Our Story

Guided by Our Founders’ Intent

Staying true to our roots in Kansas City, Missouri, we are guided exclusively by our founders’ intent of hope for life as we focus on translational and clinical efforts in areas of significant unmet need with as broad a scope as possible.

Learn about our story, our founders, and their vision

Our Model

Our Novel Model to Make a Difference

Our uniqueness starts with our funding model. The Stowers Group of Companies receives stable and sustainable resources through private institutional funding via American Century Investments, an asset management firm. The Stowers Group of Companies includes the non-profit Stowers Institute for Medical Research (Stowers Institute), and the for-profit Biomed Valley Discoveries, Inc. (BVD), which is wholly owned by a supporting organization of Stowers Institute. Our founders’ original directive that any profits would accrue to Stowers Institute’s benefit promotes a perpetual, virtuous cycle of scientific innovation and translation to advance breakthrough medicines.

pixels

Biotech,
Purposefully
Reimagined

Our secure funding, in turn, has freed us to break the mold and create a purposefully reimagined approach to every aspect of our business, our pursuit of groundbreaking medicines, and our commitment to patients.

nodelete

Risk-Tolerant Candidate Sourcing

We are empowered to pursue early development assets that are often higher risk but high opportunity for patients that may not fit within the investment profile of traditional industry or investor firms.

nodelete

Deep, Data-Led Scientific Interrogation

We bring a deep level of scientific rigor to de-risking programs, working diligently to deliver focused data that supports whether a program or direction shows promise to address the target unmet need.

nodelete

Extensive Collaborator Network

We focus on early-stage development through clinical proof-of-concept. Our extensive network of physician research collaborators and centers of excellence serve as true partners in our development efforts.

nodelete

Lean, Flexible Corporate Infrastructure

Based in Kansas City, we minimize infrastructure and overhead, operating primarily as a remote team while leveraging a large external network. We are able to deploy resources in a stage-appropriate, prioritized and real-time manner to meet the scientific needs of each program.

nodelete

Unmet Need-Focused Clinical Exploration

We leverage a myriad of clinical activities – BVD-sponsored and investigator-initiated trials, and compassionate use and expanded access programs – to seek early signals and stay focused on the unmet patient need.

nodelete

Partner/Out-Licensing Centric

Once we have de-risked candidates, we seek partners with infrastructure and expertise more suited for the next stage of development to the broadest range of potential indications to carry the asset forward to commercialization.

Our Programs

Breakthrough
Science to Address
Unmet Medical Needs

The common thread across our programs is novel science and biology with the potential to address significant unmet needs in cancer and other serious conditions and deliver on our founders’ intent of hope for life.

Ulixertinib (BVD-523)
PHASE 2 ONGOING

Highly selective, first-in-class ERK 1/2 inhibitor designed to block the terminal node of the MAPK pathway

Learn more about ulixertinib

TEM8/ANTXR1 Therapeutic Antibodies
Preclinical

Harnessing an over-expressed protein in the tumor microenvironment as a lamp post to guide novel antibody-drug conjugates (ADCs)

Learn more about TEM8/ANTXR1

Clostridium novyi-NT (CNV-NT/BVD-550)
Phase 1 Completed

Revitalizing the promise of bacteria to target tumors’ necrotic core and destroy tumors from the inside out

Learn more about CNV-NT

DID YOU KNOW?

Thousands of people are impacted by MAPK pathway-driven cancers. Many of these cancers become resistant to treatment, with the pathway becoming reactivated despite an upstream inhibitor. We believe ERK inhibition is a critical and untapped strategy to address MAPK pathway cancers. Since ERK occupies the last node in the pathway, and many of the resistance mechanisms still rely on ERK signaling to drive disease, a tolerable and effective ERK inhibitor represents an important strategy for the treatment of MAPK pathway-driven cancers.

Learn more about our work in ERK inhibition

What’s New?

The first patient has been dosed in a Phase 2 study of ulixertinib, our highly selective, first-in-class ERK 1/2 inhibitor, in individuals with histiocytosis who have progressed on or cannot tolerate other therapies. This investigator-initiated trial was initiated following the observation of durable efficacy signals in multiple histiocytosis patients who were administered ulixertinib under BVD’s compassionate use program.

Learn more about the study