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	<title>BioHorizon &#187; NX-1207</title>
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	<description>Emerging Health Technology Surveillance and Analysis</description>
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		<title>Nymox Pharmaceutical NX-1207 for BPH</title>
		<link>http://www.biohorizon.com/2004/07/nymox-pharmaceutical-nx-1207-for-bph/</link>
		<comments>http://www.biohorizon.com/2004/07/nymox-pharmaceutical-nx-1207-for-bph/#comments</comments>
		<pubDate>Wed, 14 Jul 2004 21:03:51 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Drug]]></category>
		<category><![CDATA[Genitourinary]]></category>
		<category><![CDATA[Medicine]]></category>
		<category><![CDATA[benign prostatic hyperplasia]]></category>
		<category><![CDATA[Benign Prostatic Hypertrophy]]></category>
		<category><![CDATA[BPH]]></category>
		<category><![CDATA[Genitourinary System]]></category>
		<category><![CDATA[lemuteporfin]]></category>
		<category><![CDATA[NX-1207]]></category>
		<category><![CDATA[Nymox Pharmaceutical]]></category>
		<category><![CDATA[QLT]]></category>
		<category><![CDATA[TURP]]></category>
		<category><![CDATA[Urology]]></category>

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		<description><![CDATA[On July 14, 2004 Nymox Pharmaceutical Corporation reported FDA approval for the NX-1207 clinical trial protocol for benign prostatic hyperplasia (BPH). In January 2004 the company had reported Phase I results which indicated that safety and tolerability data were sufficient for the company to move NX-1207 into Phase II testing. The recent FDA ruling has [...]]]></description>
			<content:encoded><![CDATA[<p>On July 14, 2004 Nymox Pharmaceutical Corporation reported FDA approval for the NX-1207 clinical trial protocol for benign prostatic hyperplasia (BPH). In January 2004 the company had reported Phase I results which indicated that safety and tolerability data were sufficient for the company to move NX-1207 into Phase II testing. The recent FDA ruling has allowed Nymox to commence Phase II testing. Nymox has released limited clinical trial data; however, according to press releases, the drug has shown significant clinical improvement including statistically significant prostate shrinkage.</p>
<p>According to Bandolier, approximately half of all men have histological evidence of BPH at age 60, a number that increases to 90% by age 85. About 25% of American men will be treated for BPH by the time they reach 80. About 300,000 surgical procedures are performed each year for BPH. Most of these are transurethral resections of the prostate (TURP), making TURP the second most common surgical procedure next to cataracts at a cost estimated at $2 billion per year. Available medical therapies include treatment using alpha-1-adrenergic receptor blockers that inhibit contraction of prostatic smooth muscle, and treatment using a 5-alpha reductase inhibitor (finasteride), an enzyme inhibitor that lowers prostatic androgen levels and can result in some decreased prostate size.</p>
<p>The Biohorizon Emerging Health Technology Database currently lists two other therapies under development for BPH. QLT’s lemuteporfin is the only molecule under active evaluation. The potential large market size for a breakthrough therapy in BPH makes ongoing developments in this area important. However, NX-1207 must succeed in Phase II and enter pivotal Phase III studies before we would advise health services clients to commence assessment activities. Note that due to the lack of information supplied by Nymox regarding NX-1207, we are unable to discuss the structure and function of this drug in any detail. In our impact assessment, the innovation variable was therefore assigned the default value of 50 (new molecule in an existing class).  </p>
<p><strong>Technology Details</strong><br />
Target Disease / Indication: Benign Prostatic Hypertrophy<br />
Technology Classification: Drug<br />
Body System: Genitourinary System<br />
Program Area: Urology<br />
Regulatory Status: Phase II<br />
BioHorizon Impact Score: 53/100 – Moderate</p>
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