Applied Clinical Trials: When is it Time to Kill Your Drug?

July 27, 2018

It can be hard for drug makers to pull the plug on a drug in development, even when all signs indicate they should – resulting in many drugs getting past the preclinical floodgates, only to fail. The mistake: Not having a clinical strategy from the get-go.

A smart, defined clinical strategy sets objective expectations at the beginning of a drug’s development for when and on what criteria development will be terminated. This forces drug developers to ask, “Why are we creating this drug in the first place?”

The answer—and the true drug development opportunity—lies in an understanding of the best available science and patient target(s) for the drug.

Before you take your drug to the point of no return, learn more about TD2’s insight from president and CEO, Stephen Gately, on how to be more strategic from the start in Applied Clinical Trials.

The Importance of Conducting PDX Oncology Studies in a Humanized Immune System

Preclinical oncology studies are a critical step in developing effective cancer therapies. Patient-derived xenograft (PDX) models have become a ...

Read more +

Leveraging Flow Cytometry to Drive Better Patient Outcomes in Hematologic Malignancy Clinical Trials

In oncology, evaluating treatment efficacy often relies on standardized criteria such as RECIST (Response Evaluation Criteria in Solid Tumors), which ...

Read more +

The Importance of Incorporating Metabolomic and Proteomic Screening in Preclinical Oncology Studies

The evolving complexity of oncology drug development demands an equally sophisticated approach to understanding the tumor microenvironment and its ...

Read more +

Get Started

Contact Us Today!

If you’re looking for an expert team to guide your trial with efficiency in mind, we can help. As the creators of the Dynamic Trial, TD2 provides start-to-finish support with trial strategy, design and execution for faster go-to-market potential.