Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm

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BIOMODA INC kein aktueller Kurs verfügbar
 
thekey:

Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm

 
07.10.10 13:20
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 8772619images.investorshub.advfn.com/images/...010/2/1/pjcynbmod.jpg" style="max-width:560px" />
Ticker: BMOD
Kurs: $0.17
Börse: OTC BB
Typ of play: Pending News Play
Outstanding shares: 92,006,886
Float: 72,732,809
Webseite: www.biomoda.com
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 8772619stockcharts.com/c-sc/...mp;dy=0&i=p66499891548&r=1657" style="max-width:560px" />
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 8772619ih.advfn.com/...rt&s=NB%5Ebmod&p=0&t=19&vol=1" style="max-width:560px" />
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 8772619realtime.bigcharts.com/...ings=1&rand=7524&mocktick=1" style="max-width:560px" />
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 8772619realtime.bigcharts.com/...ings=1&rand=1652&mocktick=1" style="max-width:560px" />
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 8772619realtime.bigcharts.com/...ings=1&rand=4598&mocktick=1" style="max-width:560px" />

Biomoda anstehenden Daten zu Cypath rücken immer näher

04.10.2010
Global Biotech Investing

Endingen (aktiencheck.de AG) - Sobald die Aktie von Biomoda (ISIN US0906271004 / WKN A0MSTL) anspringt, muss man als Anleger dabei sein, raten die Experten von "Global Biotech Investing".

Bei Biomoda würden die anstehenden Daten zu Cypath immer näher rücken. Bei Cypath handle es sich um ein nicht-invasives Testverfahren zur Früherkennung von Lungenkrebs. Es sei der vielversprechendeste Produktkandidat von Biomoda. Sollte die Phase II-Studie erfolgreich verlaufen, würden die Analysten von LifeTech für Ende des Jahres die Aufnahme einer pivotalen Phase III-Studie erwarten.

Anzeige

Ab 2011 würden die Analysten von LifeTech erstmals Umsätze aus Cypath erwarten. Für 2012 würden sie bei Umsätzen von 3 Mio. USD den Break-even prognostizieren. Für 2013 würden sie dann mit einem Umsatzsprung auf 18 Mio. USD sowie einem Nettogewinn von 10,3 Mio. USD bzw. von 0,08 USD je Aktie rechnen. Damit sei der Titel lediglich mit einem KGV 2013e von 2,5 bewertet.

Bisher sei das Papier vom Markt noch nicht entdeckt worden.

Sobald die Aktie von Biomoda anspringt, muss man als Anleger dabei sein, empfehlen die Experten von "Global Biotech Investing". (Ausgabe 19 vom 04.10.2010) (04.10.2010/ac/a/a)

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thekey:

news

 
07.10.10 16:28
Cancer diagnostics company Biomoda, Inc. (OTC BB: BMOD) today announced in its new monthly President’s Column, posted at www.biomoda.com, that it is extending the pilot clinical trial of its CyPath® diagnostic assay for the detection of early-stage lung cancer to recruit additional participants for the positive control group, patients who have been diagnosed with lung cancer but have not yet begun treatment for the disease.

“The primary purpose of the pilot trial is to assess the specificity and sensitivity of the CyPath® assay and generate sufficient data to move forward with the pivotal clinical trial,” Biomoda President John Cousins said. “The positive control group is critical to assessing the sensitivity of the CyPath® assay. We have had to exclude samples from a significant number of participants in the positive control group from our analysis. Consequently, we plan to add at least one additional enrollment site to expedite recruitment and completion of the study.”

Cousins acknowledged that identifying patients to participate in the positive control group has been a challenge. “It has been difficult to recruit diagnosed pre-treatment patients who are able and willing to give their truly precious time to our study. We thought we had secured sufficient samples, but further investigation showed that some of these lung cancer patients do not fit the FDA-approved criteria for inclusion in the positive control group. Some of the patients’ cancer is located outside the lung cavity. Under the protocol submitted to the FDA, these patients must be excluded from the study,” Cousins said in his President’s Column (posted at www.biomoda.com) updating the status of the clinical trial and other company activities.

“We are still confident the results of our lung cancer pilot study will be more than sufficient to lay the foundation for our pivotal study,” said Cousins.

Biomoda’s CyPath® labeling solution for the early detection of cancers binds to cancer cells and fluoresces under specific frequencies of medium light. Biomoda is seeking Food and Drug Administration (FDA) approval of its cytology-based screening technology as a Class III medical device. Pending FDA approval, CyPath® is for investigational use only.

