Flourishing innovation, towards patients' renascence

Recode, new life

Reforgene Medicine develops gene editing therapies for genetic diseases and diseases with major unmet need.

About Reforgene

Curative answers, starting at the genome

Reforgene Medicine is one of China’s leading innovative gene editing drug companies, driven by gene editing technology and dedicated to bringing novel medicines to life.

The company has pipeline programs in genetic diseases and complex diseases. Its innovative beta-thalassemia medicine has achieved globally leading clinical progress, and it achieved the world’s first cure of an alpha-thalassemia patient.

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Reforgene research team
How it works

How gene editing becomes a cure

Rewriting a disease-causing gene at the genome level is the path to a one-time, curative gene editing medicine.

Pinpoint the target gene 01

Pinpoint the target gene

The TIPBAIG™ platform combines genomics and AI to discover and validate targets, tracing disease to a specific gene.

Edit with precision 02

Edit with precision

CRISPR/Cas systems, such as base editors, make precise changes at specified sites. Editing can be performed ex vivo or delivered in vivo using LNP or AAV.

One-time cure 03

One-time cure

Corrected cells restore normal function, enabling a one-time administration with long-term or even lifelong benefit.

Technology Platforms

Three Platforms, One System

An end-to-end system for gene editing drug development, from tool discovery and target identification to safety assessment.

TIPBAIG™
TIPBAIG™

Digital drug development platform

Combining AI, informatics and genomics, TIPBAIG™ accelerates gene editing therapy development from tool engineering to safety assessment.

PGET™
PGET™

Gene editing technology platform

Integrating CRISPR/Cas systems, base editors and novel LNP delivery tools.

GETM™
GETM™

Product platform

Spanning ex vivo cell engineering and in vivo delivery.