Integra Therapeutics

About Integra Therapeutics

Integra Therapeutics develops gene writing tools that combine CRISPR-Cas precision with engineered piggybac transposase for efficient delivery of both small and large DNA payloads. The technology addresses limitations in gene therapy related to gene size, precision, and stability, aiming to cure genetic and oncological diseases with high unmet medical needs.

```xml <problem> Current gene therapies face limitations in delivering large genetic payloads, achieving precise gene editing, and ensuring long-term therapeutic stability, hindering their effectiveness in treating genetic and oncological diseases. These challenges restrict the scope of treatable conditions and necessitate improved gene writing tools. </problem> <solution> Integra Therapeutics is developing advanced gene writing tools that combine the precision of CRISPR-Cas technology with an engineered piggybac transposase. This platform, called FiCAT, enables efficient delivery of both small and large DNA payloads, overcoming size constraints in gene therapy. By integrating CRISPR-Cas for targeted editing and piggybac transposase for efficient gene transfer, Integra aims to enhance the scope, efficiency, and safety of advanced therapies. The technology seeks to provide more precise and stable gene modifications, ultimately improving the treatment of genetic and oncological diseases with high unmet medical needs. </solution> <features> - FiCAT platform combines CRISPR-Cas precision with piggybac transposase efficiency. - Enables delivery of both small and large DNA payloads. - Aims to improve the scope, efficiency, and safety of advanced therapies. - Designed for precise and stable gene modifications. </features> <target_audience> The primary target audience includes researchers and clinicians in the fields of gene therapy, oncology, and genetic diseases seeking advanced tools for precise and efficient gene editing and delivery. </target_audience> ```

What does Integra Therapeutics do?

Integra Therapeutics develops gene writing tools that combine CRISPR-Cas precision with engineered piggybac transposase for efficient delivery of both small and large DNA payloads. The technology addresses limitations in gene therapy related to gene size, precision, and stability, aiming to cure genetic and oncological diseases with high unmet medical needs.

Where is Integra Therapeutics located?

Integra Therapeutics is based in Barcelona, Spain.

How much funding has Integra Therapeutics raised?

Integra Therapeutics has raised 6780000.

Location
Barcelona, Spain
Funding
6780000
Employees
21 employees
Major Investors
EIC Accelerator

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Integra Therapeutics

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Executive Summary

Integra Therapeutics develops gene writing tools that combine CRISPR-Cas precision with engineered piggybac transposase for efficient delivery of both small and large DNA payloads. The technology addresses limitations in gene therapy related to gene size, precision, and stability, aiming to cure genetic and oncological diseases with high unmet medical needs.

Funding

$

Estimated Funding

$5M+

Major Investors

EIC Accelerator

Team (20+)

No team information available.

Company Description

Problem

Current gene therapies face limitations in delivering large genetic payloads, achieving precise gene editing, and ensuring long-term therapeutic stability, hindering their effectiveness in treating genetic and oncological diseases. These challenges restrict the scope of treatable conditions and necessitate improved gene writing tools.

Solution

Integra Therapeutics is developing advanced gene writing tools that combine the precision of CRISPR-Cas technology with an engineered piggybac transposase. This platform, called FiCAT, enables efficient delivery of both small and large DNA payloads, overcoming size constraints in gene therapy. By integrating CRISPR-Cas for targeted editing and piggybac transposase for efficient gene transfer, Integra aims to enhance the scope, efficiency, and safety of advanced therapies. The technology seeks to provide more precise and stable gene modifications, ultimately improving the treatment of genetic and oncological diseases with high unmet medical needs.

Features

FiCAT platform combines CRISPR-Cas precision with piggybac transposase efficiency.

Enables delivery of both small and large DNA payloads.

Aims to improve the scope, efficiency, and safety of advanced therapies.

Designed for precise and stable gene modifications.

Target Audience

The primary target audience includes researchers and clinicians in the fields of gene therapy, oncology, and genetic diseases seeking advanced tools for precise and efficient gene editing and delivery.

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