About Biomoda

Biomoda (www.biomoda.com) is a cancer diagnostics company focused on the development of accurate, inexpensive and noninvasive tests for the early detection of cancer. In addition to its first product for lung cancer, diagnostic assays for cervical, breast, colorectal, bladder, and oral cancers are targeted for development.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are based on estimates, projections, beliefs and assumptions of Biomoda management at the time of such statements and are not guarantees of future performance. Forward-looking statements involve risks and uncertainties in predicting future results and conditions. Actual results could differ materially from those projected in these forward-looking statements due to a variety of factors, including, without limitation, the acceptance by customers of our products, our ability to develop new products cost-effectively, our ability to raise capital in the future, the development by competitors of products using improved or alternative technology, the retention of key employees and general economic conditions. The forward-looking statements contained herein are also subject generally to other risks and uncertainties that are described from time to time in the Company’s reports and registration statements filed with the Securities and Exchange Commission, including those under the heading "Risk Factors" in the Company's Annual Report on Form 10-K filed with the SEC on March 30, 2010. Forward-looking statements are made as of the date of this press release and are subject to change without notice.
MisterDurden:

News

 
07.10.10 17:59
So wie ich das verstehe melden sie ja lediglich, dass sie mehr Versuchspersonen für die Kontrollgruppe benötigen, um den ansprüchen der FDA für eine mögliche Zulassung gerecht zu werden.
Das ist doch insofern, abgesehen von der Verzögerung, doch eigentlich keine schlechte Nachricht, oder seh ich das falsch?

Ein Drittel Kurssturz, wiel sie ihre Arbeit gründlich machen?
Was entgeht mir da?
Sometimes you gotta roll the hard six.
thekey:

Geb Dir Recht

 
07.10.10 23:30
Sehe ich genauso. Börse muss man nicht immer verstehen.
Hier ist noch ein Report nach der News,welcher sehr positiv ausfällt...
BMOD lifetech report
www.lifetechcapital.com/reports/BMOD%20Update%2010-07-10.pdf
MisterDurden:

Einstieg

 
08.10.10 04:13
Hab den Einstieg gewagt und einen Kurs von 0.107 erwischt. Bin gespannt wie es weiter geht ... nicht, dass ich irgendwann noch verbilligen muss ;)
Sometimes you gotta roll the hard six.
thekey:

Zeitplan

 
08.10.10 14:11
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 350097
thekey:

Kursziel

 
08.10.10 14:12
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 350098
thekey:

Drastische Unterbewertung von BMOD

 
08.10.10 14:13
(Verkleinert auf 46%) vergrößern
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 350100
thekey:

Finanzvoschau

 
08.10.10 14:17
(Verkleinert auf 64%) vergrößern
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 350104
thekey:

Einkommenserklärung

 
08.10.10 14:18
(Verkleinert auf 41%) vergrößern
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 350105
thekey:

Aktiva - Passiva

 
08.10.10 14:20
(Verkleinert auf 52%) vergrößern
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 350106
thekey:

Biomoda videos

 
08.10.10 14:42
thekey:

chart intraday

 
08.10.10 14:44
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 8780868
thekey:

FDA Announces Plan To Modernize Regulatory Science

 
08.10.10 14:51
(RTTNews) - The U.S. Food and Drug Administration has announced a plan to spend millions of dollars in order to update its tools for "regulatory science" agenda, which includes reviewing prescription drugs, medical devices and tracking food safety.

The new proposal, titled "Advancing Regulatory Science for Public Health," was released Wednesday by the agency's leaders.

The plan calls for the agency to spend the $25 million allocated within its budget for pilot studies on research in key areas including the use of biomarkers for personalized medicine, better data collection on outcomes for medical devices, and learning how to scientifically assess new technologies in FDA-regulated products.

The agency's total budget is proposed to be $4 billion, but Congress has yet to approve it.

All of the investments are aimed at keeping pace with rapid changes in science and technology.

"We need new approaches, new collaborations and new ways to take advantage of 21st century technologies," the FDA said in its announcement.

