In that sense, Quark is still a chameleon, by which I don’t mean anything pejorative — biotechs turn on a dime all the time, often for very good reasons (failed clinical trials, for instance, being a prime example). Some biotechs, however, reinvent themselves for less admirable ends, such as shifting gears to catch rising investor enthusiasm for a sexy new technology or drug-development strategy. In that earlier post, I raised the possibility that Quark had done exactly that by licensing its experimental RNAi drugs from another company and then rushing to declare itself a pioneer in RNAi therapy.
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After looking into the Silence-Quark partnership more deeply, my current understanding is that Quark developed both its leading RNAi candidates with help from Silence, but only licensed certain nucleic-acid chemistry from its partner, not the RNAi molecules (or sequences) themselves. The bottom line is that Quark appears much more justified in its claim to be a leader in RNAi therapeutic development than I originally thought.
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Before getting into all that, a quick update on Quark’s recent funding efforts. Gavin Samuels, the company’s VP for business development and investor relations, says Quark has lined up a syndicate of investors who have pledged roughly $20 million of the company’s intended $30 million funding round. The final $10 million may be provided by new investors who join that syndicate, although Samuels said Quark may also simply wait another three months or so to raise those funds. One factor weighing on the company is a pending “milestone” payment Quark is expecting soon from Pfizer, and whether that will be enough to carry the company into mid-2009 without the need to raise another $10 million. (Biotechs love such milestone payments, which are typically “non-dilutive” cash infusions that don’t shrink startup founders’ ownership stakes or require other existing investors to pony up in order to maintain their stake in a company.)
Samuels also told me that Quark’s abortive IPO last year foundered for both internal and external reasons, including market jitters following the huge Blackstone Group IPO last June that hit right as Quark was hoping to price its offering. The company itself, however, wasn’t blameless, he says. For instance, Quark may have jumped the gun by trying to go public when it only had one drug in early-stage human testing; in addition, Samuels says, the startup hadn’t done enough to make its case with journalists and market analysts.
Anyway, on to the convoluted history of Quark and Silence after the jump.
Most of the confusion involves Quark’s two leading RNAi therapeutic candidates, each known by an alphabet-soup moniker: RTP801i-14, which targets a gene called RTP801 and is now in human tests as a treatment for age-related macular degeneration, and AKIi-5, which inhibits an apoptosis (programmed cell death) gene called p53 and which Quark is now testing against acute kidney injury. In April 2005, Quark struck a partnership (referenced here) with Silence — then known as SR Pharma — in which it received the right to use a Silence chemical-modification technology called AtuRNAi to stabilize RNAi molecules for use as drugs. The two companies also filed a joint patent application on the structure and sequence of RTP801i (the fundamental IP on AKIi-5, by contrast, is wholly owned by Quark). Quark subsequently licensed RTP801i-14 and some related compounds to Pfizer, which is now running clinical trials.
Silence, however, subsequently chose to characterize the partnership in a manner that suggested Quark had simply acquired its drug candidates directly from Silence. For instance, this July 27, 2007 press release notes that Silence “has sublicensed the AtuRNAi compound RTP-801i to Pfizer through its collaboration partner Quark Biotech,” and that “Silence Therapeutics has licensed a further AtuRNAi compound, AKIi-5, to Quark Biotech.”
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“We had a not-insignificant problem with the way that was characterized,” Quark’s Samuels told me. “It sounds like they have this compound and hired two contractors, Quark and Pfizer, to develop it. That’s not the case.” (Samuels should know: He previously worked for Pfizer and, while there, negotiated the company’s deal for RTP801i-14 with Zurr.)
Jeffery Vick, who became CEO of Silence last July, told me that “it’s difficult in press releases to capture the whole relationship” between his company and Quark, which is about as close as he got to acknowledging the fundamentally misleading phrasing Silence had used. Silence, however, quickly altered its wording in recent press releases to refer more specifically — and accurately — to the two experiimental drugs. On July 30, 2007 — just three days after Vick was appointed CEO –Silence noted in this release (PDF link) that its AtuRNAi technology “has also been sublicensed to Pfizer by Quark Pharmaceuticals, through Quark’s license of the compound RTP-801i-14,” and further states that Quark “has developed a further compound, AKIi-5, having AtuRNAi structure under the existing licence from Silence Therapeutics.”
So that’s the story, for the half-dozen or so of you who care enough to have read this far. As I said, the actual facts behind the collaboration, which I confirmed with both companies, do support Quark’s claim to be more of an RNAi leader than the follower it initially appeared to be, although it’s equally clear that it didn’t get there by itself. Chalk this one up to some overzealous PR on the part of Silence, which fortunately appears to have seen the light since then.
CORRECTED: Updated with some minor corrections about the provenance and target of AKIi-5.
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