LA JOLLA - heute mit kräftigem Rebound?
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Eröffnet am: | 19.02.03 14:11 | von: Pavian1 | Anzahl Beiträge: | 43 |
Neuester Beitrag: | 20.04.10 17:34 | von: Bersch1986 | Leser gesamt: | 8.357 |
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Die Ergebnisse für das Medikament seien nicht so schlecht, wie dies der Kursrückgang vermuten liese, so die Analysten von Fulcrum. Das Medikament diene zur Behandlung einer bislang nicht sinnvoll therapierbaren Krankheit, hieß es. Auch habe das Testverfahren keine Sicherheitsrisiken des Medikamentes aufgezeigt. Sollte ein weiterer Testdurchlauf von Nöten sein, so wird dies vom Unternehmen finanziert werden können, so Fulcrum weiter. Die Analysten haben ein Kursziel von $26.
Denke nach dem Kursverfall gestern geht es heute einige % nach oben!! Ist noch jemand dabei??
Grüße
Pavian
XOMA, ONXX, etc. etc. Auch am Neuen Markt waren das die heissesten Eisen letztes
Jahr. Legendär fand ich Star Ikones Einstieg bei Curasan und Codon, jeweils 300% mit Ansage, Morphosys, Lion B.s und Biolitecs Sprünge unvergessen.
Fazit, wer La Jolla nicht bald einsammelt....
Werde meinen Einstieg posten.
Gruss E.
Werden die noch weiter fallen?
Danke im vorraus für Deine Antwort!
Heute spricht La Jolla übrigens auf einem Biotech-Kongress vor, vielleicht kommen im Laufe des Tages noch News..
Pavian
Ich hab mal ganz konservativ ein paar Avocent, grösster russischer Autobauer für 28 Dollar und Zimmer Holdings für 45 Dollar eingeschoben, haben beide heute Ihr ATH geknackt.
Gruss E.
was denn nun???
Na immerhin kam Widerspruch, hat mal einer aufgepast.
Gruss E.
Konferenz gestern lief (positiver Ausblick?)!
La Jolla Pharmaceutical Company is a biotechnology company developing therapeutics for antibody-mediated autoimmune diseases afflicting several million people in the United States and Europe. The Company is developing Riquent(TM) for the treatment of lupus kidney disease, a leading cause of sickness and death in patients with lupus. The Company is also developing LJP 1082 for the treatment of antibody-mediated thrombosis, a condition in which patients suffer from recurrent stroke, deep-vein thrombosis and other thrombotic events. The Company's common stock is traded on The Nasdaq Stock Market under the symbol LJPC. For more information about the Company, visit our Web site: http://www.ljpc.com .
Except for historical statements, this press release contains forward-looking statements involving significant risks and uncertainties, and a number of factors, both foreseen and unforeseen, could cause actual results to differ materially from our current expectations. Forward-looking statements include those, which express a plan, belief, expectation, estimation, anticipation, intent, contingency, future development or similar expression. Although we expect to meet with the U.S. Food and Drug Administration ("FDA") to discuss the results of our Phase III trial of Riquent(TM), there is no guarantee that a meeting with the FDA can be held in a timely manner, or at all, or that our meetings with them will result in us being able to continue to develop Riquent(TM). Our analyses of clinical results of Riquent(TM), previously known as LJP 394, our drug candidate for the treatment of systemic lupus erythematosus ("lupus"), and LJP 1082, our drug candidate for the treatment of antibody-mediated thrombosis ("thrombosis"), are ongoing and could result in a finding that these drug candidates are not effective in large patient populations, do not provide a meaningful clinical benefit or may reveal a potential safety issue requiring us to develop new candidates. Our blood test to measure the binding affinity for Riquent(TM) is experimental, has not been validated by independent laboratories, may require regulatory approval, and may be necessary for the approval and the commercialization of Riquent(TM). Our other potential drug candidates are at earlier stages of development and involve comparable risks. Analysis of our clinical trials could have negative or inconclusive results. Any positive results observed to date may not be indicative of future results. In any event, the FDA may require additional clinical trials, or may not approve our drugs. Our ability to develop and sell our products in the future may be affected by the intellectual property rights of third parties. Additional risk factors include the uncertainty of: obtaining required regulatory approvals, including delays associated with any approvals that we may obtain; FDA approval of our manufacturing facilities and processes; the increase in capacity of our manufacturing capabilities for possible commercialization; successfully marketing and selling our products; our lack of manufacturing, marketing, and sales experience; generating future revenue from product sales or other sources such as collaborative relationships; future profitability; our need for additional financing; and our dependence on patents and other proprietary rights. Readers are cautioned to not place undue reliance upon forward-looking statements, which speak only as of the date hereof, and we undertake no obligation to update forward-looking statements to reflect events or circumstances occurring after the date hereof. Interested parties are urged to review the risks described in our Registration Statement on Form S-3, filed December 10, 2002, our Annual Report on Form 10-K for the year ended December 31, 2001, and in other reports and registration statements that we file with the Securities and Exchange Commission from time to time.
