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	<title>BioHorizon &#187; Nabi Pharmaceutical</title>
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	<description>Emerging Health Technology Surveillance and Analysis</description>
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		<title>Xenova Group&#8217;s TA-NIC for the Treatment of Nicotine Addiction</title>
		<link>http://www.biohorizon.com/2004/07/xenova-groups-ta-nic-for-the-treatment-of-nicotine-addiction/</link>
		<comments>http://www.biohorizon.com/2004/07/xenova-groups-ta-nic-for-the-treatment-of-nicotine-addiction/#comments</comments>
		<pubDate>Wed, 14 Jul 2004 21:00:24 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Drug]]></category>
		<category><![CDATA[Medicine]]></category>
		<category><![CDATA[Nervous]]></category>
		<category><![CDATA[Acomplia]]></category>
		<category><![CDATA[Addictions]]></category>
		<category><![CDATA[Nabi Pharmaceutical]]></category>
		<category><![CDATA[Nervous System]]></category>
		<category><![CDATA[nicotine addiction]]></category>
		<category><![CDATA[NicVax]]></category>
		<category><![CDATA[Phase I]]></category>
		<category><![CDATA[Sanofi]]></category>
		<category><![CDATA[Smoking Cessation]]></category>
		<category><![CDATA[TA-NIC]]></category>
		<category><![CDATA[therapeutic vaccine]]></category>
		<category><![CDATA[Xenova Group]]></category>

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		<description><![CDATA[On July 14, 2004 Xenova Group plc released results of a second clinical trial with TA-NIC, a therapeutic vaccine under development for the treatment of nicotine addiction. The company reported that this randomized, placebo controlled, double-blinded study involved a total of 60 smokers and was designed to prove safety and tolerability data while measuring anti-nicotine [...]]]></description>
			<content:encoded><![CDATA[<p>On July 14, 2004 Xenova Group plc released results of a second clinical trial with TA-NIC, a therapeutic vaccine under development for the treatment of nicotine addiction. The company reported that this randomized, placebo controlled, double-blinded study involved a total of 60 smokers and was designed to prove safety and tolerability data while measuring anti-nicotine antibody response in participants. The company reported no serious adverse events and indicated that anti-nicotine antibody levels were dose dependent. Although not an efficacy trial, 43% of smokers receiving TA-NIC either gave up smoking or reported a decrease in smoking related pleasure compared to 9% in the placebo group.</p>
<p>Nicotine by itself does not induce an antibody or immune response. However, when conjugated with an immunogenic protein such as recombinant cholera protein, an immune response is generated. These anti-nicotine antibodies may bind to the nicotine in a smoker’s blood and decrease or reduce the positive effects that nicotine creates in the smoker. In the Phase I trial, TA-NIC was delivered by 5 vaccinations over 8-20 weeks with a booster given 9 months after the first injection.</p>
<p>According to the 2001 National Health Interview Survey, approximately 22.8% of American adults (46.2 million) are currently smokers. Smoking rates in the United States have been declining since 1965.</p>
<p>The Biohorizon Emerging Health Technology Database contains two other emerging technologies for the treatment of Nicotine Addiction/Smoking Cessation, NicVax and Acomplia™. Notably, Nabi Pharmaceutical’s NicVax is another Phase I therapeutic vaccine, while Sanofi’s Acomplia™ is a Phase III drug therapy under development for both obesity and smoking cessation.  </p>
<p>TA-NIC is an early stage therapeutic vaccine for smoking cessation with interesting Phase I trial results and substantial obstacles in the form of pivotal Phase 3 trials to overcome. We currently recommend no assessment activities for health services clients at this time.</p>
<p><strong>Technology Details</strong><br />
Target Disease / Indication: Smoking Cessation/Nicotine Addiction<br />
Technology Classification: Drug<br />
Body System: Nervous System<br />
Program Area: Medicine/Addictions<br />
Regulatory Status: Phase I<br />
BioHorizon Impact Score: 53/100 – Moderate</p>
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