GAIN AND LOSS IN MALARIA WAR - C&EN Global Enterprise (ACS

Mar 10, 2008 - The Institute for OneWorld Health has signed on Sanofi-Aventis and Amyris Biotechnologies to develop a low-cost semisynthetic route to ...
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NEWS OF THE W EEK

PIPELINE: Ambitious ventures

launch as GSK pulls two treatments for the disease

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HE FRUSTRATING BATTLE against malaria took two steps forward and one step back last week. New ventures targeting more affordable and effective treatments were launched, but they came on the heels of a setback in the antimalaria drug pipeline. The Institute for OneWorld Health has signed on Sanofi-Aventis and Amyris Biotechnologies to develop a low-cost semisynthetic route to artemisinin, the active pharmaceutical ingredient (API) in a range of malaria drugs. The API is currently extracted from the sweet wormwood plant, and the companies say a nonseasonal source would help stabilize the supply and price of malaria treatments. The goal is to design a commercial-scale manufacturing process that will turn out enough API to treat 200 million people—about 40% of the population that contracts malaria each year. The project builds on technology developed by University of California, Berkeley, professor Jay Keasling, who developed a microbial system to produce artemisinin through fermentation. “This collaboration enables us to reach a goal that some scientists only dream of,” says Jack Newman, senior vice president of Amyris. “What started as a breakthrough in the lab can now evolve into a real solution that will truly make a difference in the world.” The partnership taps into Amyris’ experience in engineering microbial strains and Sanofi-Aventis’ expertise in fermentation and chemistry process devel-

opment. The companies aim to incorporate their semisynthetic product into artemisinin-based combination therapies by 2010. While some scientists are working to ensure a more steady supply of existing medicines, others are developing new treatments. Last week, the PATH Malaria Vaccine Initiative and Seattle Biomedical Research Institute (SBRI) announced plans to establish the Human Challenge Center (HCC), a facility in Seattle dedicated to testing new malaria vaccines in human volunteers. The plan for the center is to evaluate vaccine candidates that disrupt the malaria parasite along different points in its development. HCC is the next component of the Malaria Clinical Trials Center, a facility at SBRI intended to bring together basic science and clinical research. A vaccine would add a muchneeded weapon in an ever-depleting arsenal against malaria. On top of the resistance that has rendered some drugs ineffective, safety concerns have recently diminished the antimalarial pipeline. GlaxoSmithKline announced late last month that it is recalling Lapdap, a combination of chlorproguanil and dapsone, and discontinuing development of Dacart, a therapy that combines chlorproguanil, dapsone, and an artemisinin derivative. According to GSK, results from a Phase III trial comparing Dacart with Novartis’ Coartem, which also contains an artemisinin derivative, indicated that trial participants with an enzyme deficiency had significantly lower levels of hemoglobin in their blood, a condition that can cause anemia. In a separate trial, Lapdap, which was sold only in Kenya, was also shown to lower hemoglobin in that patient group.—LISA JARVIS STEVE R ING M A N/S EATTLE TIMES /M CT/NEWSCOM

GAIN AND LOSS IN MALARIA WAR

A baby receives a malaria vaccine in a trial in Tanzania.

CHINA PETROCHEMICALS Coastal projects face opposition from local residents Two large petrochemical projects planned for construction in affluent parts of China are facing tough opposition on environmental grounds from local residents. Last week, demonstrations that occasionally turned violent were held on the island of Dongshan, in Fujian province. International newswires and the Hong Kongbased South China Morning Post reported that thousands of people participated. Dongshan residents, many of whom earn a living from fishing, oppose the construction of a $1.4 billion p-xylene plant by Taiwan-funded Tenglong Aromatic. It would be located on Gulei, a peninsula that reaches out from the mainland to

within 2 miles of the island. Tenglong originally intended to build the plant in Xiamen, 75 miles north of Dongshan, but the project ran into spirited opposition from that city’s well-to-do middle class (C&EN, June 11, 2007, page 17). Meanwhile, in the southern province of Guangdong, China’s state media report, 14 provincial legislators are moving to postpone the construction of an $8 billion refinery and petrochemical complex promoted by China Petroleum & Chemical Corp. (Sinopec) and its partner, Kuwait Petroleum. The project was reportedly approved last November by China’s National Development & Reform

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Commission, but the legislators say a full environmental impact review has not been conducted yet. Jia Yiqun, a Sinopec spokesman in Hong Kong, tells C&EN that it’s too early to get excited. “We’re still only in talks with the Kuwaiti government,” he says, noting that the project was initiated by Kuwait. “We have not completed the feasibility study yet.” Residents of Nansha, an industrial suburb of Guangzhou, where the project is supposed to be built, have in the past expressed concerns about pollution from the chemical industry (C&EN, Jan. 8, 2007, page 32).—JEAN-FRANÇOIS TREMBLAY