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1 <p><b>Researching the Fight Against Infection</b></p>
2 <p>PLIVA is working on becoming a leader in anti-infectives research. As such,
3 current in-house activities are focused predominantly on anti-bacterials; the
4 largest segment of anti-infectives, and in this area, PLIVA has a long tradition
5 and much expertise.</p>
6 <p>With its internationally acknowledged insight into macrolide chemistry, as
7 evidenced by its discovery of Azithromycin, PLIVA has entered into a strategic
8 co-operation with GlaxoWellcome (with the merger of SmithKline and Glaxo a novel
9 Joint Operating Committee is currently being set up) to identify a novel macrolide
10 antibiotic for world-wide development and marketing. The goal of this venture
11 is to identify a macrolide with improved efficacy, particularly against resistant
12 strains of bacteria. The program is currently keeping pace with its ambitious
13 plans and efforts are being focused on fine-tuning the derivation process in
14 order to enter the development phase within the next year.</p>
15 <p align="center"><img src="p/OKrnd_ljudi_7.jpg" width="300" height="202"></p>
16 <p>The goal of a second program within this area is to find a novel anti-bacterial
17 compound class showing no cross-resistance with current antibiotics. In cooperation
18 with Althexis, Boston, USA, a company with leading expertise in structure-based
19 drug design and crystallography, researchers from both companies have identified
20 two novel scaffolds showing activity with in vitro and in vivo models of infections.
21 A derivation program to identify a developmental candidate within the shortest
22 possible time has been fully established.</p>
23 <p>As an extension of its anti-bacterial program, PLIVA has licensed-in a novel
24 anti-fungal compound (PLD-118) from Bayer AG, Germany. This compound has demonstrated
25 excellent efficacy against the most common systemic fungal infections as well
26 as excellent tolerability and pharmacokinetic properties in various pre-clinical
27 models. PLD-118 would represent the first novel, orally available compound class
28 for the treatment of infections caused by the Candida yeast since the introduction
29 of the azoles in the 1970s.The project has a novel mode of action and has strong
30 potential to solve azole resistance problems. </p>

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