfarma BV has entered into an exclusive licensing agreement with Visus Therapeutics Inc to commercialize the ophthalmic product YUVEZZI in specified European markets. The partnership involves a strategic investment and offers up to 75 million euros in potential regulatory and commercial milestone payments through first sales. This deal aims to strengthen Lupin's vision care franchise and expand its presence in key European territories including the EU, UK, Switzerland, Norway, and Iceland.FiercePharmaTenpoint scores FDA nod for vision-correction eye drop Yuvezzi, plans Q2 launch with $235M in towLondon-based Tenpoint Therapeutics received FDA approval for Yuvezzi, a combination eye drop treatment for presbyopia that combines carbachol and brimonidine tartrate, becoming the first fixed-dose combination therapy for the age-related vision condition affecting roughly 2 billion people globally and 128 million in the United States. The company raised an $85 million Series B round led by Janus Henderson, EQT Nexus, Hillhouse, and the British Business Bank, and secured a $150 million debt facility from Hercules Capital, totaling $235 million to fund the product's launch planned for early Q2. Yuvezzi originated from Visus Therapeutics, a Seattle-based company that merged with Tenpoint 13 months ago, and the approval was backed by Phase 3 trials demonstrating superiority over individual components with no serious adverse effects over a 12-month safety study.Eyes On EyecareTenpoint and Visus Therapeutics merge with plans for ophthalmic therapeutic advancementsTenpoint Therapeutics, Limited and Visus Therapeutics, Inc. have completed their merger to focus on developing ophthalmic therapeutic medicines aimed at rejuvenating the aging eye. The newly-merged company will operate under the Tenpoint name, with plans to file a new drug application for their lead asset, BRIMOCHOL PF, in the first half of 2025 and a tentative U.S. commercial launch by mid-2026. This merger aligns with the companies' efforts to advance innovative treatments for age-related vision loss and other ocular diseases.