Report reveals gap between rare-disease drug spending, need

By Jenni Spinner contact

- Last updated on GMT

(EugeneOnline/iStock via Getty Images Plus)
(EugeneOnline/iStock via Getty Images Plus)

Related tags: Rare disease, orphan disease, Drug development, Research and development, IQVIA

The IQVIA and NORD study shows rare-disease treatments account for only 11% of new drug spending, but 80% of orphan products treat rare diseases alone.

A new report released by IQVIA and commissioned by the National Organization for Rare Disorders (NORD) found that while 79% of orphan products treat only rare diseases, orphan conditions account for only 11% of drug spending in the US. The study also shows recent progress in drug development has led to more rare-disease patients having access to much-needed treatments.

As of January 1, 2020, 564 orphan products were approved by the US Food and Drug Administration (FDA) to treat 838 rare diseases, or "indications". About 30% of all orphan indications were approved in the three years prior to the study, based on 2019 data.

According to the report, multiple uses for the same medicine have become increasingly common, particularly with regard to cancer and autoimmune diseases, as improved understanding of biological pathways allows for a single therapy to treat numerous rare and common conditions. Interestingly, most orphan products still are used to treat only one rare disease.

The study also demonstrates that patients are gaining access to multiple treatment options, thanks to generics and biosimilars entering the market. This occurs in many cases even when there is a term of orphan drug exclusivity in effect.

Peter Saltonstall, president and CEO of the National Organization for Rare Disorders (NORD), said drug pricing is an important issue that affects everyone in the US and needs to be addressed.

“Our hope is for this data to raise awareness of the critical need for new rare disease treatments, and demonstrate that the overall amount spent on those treatments is small compared to the total drug spend in the US​,” he said. “People with rare diseases need help, and the Orphan Drug Act is important for spurring innovation​."

Since 2010, the share of orphan drug spending has increased by five percentage points, likely due to the increasing number of approved orphan products. Over this same time period, specialty drug spending also has increased by 22 percentage points, now accounting for 47% of all medical invoice spending.

However, specialty drugs and orphan drugs are not the same. The IQVIA report found 77% of specialty drug spending goes toward the treatment of common conditions, not toward rare diseases.

Approximately 7,000 known rare diseases affect more than 25m Americans. Rare diseases tend to be chronic, serious and life-threatening. Approximately 80% of rare diseases are genetic in origin. More than 90% of rare diseases have no treatment.

The report "Orphan Drugs in the United States: Rare Disease Innovation and Cost Trends Through 2019," is available at NORD commissions the study every two years to examine the state of drug development for rare diseases as part of its mission to support people with rare diseases.

(EugeneOnline/iStock via Getty Images Plus)

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