Technology licensing and industry partnerships

OSAP is the business development and licensing engine of the Broad and welcomes opportunities to explore new partnerships and ventures with industry. Our goal is to close the gap between discoveries at Broad and benefits for patients through close collaborations and licensing agreements with industry partners.

Broad’s unique institutional structure enables partnerships that span multiple investigators and scalable platform technologies across a variety of research areas.

Please contact us at partnering@broadinstitute.org

Technology licensing and new ventures

Here are a few examples of how Broad has successfully partnered with industry to drive impact in human health and research:

These clinical-stage companies were founded with exclusive licenses to Broad-developed gene editing technologies for therapeutic applications:

  • Beam Therapeutics: testing several base-editing treatments in clinical trials for genetic diseases 
  • Editas Medicine: testing CRISPR-Cas9/Cas12a-based treatments. Editas has exclusive licences to these CRISPR technologies from Broad for human medicines, which enabled Casgevy, the first FDA-approved CRISPR medicine. 
  • Prime Medicine: testing several prime editors in preclinical work and an early-stage clinical trial for genetic diseases and cancer
A conceptual 3D illustration of prime editing, showing a molecular machine (Cas9 and reverse transcriptase) interacting with a DNA double helix to 'search and replace' a specific genetic sequence.

These companies launched with licensing agreements with Broad to build new approaches to delivering genetic medicines to targeted cells and tissues in the body: 

  • Aera Therapeutics: a delivery-focused genetic medicine company focusing on nanoparticles and other approaches
  • Apertura Gene Therapy: advancing AAVs for genetic medicines for central nervous system and neuromuscular diseases
  • Kate Therapeutics: developing AAV-based genetic medicines for neuromuscular disorders. Acquired by Novartis.
3D model of adeno-associated viruses.

Here are examples of companies that are commercializing research technologies developed at Broad, scaling them up and lowering costs to help advance science everywhere. 

Bifrost Biosystems signed an exclusive licensing agreement with Broad in 2024 to gain access to optical pooled screening, a Broad-developed technology that connects single-cell phenotype to genotype at massive scale. 

Curio Bioscience launched in 2023 to commercialize high-resolution and single-cell spatial mapping tools developed at Broad. Acquired by Takara Bio USA.

In situ sequencing identifies the gene knockout in each cell of a pooled CRISPR library. Fluorescence microscopy records both cellular phenotypes and sequencing data (cell nuclei are depicted in gray and the nucleotide bases are green = guanine, red = thymine, magenta = adenine and cyan = cytosine).

Broad grants non-exclusive licenses to gene editing technologies for academic/research and agricultural use. Learn more here.

Conceptual illustration of CRISPR-Cas9 system by Stephen Dixon.

Broad partnered with Manifold, a leader in research infrastructure for biomedical science, to develop a cutting-edge research platform. The platform builds on the principles of Terra, a trusted system for large-scale data analysis and secure collaboration. 

Broad also collaborated with Illumina to integrate GATK — a genome-analysis tool created by Broad scientists — with Illumina’s DRAGEN tool for genomic data analysis.

Terra logo

Research collaborations

Through longstanding partnerships, Broad and industry scientists work closely together to make new discoveries and move them toward clinical application. Some examples of our strategic research collaborations include:

Broad-Bayer alliances launched in 2013 for oncology and in 2015 for cardiovascular research. The oncology alliance has led to a lung cancer drug, Hyrnuo®, which received FDA accelerated approval in 2025. The cardiovascular partnership has resulted in an atrial fibrillation drug candidate in early-stage clinical testing.

Drug SEVABERTINIB

Broad and Calico began their partnership in 2015 focused on diseases of aging. It has resulted in a cancer immunotherapy candidate now being tested in an early-stage clinical trial.

Protein diagram showing the new small molecule inhibitor nestled inside the PTPN2 protein.

In 2017, Broad and Deerfield Management began a partnership focused on early-stage academic and therapeutics research. In 2019, Jaguar Gene Therapy launched with financing from Deerfield and a pipeline of gene therapy candidates, including JAG201 for a leading monogenic cause of autism, which is clinically diagnosed as Phelan-McDermid syndrome and is caused by pathogenic variants in the SHANK3 gene or from chromosome 22q13.3 deletions encompassing SHANK3This gene therapy candidate is exclusively licensed from Broad. JAG201 is currently in an early-stage clinical trial.

Scientific illustration of the Shank3 protein and its role in genetic brain disorders.

A joint cancer research collaboration between Microsoft and Broad called Project Ex Vivo envisions a new, constructionist paradigm for precision oncology, one powered by the bottom-up integration of experimentation and computation.

Scientist working in a lab

Broad leads or is a key partner in cutting-edge consortia with industry collaborators, including the Cancer Dependency Map Consortium, which launched in 2018 and has 22 biopharma partners.

Depmap logo

Photo of Todd Golub

photo of Michael Christiano