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Obama's Proposal To Redirect Abstinence-Only Funding Renews 'Culture-War Battle,' Washington Times Columnist States
President Obama is causing the "core culture-war battle" over sex education to "come full circle" by proposing to redirect funding for abstinence-only sex education to a new Teen Pregnancy Prevention Initiative that "rejects an abstinence-only approach," Washington Times columnist Cheryl Wetzstein writes. According to Wetzstein, Obama"s fiscal year 2010 budget plan "zeroed out" the Title V abstinence-only sex education grant program, set to expire on June 30, and the Community-Based Abstinence Education program. Wetzstein continues that groups supporting comprehensive sex education have "loathed Title V from its inception" because of its "prohibition on teaching teens how to use birth-control products (i.e., no condom demonstrations) and its eight-point definition that seemed utterly unrealistic to sex educators." For example, Title V"s definition said that the ""expected standard of human sexual activity"" was a ""mutually faithful, monogamous relationship in the context of marriage,"" which Wetzstein says she has "heard many times, was insulting to gay youth who couldn"t marry" and "insensitive to minority youth who grew up in neighborhoods where marriage was rare." Wetzstein asks, "What will happen to Title V?" She writes that opponents "are staying vigilant" and working to avoid "any last-minute, back-door revivals of this program." Groups that support abstinence-only sex education are "working the phones, too," Wetzstein reports. According to Wetzstein, Valerie Huber, executive director of the National Abstinence Education Association, noted that "[s]aving Title V will require some heavy lifting, but "it"s expired before and been retroactively renewed."" Wetzstein concludes that "we"ll soon see what happens with the new players in town" (Wetzstein, Washington Times, 6/23).
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Tobira Therapeutics Inc. Announces Phase I Data Demonstrating Pharmacokinetic Properties Of TAK-652 For The Treatment Of HIV
Tobira Therapeutics Inc., a clinical stage biotechnology company committed to research and product discovery for the treatment of life-threatening and life-altering infectious diseases, today announced pharmacokinetic data and results from two Phase I pharmacokinetic studies for TAK-652, an investigational compound being developed for the treatment of HIV. These data suggest that TAK-652 is rapidly absorbed and demonstrate relatively good oral bioavailability (as shown by the plasma TBR-652 concentration data) and has a long plasma half-life of TBR-652 (approximate mean of 35 hours) supporting once-daily dosing. Mean TBR-652 plasma concentrations were well above the predicted target plasma concentration (2ng/mL) with or without food. In both studies TBR-652 was safe and well tolerated in this healthy subject population when administered over a dose range of 10 mg to 800 mg in 2 tablet formulations. "These two Phase I studies provide encouraging support for TAK-652 as a therapeutic option for the treatment of HIV. We look forward to results from our on-going proof-of-concept study," said James Sapirstein, CEO.
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Roswell Park Awarded $2.8 Million Grant To Study Ovarian Cancer
The National Cancer Institute has awarded a five-year, $2.8 million Research Project (RO1) grant to Roswell Park Cancer Institute http://www.roswellpark.org/ (RPCI) researchers to investigate the role of immunological pathways in the development of ovarian cancer.
Cardiovascular

Congress Introduces Bill To Ensure Continuous Domestic Supplies Of Common Medical Isotope

SNM and a coalition of eight other organizations have issued a white paper urging Congress to take steps to maintain adequate supplies of Molybdenum-99 (Mo-99), a radioactive substance that is the basis for a common medical isotope used in more than 80 percent of all nuclear medicine procedures. The coalition jointly issued the paper to ensure that patient care is not compromised by a worldwide shortage of Mo-99 and measures to curtail the use of high-enriched uranium (HEU) in radionuclide production as a non-proliferation strategy. In response, U.S. Representative Edward Markey (D-Mass.) introduced legislation (H.R. 3276) reflecting many of the coalition"s concerns. The coalition has endorsed the legislation. In addition to SNM, the coalition includes the American Association of Physicists in Medicine (AAPM), American College of Radiology (ACR), American Nuclear Society (ANS), American Society of Nuclear Cardiology (ASNC), American Society for Radiation Oncology (ASTRO), Council on Radionuclides and Radiopharmaceuticals (CORAR), Health Physics Society (HPS) and Nuclear Energy Institute (NEI). "Recent closures of nuclear facilities abroad are putting a severe strain on our ability to meet demand for this critical medical isotope," said Michael Graham, M.D., Ph.D., president of SNM. "Congress should take steps to boost production domestically and to ensure that the transition away from using highly enriched uranium in medical isotope production does not further strain supplies. We applaud Congress for taking up this issue and urge the government to act without delay." Mo-99 decays into Technetium-99m (Tc-99m) - a medical isotope used in approximately 16 million nuclear diagnostic imaging procedures annually in the United States. These noninvasive procedures are essential for accurately diagnosing and treating patients with potentially life-threatening conditions such as cancer, heart disease and neurologic conditions. Currently, more than 90 percent of Mo-99 is produced in aging nuclear reactors located in Canada, the Netherlands, Belgium, France and South Africa. Concerns about medical isotope supplies have mounted in recent years as scheduled and unplanned shutdowns of overseas reactors have interrupted production. Most recently, the National Research Universal reactor in Ontario, Canada - which supplies about 40 percent of the world"s Mo-99 - has been shut down until later this year because of a heavy water leak following a power outage. Further complicating the situation are recent recommendations to curtail the use of HEU in radionuclide production because of potential security concerns. However, the conversion to the alternative low-enriched uranium (LEU) to produce medical isotopes is still years away. Before such a transition can take place, large-scale commercial facilities must be planned, converted and demonstrate efficacy. To address these concerns, the coalition"s white paper recommends that the government explore a public-private partnership to speed the availability of Mo-99 and ensure continued diagnostic imaging for patients. It is imperative that domestic s of Mo-99 be developed to guarantee a reliable supply. The paper identifies two potential domestic s of Mo-99 as the most viable: the University of Missouri Research Reactor Center (MURR) in Columbia, Mo., and the collaborative effort between the companies Babcock & Wilcox (B&W) and Covidien to build a reactor running strictly on LEU. MURR could meet approximately 50 percent of the U.S. demand for Mo-99 with little change, the paper notes, and it could also help fill gaps in supplies during planned shutdowns of other reactors. B&W and Covidien estimate that a new reactor technology could be operational in about five years and supply half of the U.S. demand for Mo-99. Together, these two s could eventually meet 100 percent of the U.S. demand for Mo-99. The coalition urges the government to speed approvals for these facilities and support the Markey bill, which provides federal funding for the projects. Finally, the organizations stress that any requirement to transition from HEU to LEU in the production of medical isotopes must ensure that supplies of Mo-99 are sufficient and that patient needs are not compromised. Adequate time must be available for research and development to guarantee that the technology and equipment are robust and reliable. Amy Shaw Society of Nuclear Medicine


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