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Intrexon Corporation (NYSE: XON), a leader in synthetic biology, announced today that it has entered into a research and development collaboration with Johnson & Johnson Innovation and its affiliate Johnson & Johnson Consumer & Personal Products Worldwide, a division of Johnson & Johnson Consumer Companies, Inc., to advance new skin and hair care products.

“We look forward to advancing new skin and hair beauty products that have measurable impact for consumers,” said Randal J. Kirk, Chairman and Chief Executive Officer, Intrexon.  “By combining Intrexon’s synthetic biology approaches with the capabilities at Johnson & Johnson Innovation and Johnson & Johnson Consumer & Personal Products Worldwide, we believe that there are multiple areas for new product exploration.”

Neuralstem, Inc. (NYSE MKT: CUR) announced today that it has entered into agreements with leading institutional investors for a registered direct placement (the “Offering”) of 6,752,744 shares of common stock at a price of $2.91 per share, resulting in aggregate gross proceeds of approximately $19.65 million.

In addition, the Company will issue to each investor a warrant to purchase a number of shares of common stock equal to one-half of the number of shares purchased by the investor in the Offering. The warrants have an exercise price of $3.64 per share, and are exercisable from the issuance date, for a period of five years.

Elliott Sigal has opened the next chapter of his career. The former R&D chief at Bristol-Myers Squibb ($BMY), who helped squire a number of blockbuster programs through the clinic, is joining David Mott as a venture partner at New Enterprise Associates.

Bristol-Myers’ R&D group had its setbacks, particularly in 2012, but during Sigal’s tenure at the top of the research arm he guided an amazing 14 drugs to an approval, including Abilify, Erbitux and Onglyza. Those were all part of Bristol-Myers’ “string of pearls,” which earned the company a rep as one of the leaders in innovation in the field. Few other R&D chiefs–including a number who had much larger budgets to work with–even came close.

GlaxoSmithKline plc [LSE/NYSE: GSK ] announced today that the U.S. Food and Drug Administration (FDA) has approved Mekinist® (trametinib) for use in combination with Tafinlar® (dabrafenib) for the treatment of patients with unresectable melanoma (melanoma that cannot be removed by surgery) or metastatic melanoma (melanoma which has spread to other parts of the body) with BRAF V600E or V600K mutations. These mutations must be detected by an FDA-approved test.1 Tafinlar is not indicated for treatment of patients with wild-type BRAF melanoma.2

The approval of the combination is based on the demonstration of response rate and median duration of response in a Phase I/II study. Improvement in disease-related symptoms or overall survival has not been demonstrated for Mekinist in combination with Tafinlar.1 The combination was approved through the FDA’s Accelerated Approval programme and reviewed under a Priority Review designation.3 This accelerated approval is contingent on the results of the ongoing Phase III trial (referred to as MEK115306 or Combi-D), which is designed to evaluate the clinical benefit of the combination in this patient population.

The International CES expo in Las Vegas, which kicks off Tuesday, has long been the site of new technology announcements and gadget demonstrations. This year, about 55 Washington area companies plan to exhibit at the show, up slightly from last year’s 53.

The group represents one of the most diverse that the region has sent to Las Vegas, said Jeff Joseph, senior vice president for communications with the Consumer Electronics Association, which puts on the show.

The healthcare industry will continue to command the spotlight in 2014, and healthcare executive search consultants from Witt/Kieffer have some advice for making 2014 a stellar year on the work front, including a recommendation to broaden the role of the CIO.

The recommendations:

Prepare for unplanned CEO turnover – Paul Bohne, managing partner, says, “Technological advancements, physician alignment, market consolidation and government policy changes have all increased the complexities of how large, diverse healthcare organizations operate.” These mounting responsibilities have exacerbated the turnover issue.

New survey data result in an upward revision of the previously published 2011 U.S. research and development performance total and imply a sizable further expansion in 2012. These new data puts U.S. R&D expenditures at $428.2 billion in 2011,[2] an increase of $20.5 billion over the 2010 level ( table 1, figure 1 ). The preliminary estimate of the 2012 U.S. total for R&D is $452.6 billion.

As we go into the last few weeks of the year, my office is busy working up the final numbers on application data for this year. Although the complete set of application data, tables, and graphs will not be available until later in January, I thought I would provide an early snapshot on success rates for 2013 competing research project grant (RPG) applications and awards.

We received 49,581 competing RPG applications at NIH in fiscal year 2013, slightly declining compared to last year (51,313 applications in FY2012).

A 15-minute commute from Baltimore to Washington, D.C., might be a possibility after all.

The Greater Baltimore Committee in 2012 supported a plan to use maglev trains to produce the next generation of high-speed rail in the Northeast corridor.

But the love affair eventually faded and talk of maglev trains coming to the Baltimore area waned. But the Japanese government is promising to lend the United States half the cost of building the first “Super-Maglev” train. The high-speed train would reduce the 37-mile commute between Baltimore and D.C. from one hour to a blazing-fast 15 minutes

The Tech Council of Maryland (TCM), Maryland’s largest technology trade association, released its 2014 Policy Platform, which outlines the organization’s specific priorities in the areas of advanced technology, life sciences, taxation, transportation, higher education and workforce development. TCM’s advocacy efforts during the 2014 session of the Maryland General Assembly, which begins January 8, will focus on further improving the business climate to encourage technology and biotechnology companies to grow and flourish in the state.

Specifically, TCM’s 2014 Policy Platform urges policymakers to increase funding for innovation incentives, such as the Research and Development Tax Credit, the Biotech Tax Credit and the Stem Cell Research Fund, and reject onerous changes to the tax structure, such as combined reporting, to provide more certainty for the technology and life sciences business communities. In addition, TCM would like to see implementation of continued long-term funding and policy solutions for development of Maryland’s transportation infrastructure, higher education institutions and next-generation workforce.