"There is no single discovery -- no magic bullet -- to address our unique set of modern scientific regulatory challenges," the agency wrote. "But one thing is clear: if we are to solve the most-pressing public health problems we face today, we need new approaches, new collaborations and new ways to take advantage of 21st century technologies."

by RTT Staff Writer
www.rttnews.com/Content/HealthNews.aspx?Id=1440052&SM=1
thekey:

chart

 
13.11.10 17:50
(Verkleinert auf 68%) vergrößern
Biomoda (BMOD) $0.17 - Ruhe vor dem Sturm 358283
thekey:

news

 
15.11.10 15:45
Cancer diagnostics company Biomoda, Inc. (OTC BB: BMOD) (www.biomoda.com) has allied with Quintiles Global Central Laboratories (www.quintiles.com) to help refine the automated image recognition system for measuring the photon emission rate and cell morphology of CyPath®-stained cells to detect early stage lung cancer.

“One of the key prerequisites prior to commercialization is a highly accurate, fully automated system for reading the assay with state-of-the-art digital technology,” Biomoda President John Cousins said. “Quintiles is the perfect partner for us as we develop our own expert system of digital cytopathology for cancer cell identification. Their in-house pathology capabilities and expertise in tissue-based testing are second to none.”

“We look forward to harnessing innovative pathology and digital technologies with Biomoda to streamline and improve the selection of cancer patients in the New Health,” said Christopher Ung, Vice President, Strategic Business & Operations, Oncology, Quintiles. “Quintiles is committed to alliances that support advances in personalized medicine and the development of safer, more effective targeted therapies.”

Biomoda’s CyPath® labeling solution for the early detection of cancers binds to cancer cells and fluoresces under specific frequencies of medium light. Biomoda is seeking Food and Drug Administration (FDA) approval of its cytology-based screening technology as a Class III medical device. Pending FDA approval, CyPath® is for investigational use only.

Under the terms of the agreement, Quintiles will review CyPath®-stained slides and pap-stained slides to analyze the cell matrices and help Biomoda further calibrate the “signature” of cancer and other aberrant cells that have been labeled with the CyPath® solution.

Quintiles develops proprietary and novel biomarker tests for analyzing genes and proteins that affect cancer cell growth and mutation, and performs these assays at labs in the United States, Scotland and China. Quintiles has the largest and now entirely CAP-accredited central laboratory network in the world, with wholly owned facilities in the United States, Europe, South Africa, India, China, Singapore and Japan, and a tightly controlled network of affiliate laboratories in Argentina and Brazil.

About Biomoda

Biomoda (www.biomoda.com) is a cancer diagnostics company focused on the development of accurate, inexpensive and noninvasive tests for the early detection of cancer. In addition to its first product for lung cancer, diagnostic assays for cervical, breast, colorectal, bladder, and oral cancers are targeted for development.

About Quintiles

Quintiles is the only fully integrated biopharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. The Quintiles network of more than 20,000 engaged professionals in 60 countries works with an unwavering commitment to patients, safety and ethics. Quintiles helps biopharmaceutical companies navigate risk and seize opportunities in an environment where change is constant. For more information, please visit www.quintiles.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are based on estimates, projections, beliefs and assumptions of Biomoda management at the time of such statements and are not guarantees of future performance. Forward-looking statements involve risks and uncertainties in predicting future results and conditions. Actual results could differ materially from those projected in these forward-looking statements due to a variety of factors, including, without limitation, the acceptance by customers of our products, our ability to develop new products cost-effectively, our ability to raise capital in the future, the development by competitors of products using improved or alternative technology, the retention of key employees and general economic conditions. The forward-looking statements contained herein are also subject generally to other risks and uncertainties that are described from time to time in the Company’s reports and registration statements filed with the Securities and Exchange Commission, including those under the heading "Risk Factors" in the Company's Annual Report on Form 10-K filed with the SEC on March 30, 2010. Forward-looking statements are made as of the date of this press release and are subject to change without notice.
MisterDurden:

Einstieg

 
09.12.10 20:17
Was meint ihr: ist das nicht ein guter Kurs zum Einstieg, bzw. für die, die schon drin sind, ein guter Kurs zum verbilligen? Die 10cent scheinen ja mehr oder weniger zu halten
Sometimes you gotta roll the hard six.
xnomis:

Das Teil ist fast so süß wie meine kleine :)

 
09.03.11 12:13
diesen Monat endgültige Präsentation der PhaseII Ergebnisse, sowie Start des III Trials.
Ziel 0,75$ - 1,5$
xnomis:

der Kurs hat die letzten Tag super angezogen.

 
29.03.11 21:02
Veröffentlichung der Phase II Zahlen heute oder morgen.
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