Orphan drug sales reach $242bn by 2024, according to EvaluatePharma®
Orphan Drug Report 2019
LONDON & BOSTON & TOKYO–(BUSINESS WIRE)–lt;a href="https://twitter.com/hashtag/biopharma?src=hash" target="_blank"gt;#biopharmalt;/agt;–Scientific advancements will help propel the orphan drug market to a 12%
CAGR to 2024, double the 6% rate expected for non-orphan products. In
addition to recent breakthrough cell and gene therapy products like
Yescarta and Luxturna, a number of “one and done” treatments for orphan
diseases are approaching the market, including Novartis’s Zolgensma and
bluebird bio’s Lentiglobin.
The explosion of new technologies brings their high price points into
greater focus — for example, the $425,000 per eye list price for Spark’s
Luxturna is the value-based price agreed on with Spark and payers. In
2018, the mean cost for an orphan drug was 4.5 times that of a
non-orphan product.
Despite the clear advancements in treatment, however, those calling for
reform of the Orphan Drug Act may gain further ammunition. Big pharma
continues to entrench their position in the orphan market, as evidenced
by Bristol-Myers Squibb’s bid for Celgene, Roche’s pending acquisition
of Spark, and Novartis’s $8.7bn payment for Zolgensma.
“Seven of the top 20 R&D orphan products by net present value are either
a cell or a gene therapy,” said report author Karen Pomeranz, PhD.
“However, we may not see the full market impact of these drugs by 2024,
which means that the long-term growth and patient benefits could be even
more pronounced.”
Additional report highlights include:
-
The mean cost per patient per year of the top 100 orphan products was
$150,854 in 2018, compared to $33,654 for a non-orphan drugs. -
Blood, CNS and respiratory are the leading orphan drug therapeutic
areas, accounting for more than 50% of the non-oncology orphan drug
market. -
In 2024, Celgene, Abbvie and Johnson & Johnson will lead the oncology
orphan drug market, accounting for approximately 30% of worldwide
sales. -
Vertex’s triple combination for cystic fibrosis is the most valuable
R&D orphan product, with an estimated NPV of $24bn. -
The orphan drug pipeline is anticipated to contribute $187.7bn in
sales by 2024, 35% of the combined forecast for all pipeline products.
Download your complimentary copy of the “EvaluatePharma® Orphan
Drug Report 2019” at http://www.evaluate.com/OrphanDrug2019.
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