Global Times - Weekend

Japan’s Astellas buys Audentes

Gene therapies aim to cure diseases by replacing missing, mutated versions of genes with healthy copies

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Japan’s Astellas Pharma Inc is buying US drugmaker Audentes Therapeuti­cs Inc for about $3 billion in cash, in a high-priced push to make genetic medicines a key area of growth.

Gene therapies are one of the hottest areas of drug research and Astellas, Japan’s second-largest drugmaker by sales, is offering $60 per share for San Francisco-based Audentes.

Citi analyst Hidemaru Yamaguchi said that while the deal looked expensive, it was a positive move for Astellas as Audentes had “cuttingedg­e gene therapy modalities”.

“We thought it was only a matter of time before Astellas entered the gene therapy market,” he wrote in a note for clients, adding it had already licensed developmen­t rights for a domestic gene therapy in Amyotrophi­c lateral sclerosis.

Gene therapies aim to cure diseases by replacing the missing or mutated version of a gene found in a patient’s cells with healthy copies. With the potential to cure devastatin­g illnesses in a single dose, drugmakers say they justify prices well above $1 million per patient.

“As a result of this acquisitio­n, Astellas will obtain not only Audentes programs but also its proprietar­y manufactur­ing knowhow in gene therapy,” Astellas CFO Naoki Okamura told a briefing in Tokyo. “Internal manufactur­ing capability is a great strength for companies with multiple programs under developmen­t.”

Genetic drugs will become a fifth primary focus for Astellas, Okamura said, joining existing business lines in regenerati­ve, immuno-oncology, immunother­apy and neuro-muscular medicine.

The acquisitio­n marks the secondbigg­est on record for Astellas after its 2010 purchase of OSI Pharmaceut­icals Inc for$3.8 billion, according to Refinitiv data. Astellas expects the deal, which is subject to regulatory approval including US antitrust clearance, to close in the first quarter of 2020.

Audentes’ investigat­ional drug, AT132, is being developed to treat a rare genetic neuromuscu­lar disorder that results in extreme muscle weakness, respirator­y failure and in some cases early death.

Astellas said the companies plan to seek FDA approval for AT312 in mid-2020.

The drug has shown promising results in the treatment of X-linked myotubular myopathy, seen mainly in male infants, it said.

Only about 40 boys are born in the US with the condition each year, so that would yield just $80 million in revenue, said Jefferies analyst Stephen Barker, assuming a maximum price tag for the treatment.

“The $3 billion acquisitio­n price is therefore more likely to be mainly predicated on the firm’s technology platform and manufactur­ing capabiliti­es,” Barker wrote in a note.

The deal also marks the latest consolidat­ion in the industry, which saw Japan’s Takeda Pharmaceut­ical Co acquire Britain’s Shire for $59 billion.

 ?? Photo: VCG ?? A technician handles samples at a Prenetics Inc laboratory in Hong Kong, China in January 2018.
Photo: VCG A technician handles samples at a Prenetics Inc laboratory in Hong Kong, China in January 2018.

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