Chroma Medicine

About Chroma Medicine

Chroma Medicine is developing epigenetic editing technologies that modify chromatin structure to precisely regulate gene expression without altering the DNA sequence. This approach aims to create durable genomic therapies for diseases that currently lack effective treatments.

```xml <problem> Many diseases lack effective treatments due to the limitations of traditional gene therapies that permanently alter the DNA sequence. These methods can lead to unintended consequences and are not suitable for conditions requiring precise and reversible gene regulation. </problem> <solution> Chroma Medicine is developing epigenetic editing technologies that modify chromatin structure to precisely regulate gene expression without altering the underlying DNA sequence. This approach allows for durable yet reversible control over gene activity, offering a new class of genomic medicines. By harnessing the power of epigenetics, Chroma aims to create therapies that can precisely control gene expression, leading to more effective and safer treatments for a wide range of diseases. This innovative approach promises unparalleled control of gene expression, addressing the limitations of existing gene therapies. </solution> <features> - Epigenetic editing technology that modifies chromatin structure. - Precise regulation of gene expression without altering the DNA sequence. - Durable and reversible control over gene activity. </features> <target_audience> Chroma Medicine's primary focus is on patients suffering from diseases that currently lack effective treatments and can benefit from precise and durable gene regulation. </target_audience> ```

What does Chroma Medicine do?

Chroma Medicine is developing epigenetic editing technologies that modify chromatin structure to precisely regulate gene expression without altering the DNA sequence. This approach aims to create durable genomic therapies for diseases that currently lack effective treatments.

Where is Chroma Medicine located?

Chroma Medicine is based in Cambridge, United Kingdom.

When was Chroma Medicine founded?

Chroma Medicine was founded in 2021.

How much funding has Chroma Medicine raised?

Chroma Medicine has raised 135000000.

Location
Cambridge, United Kingdom
Founded
2021
Funding
135000000
Employees
55 employees
Major Investors
Google Ventures

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Chroma Medicine

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Executive Summary

Chroma Medicine is developing epigenetic editing technologies that modify chromatin structure to precisely regulate gene expression without altering the DNA sequence. This approach aims to create durable genomic therapies for diseases that currently lack effective treatments.

chromamedicine.com7K+
cb
Crunchbase
Founded 2021Cambridge, United Kingdom

Funding

$

Estimated Funding

$100M+

Major Investors

Google Ventures

Team (50+)

No team information available.

Company Description

Problem

Many diseases lack effective treatments due to the limitations of traditional gene therapies that permanently alter the DNA sequence. These methods can lead to unintended consequences and are not suitable for conditions requiring precise and reversible gene regulation.

Solution

Chroma Medicine is developing epigenetic editing technologies that modify chromatin structure to precisely regulate gene expression without altering the underlying DNA sequence. This approach allows for durable yet reversible control over gene activity, offering a new class of genomic medicines. By harnessing the power of epigenetics, Chroma aims to create therapies that can precisely control gene expression, leading to more effective and safer treatments for a wide range of diseases. This innovative approach promises unparalleled control of gene expression, addressing the limitations of existing gene therapies.

Features

Epigenetic editing technology that modifies chromatin structure.

Precise regulation of gene expression without altering the DNA sequence.

Durable and reversible control over gene activity.

Target Audience

Chroma Medicine's primary focus is on patients suffering from diseases that currently lack effective treatments and can benefit from precise and durable gene regulation.

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