CHICAGO/TOKYO (Reuters) - Shares of Eisai Co Ltd plunged as much as 21 percent after the results of its experimental Alzheimer’s drug being developed with partner Biogen Inc failed to enthuse investors.
In a highly anticipated mid-stage trial, patients in the early stages of the disease treated with the drug, BAN2401, experienced 30 percent less cognitive decline than those who got a placebo.
The second-highest dose of the drug also showed some benefit, but did not meet statistical significance, according to data presented on Wednesday at the Alzheimer’s Association International Conference in Chicago.
Investors, who had bid up Biogen and Eisai shares earlier this month after the companies said the drug was effective at the highest dose, sold off shares after the presentation of the details.
Eisai shares fell as much as 21 pct before ending 10 percent lower in Tokyo trading. The shares touched a record high on Wednesday ahead of the Chicago presentation. Biogen shares fell more than 11 percent in extended trading to $340.
The fall came despite Alzheimer’s experts welcoming the results.
“Overall, it’s a shot in the arm for the field,” said Dr. Ronald Petersen, from the Mayo Clinic in Rochester, Minnesota.
“It rejuvenates some of the enthusiasm for attacking amyloid, that it is possible and may be successful,” he said of the theory that removing toxic deposits of the protein beta amyloid from the brain will disrupt Alzheimer’s progression.
BAN2401 demonstrated a dose-dependent reduction in amyloid plaques that was statistically significant at all doses tested, researchers said.
However, analysts pointed to concerns including that at lower doses of the drug outcomes were poorer than placebo.
“I think the dose response is very clear,” Masanori Tsuno, Deputy Chief Clinical Officer at Eisai’s Neurology unit, said of that concern at a briefing in Tokyo.
“In order to show the clinical efficacy we need to reach a certain degree of amyloid beta clearance... until you reach that threshold you will not see the clinical signs,” he said.
There is a desperate need for an Alzheimer’s treatment that works after dozens of failures of experimental drugs. The most common form of dementia affects nearly 50 million people worldwide and is expected to rise to more than 131 million by 2050, according to Alzheimer’s Disease International.
The BAN2401 trial involved 856 patients with early Alzheimer’s disease who had beta amyloid in their brains as confirmed by brain scans. The highest does of 10 mg/kg bi-weekly - one of five doses tested - was given to 161 patients.
A key concern was that for safety reasons a regulator outside the United States stipulated that carriers of a gene mutation called APOE4 associated with earlier onset of Alzheimer’s not receive the highest dose of the drug. These people had been more prone to a brain swelling side effect in earlier trials known as amyloid-related imaging abnormalities-edema, or ARIA-E.
That resulted in 26 people being moved out of the highest dose cohort. Analysts on a Biogen conference call asked if that imbalance might confound the results. Dr. Alfred Sandrock, Biogen’s chief medical officer, said a subgroup analysis was underway to look at the issue.
Baird analyst Brian Skorney said the difference resulted in a “huge imbalance.”
“We expect a sell-off tomorrow as the irrational exuberance burns off, but would be looking for an opportunity to be buyers if it goes too far,” he said of Biogen stock.
The companies have said they are planning large late-stage trials in which they must replicate positive results. Eisai’s Tsuno said they would like to discuss getting conditional approval for the treatment with U.S. regulators.
STILL A LOT OF QUESTIONS
The results, based on traditional statistical methods after 18 months of treatment, followed 12-month results that failed to meet the study’s main cognitive decline goal based on a complex predictive Bayesian statistical model.
Dr. Julie Schneider, an Alzheimer’s expert with Rush University Medical Center, said more work is needed to understand how much of a clinical effect the drug has.
“We don’t know how many went on to get Alzheimer’s dementia. I think there’s still a lot of questions,” she said.
Alzheimer’s experts at the briefing for journalists expressed concern about the measurement devised by Eisai - a compilation of conventional cognitive assessment tools called ADCOMS. The Japanese drugmaker felt a new measurement approach was needed to capture early cognitive changes in patients at the beginning stages of Alzheimer’s decline.
They also raised concerns that while the drug slowed cognitive decline, such as memory loss, the disease was not arrested and patients continued to experience decline over the 18-month treatment period.
Nevertheless, using a more conventional measure of cognition known as ADAS-cog, the highest dose of the treatment led to a statistically significant 47 percent reduction in cognitive decline at 18 months compared with patients taking a placebo.
“I’m impressed,” Dr. Howard Fillit, chief science officer of the Alzheimer’s Drug Discovery Foundation, said of the results.
Fillit said a 30 percent reduction using the more traditional ADAS-cog scale, which is a hard target to budge, is considered clinically meaningful.
“This result might be clinically meaningful if it’s reproduced,” he said. “I’m a skeptic, but I think there’s something here.”
Reporting by Julie Steenhuysen in CHICAGO and Sam Nussey in TOKYO; Additional reporting by Junko Fujita; Editing by Bill Berkrot and Sunil Nair
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