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Sanofi pays $50 million for Revolution Medicines’ SHP2 inhibitor

The partners expect to begin clinical studies of the compound later this year

by Lisa Jarvis
July 18, 2018 | APPEARED IN VOLUME 96, ISSUE 30

Credit: Revolution Medicines
Revolution Medicines' CEO Mark Goldsmith.

In its first major deal, Revolution Medicines will receive $50 million from Sanofi in exchange for sharing rights to its lead drug candidate, the SHP2 inhibitor RMC-4630. The Redwood City, Calif.-based firm could see another $500 million in milestone payments as the allosteric inhibitor winds towards the market.

When Sanofi and Revolution begin clinical trials of RMC-4630 in the second half of the year, it will be the first time one of the biotech’s compounds is tested in humans.

Revolution was launched in 2015 based on technology developed in the labs of University of Illinois, Urbana-Champaign, organic chemist Martin D. Burke, who a year earlier had unveiled a method for easily creating complex molecules—in some cases natural products never before synthesized—from a dozen basic building blocks.

Burke’s group then invented a machine that uses plug-in cartridges containing those building blocks to automate compound assembly. Revolution subsequently worked to turn Burke’s lab prototype into a commercially robust machine. The company has also broadened its drug discovery capabilities while narrowing its therapeutic focus to cancer.

Revolution identified SHP2 as an intriguing oncology target within its first year of operation. Because the biology around the enzyme was not well known, the firm’s scientists first had to develop tool compounds to probe it.

In collaboration with University of California, San Francisco, medical oncologist Trever Bivona, the researchers figured out that when certain players in the cancer-connected Ras/MAP kinase signaling pathway are mutated, they become dependent on SHP2 to amplify their signal. Revolution developed RMC-4630 to inhibit SHP2.

Sanofi and Revolution can now test its drug in people with cancers featuring such mutations, which Revolution CEO Mark A. Goldsmith says account for up to 20% of non-small-cell lung cancer cases, for its clinical studies of RMC-4630. “For those tumors, there are no precision oncology or targeted therapeutics available today,” he adds.

The partnership with Sanofi gives Revolution the financial freedom to develop other compounds in its pipeline on its own. Although Revolution isn’t averse to other collaborations, “with this deal in place, I think we have no pressure to do any other deals around our other programs,” Goldsmith says.”



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