Alnylam Looks to ASCO as First “Bell-Ringing” for RNAi Resurgence

5/26/11Follow @arleneweintraub

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a trial of ALN-PCS, which is designed for patients with severely high cholesterol who don’t respond to traditional statins. “We think these are going to be pretty important for the whole RNAi field,” Maraganore says.

The first hurdle, though, is the ASCO conference. ALN-VSP02 targets two genes that promote the growth and development of cancer cells: vascular endothelial growth factor (VEGF) and kinesin spindle protein (KSP). This drug is important for Alnylam not just because of its potential value against liver cancer, but also because it is the company’s first RNAi treatment designed to circulate throughout the bloodstream—the way it hopes to deliver other experimental treatments in the future. The abstract for the trial of ALN-VSP02, which was published May 18, says the drug is well tolerated and is showing activity “consistent with an anti-VEGF effect” that it is shooting for. Maraganore says further details on the trial—and the patient who has been on the drug for 12 months—will be provided at the meeting.

He hopes pharmaceutical executives will be paying attention, because Alnylam is looking to ally with another company to take the drug into Phase 2 clinical trials. “ASCO will be important for that program’s partnership potential,” he says. “For Alnylam it’s also important, because in a sense, it’s a bell-ringing for this drug class.”

Maraganore points out that there are still plenty of drugmakers interested in RNAi. Alnylam has ongoing partnerships with such pharma giants as Takeda Pharmaceuticals, GlaxoSmithKline (NYSE: GSK), and Cubist Pharmaceuticals (NASDAQ: CBST). And Merck (NYSE: MRK), which was an early investor in the technology, is still researching RNAi therapeutics. “Other companies remain committed to this field,” he says.

As for the drop of Alnylam’s stock, Maraganore isn’t worried. “Obviously it caused anxiety, but for Alnylam it hasn’t changed a thing,” he says. The company has $343 million in cash on its books, placing it in the top 12 in the biotech industry in net cash positions, according to Alnylam’s internal analysis. It helped that when Roche came aboard in 2007, Alnylam got $331 million right off the bat. “That was an enormous amount of money up front,” Maraganore says.

Maraganore can’t comment on the Tekmira suit because of the ongoing dispute. At the time, he told Xconomy that the suit was a “big surprise” and the allegations were “completely untrue.” The dispute hasn’t disrupted the manufacturing partnership the two companies have on ALN-VSP02, he says.

The ASCO conference will also feature a presentation by Silence Therapeutics, a UK-based company that’s developing an RNAi drug to treat solid tumors. Maraganore hopes that data will help build positive attention for the beaten-down technology. “These are evolutionary trials,” he says. “But we’re pretty excited. As these bells get jingled, increasingly it will be a resounding sound.”

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  • Homer Yeh

    I believe it is worth to give RNAi a trial from molecular point of view since cancer is a molecular disease. From theorectical point of view, using RNAi for gene silencing is nothing wrong but a perfect approach. But unlike monoclonal antibodies that tackles antigenic epitodes that are located on the surfaces of the cells. Those mutated genes are usually located deep in the nuclear of malignant cells, having problems of accessibility. But that is not a problem that can’t be overcome. It may take a little while to find ways of problem solving. In math, key to the problem solving usually is located in the problem itself. Good luck! Ms. Maraganore!

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