Current Environment:

Our unique approach to pediatric gene therapy

The Boston Children's Hospital Gene Therapy Program is an international leader in gene therapy with one of the largest pediatric gene therapy programs in the world. Founded in 2010, our success is a result of our program’s clinical expertise, pioneering gene therapy research, and commitment to caring for rare and difficult-to-treat conditions.

What makes us unique is our dedicated infrastructure. Our core team collaborates closely with disease experts at two of the world's leading academic medical institutions — Boston Children’s Hospital and Dana-Farber Cancer Institute. Our efficient enrollment processes allow children to move smoothly and quickly from study enrollment to treatment. We also offer a one-of-a-kind satellite training module to support referring physicians.
 

Illustration: Scissors cutting genes

What is gene therapy?

Read about the different types of gene therapy and how they work.

We have launched and participated in numerous clinical gene therapy trials together with the Dana-Farber/Boston Children’s Cancer and Blood Disorders Center. We also work closely with Boston Children’s Departments of Ophthalmology, Neurology, Neurosurgery, and Pulmonary Medicine; Division of Genetics and Genomics; and Metabolism Program, as well as academic and pharmaceutical partners in the U.S. and abroad. We are a founding member of the Transatlantic Gene Therapy Consortium (TAGTC), which seeks to combine the expertise from a number of centers treating rare diseases with different platforms.

Below are some conditions we are currently treating with gene therapy or for which we plan to offer gene therapy in the near future. Some of these are currently being tested in clinical trials, and some have received approval from the U.S. Food and Drug Administration.

Ongoing gene therapy research

Gene therapy represents a major shift in medicine, offering cures for conditions not previously treatable and for diseases often demanding heroic efforts. Since our founding in 2010, we have treated more than 70 patients from 20 countries through more than 19 gene therapy clinical trials.

.

After decades of evolution, gene therapy arrives

Despite its early checkered history, gene therapy is now becoming a standard of care.

As gene therapy continues to evolve and improve, our team is optimistically embracing new gene-correction technologies such as gene editing, base editing, and gene silencing and conducting active research to make these techniques ever more precise and safe. We feel fortunate to be at the forefront of this field with our patients and families providing motivation and purpose.

Watch: Because of gene therapy

Paul

 

Matthew

 

Harry

 

Our stories

Hemophilia A

Meet Daxton

Chronic Granulomatous Disease

Meet Brenden

Acute Lymphoblastic Leukemia

Meet Ava

Sickle Cell Disease

Meet Manny

Spinal Muscular Atrophy

Meet Sofie

Severe Combined Immunodeficiency

Meet Paul

Adrenoleukodystrophy

Meet Brandon and Brian

Wiskott-Aldrich Syndrome

Meet Emir