About Corlexia

Clinical Trial Operations Experts

Corlexia was created by a team of biotech and pharmaceutical professionals. We even remember the days of three-part paper CRFs. The CRAs would sit and separate the pages, then mail them to data management. That sounds archaic now, and at the time, it seemed EDC would never work. I’m sure we are all glad that EDC replaced our old blue ink pens, and those days of data entry are behind us. The pharmaceutical industry is often in a mode of change, yet the reality is much has stayed the same. One significant challenge is site selection, recruitment, and the high costs of project management during long enrollment periods. 

Corlexia was founded out of need. We were frustrated with low recruitment rates. The standard process of site feasibility hasn’t changed much in the past 30 years, yet the cost of research is steadily rising. Large institutions have high fees,  and the worst part is often they don’t deliver on promised enrollment targets. Meanwhile, many patients do not have access to cutting-edge treatments. We surveyed hundreds of private practice doctors to learn they were interested in adding clinical research trials to their practices.

Corlexia is a mix of former pharmaceutical directors and scientists with backgrounds from pre-clinical toxicology to Phase IV clinical trials. Some have worked for large pharmaceutical companies, and some preferred smaller start-ups. We know how to run studies and develop drugs, and we decided to focus our efforts on finding ways to expedite enrollment. We have experienced firsthand how recruitment rates can end a promising compound. We remove the hurdles so more treatments can be available to more patients and reach the market quicker.

The Corlexia team shares the common belief that Clinical Research studies should be more accessible to more patients. It helps patients, doctors, and drug developers. We know the hurdles, and we’re creating solutions to get better medications to more people quicker.

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