SOURCE La Jolla Pharmaceutical Company
Andrew Wiseman, Ph.D., Sr. Director of Business Development of
La Jolla Pharmaceutical Company, +1-858-646-6615, andrew.wiseman@ljpc.com ;
or media, Virginia Amann or Trista Morrison, tmorrison@irpr.com , both of
Atkins + Associates, +1-858-527-3490, for La Jolla Pharmaceutical Company
http://www.ljpc.com
SAN DIEGO, Mar 4, 2003 /PRNewswire-FirstCall via COMTEX/ -- La Jolla Pharmaceutical Company (Nasdaq: LJPC), reported a net loss for the fourth quarter ended December 31, 2002 of $13.2 million or $0.31 per share (on 42.4 million weighted average shares) compared to a net loss of $6.7 million or $0.19 per share (on 35.3 million weighted average shares) for the fourth quarter of 2001. The net loss for the year ended December 31, 2002 was $43.3 million or $1.03 per share (on 42.0 million weighted average shares) compared to a net loss of $24.7 million or $0.71 per share (on 34.6 million weighted average shares) for the same period in 2001.
Research and development expenses increased to $11.3 million and $37.7 million for the three and twelve months ended December 31, 2002, respectively, compared to $5.9 million and $23.2 million for the comparable periods in 2001. The increase was primarily due to expenses associated with the Phase III clinical trial of Riquent(TM), the Company's lupus drug candidate, which was initiated in September 2000 and completed in December 2002, and the on-going open-label follow-on clinical trial of Riquent(TM), which was initiated in July 2002. The increase was also due to the Phase I/II clinical trial of LJP 1082, the Company's thrombosis drug candidate, which was initiated in November 2001 and completed in October 2002.
Cash, cash equivalents and short-term investments as of December 31, 2002 were $52.7 million compared to $47.0 million as of December 31, 2001. In January 2002, the Company sold 7.0 million shares of its common stock in a private placement for net proceeds of approximately $48.3 million. The Company anticipates that its existing cash, investments and interest earned thereon will be sufficient to fund the Company's operations as currently planned into the first quarter of 2004, assuming that it does not undertake significant commercialization activities for Riquent(TM).
Gruße
Pavian
PS: Gerade mit knapp 4% ins Plus gedreht in New York!
ist um 21.45 Uhr unserer Zeit, viel Auswirkung auf den heutigen Kurs wird es wohl nicht mehr haben, aber aufjedenfall MORGEN!
La Jolla Pharmaceutical Co.(NASDAQ-NMS:LJPC)
§ - San Diego
4th Quar Dec. 31:
2002 2001
Net income $(13,159,000) $(6,682,000)
Avg shrs (diluted) 42,427,000 35,255,000
Shr earns
Net income (.31) (.19)
Year:
Net income (43,318,000) (24,683,000)
Avg shrs (diluted) 42,046,000 34,604,000
Shr earns
Net income (1.03) (.71)
Figures in parentheses are losses.
La Jolla Pharmaceutical Co.(NASDAQ-NMS:LJPC) (LJPC) said research and development expenses grew to $11.3 million in the fourth quarter from $5.9 million a year earlier due to costs related to clincal trials of the company's Riquent lupus drug, as well as its thrombosis drug candidate.
La Jolla had $52.7 million in cash and equivalents at the end of the year, compared with $47 million at the end of 2001.
La Jolla expects to have enough cash for operations through the first quarter of 2004, assuming that it doesn't have significant commercialization for Riquent. In mid-February, La Jolla said that Phase III trials for Riquent didn't meet its primary endpoint.
-Kara Wetzel; Dow Jones Newswires; 201-938-5388
La Jolla Pharma kaufen
Global Biotech Investing
Zum Kauf von einigen Aktien der La Jolla Pharmaceutical Company (WKN 898844) raten die Experten vom Börsenbrief "Global Biotech Investing".
Aufgrund enttäuschender Ergebnisse des Wirkstoffs RIQUENT sei der Wert an einem Tag um 75% in die Tiefe gerauscht und habe in den Folgetagen weitere Verluste hinnehmen müssen. Diese Reaktion halte "Global Biotech Investing" für übertrieben.
Zwar habe das Medikament gegen Morbus Lupus nicht das Ziel der Phase III-Studie erreichen können, dennoch stünden die Chancen auf eine Zulassung durch die FDA nicht schlecht.
Denn bislang könne die Krankheit nicht vollständig geheilt werden und im Gegensatz zu Konkurrenzprodukten erreiche RIQUENT eine größere Linderung der Beschwerden und weise ein weitaus besseres Sicherheitsprofil aus.
Die nächste positive Meldung dürfte den Kurs wieder spürbar ansteigen lassen. Nach dem Kurseinbruch würden UBS Warburg, Morgan Keegan und Fortis den Wert zum Kauf empfehlen.
Eine kleine Startposition mit Aktien von La Jolla Pharma sollten sich interessierte Anleger nach Meinung der Experten von "Global Biotech Investing" ins Depot legen.