About

The Institute of Molecular Medicine at Phoenix Children's Hospital

Molecules and DNA strands

Molecular, or personalized, medicine uses genetic information to determine the right treatment for the right patient at the right time.

By studying a patient's genetic makeup, researchers can identify their susceptibility to disease, predict their response to a particular drug and match the patient with a personalized therapy.

Challenges with existing molecular medicine programs include:

  • The amount of time that it takes to develop a new drug or treatment.
  • 70 percent of all medications prescribed to children have been tested only in adults.  (Clinical studies in children lead to a better understanding of the specific differences between children and adults, thus leading to the development of safer, more effective and age-appropriate treatments.)
  • Research and development of novel treatments for pediatric diseases have fallen short over past decades. 

New collaboration brings new hope to children

molecular medicine logo

Phoenix Children’s Hospital announced the creation of the Institute of Molecular Medicine on Dec. 4, 2012, with the goal to unlock genetic codes and develop drug therapies to improve the outcome for thousands of young patients.

A founding gift by Ronald A. Matricaria provided the initial investment to establish the Institute. Matricaria is a member of the Phoenix Children’s Hospital board of directors and former chairman/CEO of St. Jude Medical, Inc. Additional funding for the $50 million venture will come from philanthropic contributions and grant revenue.

A critical component to this venture is Phoenix Children’s collaborative relationships with leading bioscience institutions.

The Institute is a critical piece in the development Phoenix Children's emerging academic medical program and will position the Hospital to become national contributors and leaders in molecular medicine.

Additional information and resources

Learn about pediatric cancers.

Read the full press release.

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