The study tested Apellis' pegcetacoplan in 80 paroxysmal nocturnal
hemoglobinuria (PNH) patients who remained anemic despite taking
Soliris. About half of them were even dependant on blood
transfusions to maintain optimal hemoglobin levels.
The trial results would help Apellis challenge Alexion's dominance
in the PNH market. Alexion's Soliris and Ultomiris, the only two
currently approved drugs for PNH, recorded sales of $1.08 billion in
the latest September quarter.
PNH is a rare, life-threatening disorder associated with abnormally
low hemoglobin levels due to the destruction of oxygen-carrying red
blood cells, making patients dependant on frequent blood
transfusions.
About 70% of PNH patients show low hemoglobin levels despite
treatment with Soliris and 36% require one or more transfusions a
year, according to Apellis. With pegcetacoplan, also called APL-2,
Apellis expects to address this unmet need.
Two-thirds of the Soliris-treated PNH patients cannot climb stairs
without pausing to catch their breath, Chief Executive Officer
Cedric Francois told Reuters.
"It all comes down to the quality of life... When these patients go
on APL-2, they can essentially have a life that is pretty much
normal."
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APL-2 will be rapidly adopted by patients who have seen an
inadequate response to Soliris and next-generation product Ultomiris,
Cowen analyst Phil Nadeau said ahead of the trial results.
Nadeau expects APL-2 to be launched in the United States in 2021
with penetration ramping to 28% in the PNH patient market in 2025,
driving $400 million in worldwide PNH sales.
Th drug, which targets an immune pathway known as the complement
system, is also being tested in other indications such as geographic
atrophy and complement-associated kidney diseases.
Pegcetacoplan was as effective as Soliris in reducing patient
dependence on blood transfusions, a secondary goal of the study,
Apellis said.
(Reporting by Trisha Roy and Manojna Maddipatla in Bengaluru;
Editing by Shinjini Ganguli)
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