Wicker, Reed Lead Call for Improved Data on Child Participation in NIH Clinical Health Trials

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Wicker, Reed Lead Call for Improved Data on Child Participation in NIH Clinical Health Trials

26 U.S. Senators urge NIH to improve data collection on children participating in clinical health trials

WASHINGTON – U.S. Senators Roger Wicker, R-Miss., and Jack Reed, D-R.I., today sent a letter with 24 of their Senate colleagues urging the National Institutes of Health (NIH) to improve data collection on children participating in NIH-funded clinical health trials.

NIH policy currently requires the inclusion of children in NIH-sponsored clinical trials unless there is reason to exclude them. However, NIH is not systematically tracking the ages of the children included in all of its clinical trials relevant to child health. This lack of data makes it difficult to determine whether children as a whole, or particular pediatric subpopulations, are underrepresented in federally-funded biomedical research. It also makes it difficult to determine how different pediatric subpopulations fare in these trials.

“The United States remains a global leader in biomedical innovations because of groundbreaking NIH research,” Senator Wicker said. “Medical research is instrumental to answering some of the toughest questions of our time. Understanding how new therapies and treatments impact children could prove to be invaluable. Improved data collection and transparency by NIH would be an important step toward ensuring that children benefit from scientific advances funded by the federal government.”

“Clinical research is critically important to our children’s health and NIH must improve its data collection process to allow children to reap the benefits of important scientific advancements,” said Senator Reed. “We need to ensure there is an appropriate amount of pediatric representation in these essential clinical trials so we can ensure there are effective treatments for children down the line.”

In addition to Senators Wicker and Reed, the letter was signed by U.S. Senators Casey (D-PA), Markey (D-MA), Capito (R-WV), Sullivan (R-AK), Coons (D-DE), Ayotte (R-NH), Gillibrand (D-NY), Murphy (D-CT), Stabenow (D-MI), Warren (D-MA), Durbin (D-IL), Franken (D-MN), Feinstein (D-CA), Blumenthal (D-CT), King (I-ME), Brown (D-OH), Kirk (R-IL), Schatz (D-HI), Schumer (D-NY), Murray (D-WA), Baldwin (D-WI), Booker (D-NJ), Hatch (R-UT), and Boxer (D-CA).

The text of the letter in its entirety can be found below:

Francis S. Collins, MD, PhD
Director, National Institutes of Health
Building 1, Room 126
1 Center Drive
Bethesda, Maryland 20814

Dear Dr. Collins:

We write to urge you to take steps to improve data collection on children participating in clinical trials funded by the National Institutes of Health (NIH). Investment in child health research is critical, not only to guarantee that children benefit from important scientific advances, but also to better understand how chronic diseases develop and persist later into adulthood.

As you know, NIH policy requires that children be included in NIH-sponsored clinical trials unless there is reason to exclude them. This is in line with policies already in place at NIH requiring the inclusion of women and minorities in NIH research. However, we are concerned that NIH is not systematically tracking the ages of children included in all of its clinical trials relevant to child health. For example, there is a big difference between a clinical trial that enrolls one seventeen-year-old, versus a clinical trial that includes tens, if not hundreds, of children of varying ages.

As a result, we are unable to determine whether children as a whole, or particular pediatric subpopulations, are underrepresented in federally funded biomedical research. This also leaves researchers with little information about how different pediatric subpopulations fare in these clinical trials. While NIH-funded research is required to include women and minorities to allow for the collection of data on the sex/gender and race/ethnicity of enrollees in clinical trials, the same principal has not been applied to children enrolled in clinical trials, even though this information is readily available.

Therefore, we ask that you improve data collection and report on the numbers of children in the various pediatric age groups enrolled in clinical studies. We are pleased with the ongoing work in Congress to address this issue and to improve representation in medical research more broadly. Too often, children get left behind as treatments are developed for adults, and we appreciate the work you have done to reverse this trend and improve access to treatments for children. It is critical that we continue to make progress on this front and ensure that the pediatric research community has access to this data to improve pediatric representation in clinical trials.

4/27/16