Adding Life to Medicines

We bring new perspectives to approved medicines, unlocking new possibilities and applications.

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Our Mission

Uncover New Possibilities for Approved Drugs

Revio’s mission is to pivot approved medicines towards new indications or optimize its use within existing indications via improved delivery and product features.

Our approach creates opportunities to leverage novel biology around proven medicines, explore new indications, innovative dosage forms, delivery systems, combinations and new routes of administration.
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We aim to accelerate drug development, reduce risk of failures, and deliver better outcomes for patients while creating meaningful value for all stakeholders.

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Who We Are
Revio are the drug innovators.

We are expert drug developers.

With years of experience in successful regulatory approvals, global & regional licensing deals, and new product launches across therapeutic areas, we know how to make a molecule market-ready. 

We develop drugs with optimized processes, efficient timelines, and better outcomes.

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What We Do
Revio develops drugs for rare diseases.

Drug development is expensive, risky, and time-consuming.

New drug candidates often fail in development or are approved with sub-optimal labels due to safety concerns.

Approved drugs have an established safety record.
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At Revio, we seek to uncover new possibilities for approved drugs, which can lead to more efficient drug development, positively impacting all stakeholders.

John Carter Avatar Circle Image - Laboratory X Webflow Template
John Carter
Principal scientist
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Drug development is expensive, risky, and time-consuming.

New drug candidates often fail in early-stage clinical trials due to safety concerns. 
Approved drugs have an established track record of safety.

Our Strengths
01

Efficient drug development

Working with proven medicines to save time & money by shortening the development path and cycle times

02

Reduced development risk

Reducing the risk of failure by leveraging existing safety data of approved drugs and employing translational approaches to uncover new indications

03

Better patient outcomes

Unlocking the full potential of approved drugs by optimizing drug delivery & product features.

Our Business Model

We believe strong partnerships & efficient structuring are critical to tackling the complexity of drug development.

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We believe strong partnerships & efficient structuring are critical to resolving the complexity of drug development.

01

Early-Stage Collaboration

We work with academic researchers and biotech innovators to transform early-stage ideas into clinical realities. From licensing intellectual property to co-developing assets, we ensure every step is efficient and impactful.

02

Late-Stage Licensing

Partnering with large pharma companies, we take assets through final development and commercialization with precision

03

Hub-and-Spoke Model

With a central team overseeing strategy and execution, our lean & nimble corporate structure enables allows focus on  individual assets for streamlined development and monetization.

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Rare Indications

Why Rare Diseases?

These conditions may affect fewer people, but their impact is profound.

By focusing on rare diseases and niche therapeutic areas, we dedicate our expertise to creating breakthrough solutions for patients who need them most.

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01

Unmet Needs

With over 7,000 known rare diseases, 95% lack FDA-approved treatments. We aim to close this gap.

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Smarter Development

Rare disease research benefits from regulatory incentives and the voices of empowered patient communities.

Therapeutics Areas

Our Therapeutics Areas 

We seek to uncover new possibilities for approved drugs, specifically in rare diseases & niche indications.

Muscular Dystrophy

Collaborating on an approved DMD molecule using AI-enabled approaches to explore potential applications across multiple dystrophinopathies.

Glioblastoma

Partnering with nanotechnology experts, we’re developing an innovative intra-tumoral formulation to enhance efficacy while minimizing side effects.

Other Assets & Indications

Exploring treatments for neurological diseases and antimicrobial resistance (AMR).

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Therapeutics Areas

High cellular toxicity is a common problem with oncology drugs. In partnership with a major pharma company, Revio is co-developing a new drug combination with lower cytotoxicity and novel route of delivery for glioblastoma. 

Muscular Dystrophy

Muscle weakness and loss of muscle mass are typical symptoms of muscular dystrophy. The root cause of the condition is genetic and has no approved medications.

Revio is working with a startup with expertise in artificial intelligence and developing a new application for a drug that is approved for the management of diabetes.

Glioblastoma

High cellular toxicity is a common problem with oncology drugs. In partnership with a major pharma company, Revio is co-developing a new drug combination with lower cytotoxicity and novel route of delivery for glioblastoma. 

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News and Media

News and Media

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Revio Therapeutics Announces Licensing Agreement with Peptris Technologies & Poster Presentation at the 2025 Muscular Dystrophy Association Conference

Revio Therapeutics Announces Licensing Agreement with Peptris Technologies & Poster Presentation at the 2025 Muscular Dystrophy Association Conference

Revio Therapeutics, a privately held specialty pharma start-up focused on repurposing & optimizing approved medicines...

March 17, 2025
Press Articles
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At Revio we have the passion & expertise to develop successful drugs that improve patients’ lives & create value for all stakeholders. And we value partnerships that are mutually accretive and help us succeed in our mission.

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For Researchers

Have an idea or IP ready for development? Partner with us to turn it into a reality.

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For Pharmaceutical and Biotech Companies

Let’s join forces to bring cutting-edge programs to the finish line.

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For Investors

Be part of our mission to revolutionize drug development and deliver measurable impact.

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