By Puyaan Singh
April 13 (Reuters) – IDEAYA Biosciences and French pharma company Servier said on Monday their combination drug for a type of eye cancer met the main goal of a mid-to-late-stage trial, sending the U.S. biotech’s shares 21% higher.
IDEAYA will now apply for the U.S. Food and Drug Administration’s approval in the second half of the year, seeking to enter a market with no approved treatments in the country.
The drug, darovasertib, in combination with Pfizer’s Xalkori, improved survival without progression of uveal melanoma by a median of 6.9 months, compared with 3.1 months for other chosen therapies.
The investigator-chosen therapies were either Merck’s Keytruda or a combination of Bristol Myers Squibb’s Opdivo and Yervoy, commonly used off-label to treat the disease.
In the 313-patient study, there were five complete responses, or disappearance of all detectable signs of cancer, in the darovasertib combination arm, compared with zero in the other arm.
Guggenheim analyst Paul Jeng said conversations with a physician suggest adoption of darovasertib will be “rapid and robust.”
Uveal melanoma is a rare, aggressive form of eye cancer that usually spreads to other parts of the body, mainly the liver. Around 10,000 new cases are reported globally every year.
Around 20% of patients require enucleation, for which the eye is removed, while others may need radiation treatments that may cause permanent vision loss, Darrin Beaupre, IDEAYA’s medical chief, said.
The company has been able to “save 60% of eyes for patients who would otherwise require enucleation,” he said.
Between 50% and 70% of people whose cancer has spread to other parts are of the HLA-A*02:01-negative serotype targeted by the drug, the companies said.
Immunocore’s Kimmtrak is the only therapy approved for the HLA-A*02:01-positive serotype, for which darovasertib is also being tested.
Truist’s Gregory Renza expects peak annual revenue of around $1.7 billion for darovasertib.
(Reporting by Puyaan Singh in Bengaluru; Editing by Sahal Muhammed)

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