OVERVIEW

Anticipating human responses to treatment early in drug development is crucial for improving R&D efficiency. By using HUB Organoid Technology, we helped our client evaluate the safety profile of a bispecific T cell engager through organoid and T cell co-cultures derived from both normal and tumor tissues, providing critical insights into on- and off-target toxicity and therapeutic window.

THE CHALLENGE

THE CHALLENGE

Our client needed to assess the safety profile of a bispecific T cell engager. While they had gathered some information from cell lines and animal studies, they needed more accurate, human-relevant data to better understand the tumor-associated antigen (TAA) expression in real patient tissues and its potential effects in normal non-cancerous cells. This was crucial for assessing the safety and efficacy of their bispecific T cell engager in a more clinically predictive context.

THE STRATEGY

THE STRATEGY

To provide a more clinically predictive safety profile, we utilized organoid and T cell co-cultures derived from both normal and tumor tissues from the same patient. This approach allowed us to simulate a human-relevant environment, offering a clear comparison of how the bispecific T cell engager impacted both cancerous and non-cancerous cells. By examining tumor-associated antigen (TAA) expression across matched healthy and diseased tissues, we were able to pinpoint on-target activity while assessing any potential off-target toxicity.

Here is what our clients have to say

Replicating a true tumor microenvironment is complex, yet the organoid and T cell co-culture system offered an invaluable, human-relevant model. It gave us insights that traditional models couldn’t, helping us predict how our therapeutic might behave in actual patient tissues.
– Senior Investigator, Oncology, Pharma*
*anonymized to protect the confidentiality of the client

THE RESULTS

The sample data demonstrated distinct interactions between the bispecific T cell engager and TAA expression in normal versus tumor-derived organoid co-cultures. The results provided critical insights into how the compound engaged T cells in tumor tissues while minimizing effects on healthy cells. Armed with this patient-relevant data, the client was able to refine the therapeutic window, moving forward with a clearer understanding of the compound’s safety and efficacy profile.

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