Early Clinical Development / Phase IIa

An experienced partner gets you results as you introduce your compound in humans and move to proof of concept.

  • Your clinical pharmacology team brings over 30 years of direct drug development experience

  • Your partners include over 250 staff fully dedicated to early patient studies

  • Optimize your early patient studies with over 300 investigator sites around the globe

Your Needs

Study delays and missed recruitment timelines are far too common. Your main considerations are quality, time and cost. By partnering with Covance, you can rest assured that your drug will stay on track toward the next development milestone. Our processes are specifically designed for early clinical studies. In fact, we have locked over 1,000 databases and met our healthy volunteer and patient enrollments over 90% in the past 5 years.

You only need access to the resources that matter most to your study and you shouldn’t have to deal with a bigger footprint than you need. We understand. That’s why we deliver the right combination of strategy and execution, resources and tools that help you meet your end goals.

You want a team of experts that have a proven track record in your therapeutic area. We deliver recognized thought leaders in early clinical design and execution for a variety of therapeutic indications including oncology, metabolic, neuroscience, cardiovascular, inflammation and infectious disease.

Our Capabilities

We offer you a deep, experienced team focused on this crucial phase of molecule development. Let us partner with you as you transition into the clinic with an eye toward future phases.