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CGXP SEC Suspension:
http://www.sec.gov/litigation/suspensions/2013/34-70454.pdf
Order:
http://www.sec.gov/litigation/suspensions/2013/34-70454-o.pdf
Admin Proceeding:
http://www.sec.gov/litigation/admin/2013/34-70455.pdf
Someone manipulated the price down 70% by selling just 100 shares at
the bid .003! The ask 0.01 is the recently created new 52-week high!
Only 18M shares OS or $180K low MV at $0.01! What do you mean BTW?
what does this company have on the burner? tried to find something recent and there really is very little info about them...figured i'd throw it out here as i start my DD to see if someone already had their finger on it you know.
IMO, it is a natural bounce due to extremely oversold & undervalued!
what's the deal here? if someone wouldnt mind filling me in...
20K-0.0037 x 10K-0.01 now.
0.0036 x 0.01 now. Only 10K shares left at 0.01!
0.0032 x 0.01 now. The next ask is 0.038!
0.0031 x 0.01 now.
0.003 x 0.01 now. The recent high 0.01 should be easily broken out!
0.003 x 0.006 now. Yesterday it hit the new high 0.01...
0.003 x 0.0059 now. Why someone sold the cheap shares at 0.003 now?
Up strongly so far! 0.01 just hit! 0.004 x 0.01 now.
0.0011 x 0.0015 now. The bid is up 10% so far!
Up 50% now! Bottomed out at all time low 0.001! Extremely oversold!!
It is up 400% today! Easy 10-bagger! Only 18,303,293 shares tiny OS!
Ceragenix and Davi Enter Into Distribution and Supply Agreement for EpiCeram(R)
Davi to Register, Distribute and Market in Europe.
May 19, 2009 7:00:00 AM
Copyright Business Wire 2009
Email Story Discuss on ZenoBank
View Additional ProfilesDENVER--(BUSINESS WIRE)-- Ceragenix Pharmaceuticals, Inc.("Ceragenix") (OTCBB:CGXP), a medical device company focused on infectious disease and dermatology today announced that it has entered into an exclusive distribution and supply agreement (the "Agreement") with Davi II - Farmaceutica S.A., a Portuguese company, ("Davi "), to commercialize EpiCeram(R), a topical cream for treating atopic dermatitis and other dry skin conditions in Europe (the "Territory"). The Agreement grants Davi exclusivity in the Territory for the distribution and marketing of EpiCeram(R) via its own sales force as well as through partnering arrangements. Ceragenix will be responsible for the manufacturing and supply of the product. Davi is also responsible for obtaining regulatory clearance to market EpiCeram(R) in the Territory. Financial terms were not disclosed.
Steven Porter Chairman and Chief Executive Officer of Ceragenix said, "We are delighted to expand our distribution network for EpiCeram(R) by entering this large and promising market with Davi. We look forward to working with Davi in establishing a strong distribution network in Europe in support of this promising new non-steroidal therapy for patients suffering from atopic dermatitis."
Rui P. Rodrigues, Executive Director of Davi, said, " EpiCeram fits perfectly with our company's mission, which is to bring the best, novel innovative treatment to our patients. We are pleased to combine the outstanding medical device development expertise of Ceragenix to Davi's own expertise in marketing and sales. In terms of partnership with Ceragenix we are sure that we will have more complementary business in the future."
About EpiCeram(R)
EpiCeram(R) is a topical cream that utilizes Ceragenix's Barrier Repair Technology. In April 2006, the FDA provided clearance to market EpiCeram(R) to improve dry skin conditions and to relieve and manage the burning and itching associated with various dermatoses including atopic dermatitis (eczema), irritant contact dermatitis, radiation dermatitis, and other dry skin conditions by maintaining a moist wound and skin environment. All of these conditions are associated with a deficient skin barrier function.
About Ceragenix
Ceragenix Pharmaceuticals, Inc. is a medical device company focused on infectious disease and dermatology. The Company has two base technology platforms; Ceragenins(TM) for treatment of infectious disease and Barrier Repair for the treatment of dermatological disorders including atopic dermatitis, neonatal skin disorders and others. Ceragenin(TM) compounds are active against a broad range of gram positive and negative bacteria. We have used our Ceragenin(TM) technology to formulate Cerashield(TM) antimicrobial coatings for medical devices. All Ceragenin(TM) and Cerashield(TM) products are currently in the developmental stage. Ceragenix's patented Barrier Repair technology, invented by Dr. Peter Elias, is the platform for the development of EpiCeram(R) which is currently being marketed by Promius Pharmaceuticals (a wholly owned subsidiary of Dr. Reddy's Laboratories) in the United States under an exclusive supply and distribution agreement. For additional information on Ceragenix, please visit www.ceragenix.com.
About Davi II -Farmaceutica: Davi II -Farmaceutica, S.A. is a pharmaceutical company focused on ophthalmology and dermatology. Davi - Farmaceutica is a laboratory that dates back almost a hundred years. We can trace the company back to its origins in 1915 in Lisbon. Since the beginning, the product portfolio in the areas of ophthalmology and dermatology has grown, firmly believing in the potential for ophthalmic and dermatological products with the Davi brand name. In the beginning of 2008, Davi was acquired by a Portuguese group undergoing expansion, which decided that the Davi name and product portfolio was another innovative project worth investing in, and the new Davi II - Farmaceutica was born. This is another stake in the future, and a very promising one for this group in that it expands its new commercial area sector. For additional information on Davi II, please visit www.davi.pt . Davi, through the excellence of its products and services, would like to play a leading role in the pharmaceutical sector and, keeping abreast of bioeconomical development, make a significant contribution to the realization of its partners' aims.
FORWARD LOOKING STATEMENTS FOR CERAGENIX.
This press release may contain forward-looking statements. These forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those expressed or implied by such forward-looking statements, including, but not limited to, the following: the ability of Davi to successfully obtain marketing clearance for EpiCeram(R) in the EU, the ability of Davi to successfully negotiate distribution agreements with partners in certain countries, the ability of the Company to raise sufficient capital to finance its operations and planned activities including completing development of its Ceragenin(TM) technology; the ability of the Company to meet its obligations under the supply and distribution agreement with Dr. Reddy's Laboratories including having sufficient working capital to fulfill purchase orders within the timeframes required by the agreement; the ability of the Company to service its outstanding convertible debt obligations; receiving the necessary marketing clearance approvals from the United States Food and Drug Administration (the "FDA"); successful clinical trials of the Company's planned products including the ability to enroll the studies in a timely manner, patient compliance with the study protocol, and a sufficient number of patients completing the studies; the ability of the Company to commercialize its planned products; the ability of the Company to successfully manufacture its products in commercial quantities (through contract manufacturers); market acceptance of the Company's planned products, the Company's ability to successfully develop its licensed compounds, alone or in cooperation with others, into commercial products, the ability of the Company to successfully prosecute and protect its intellectual property, general economic conditions in the United States and elsewhere, and the Company's ability to hire, manage and retain qualified personnel. The aforementioned factors do represent an all inclusive list. Actual results, performance or achievements could differ materially from those contemplated, expressed or implied by the forward-looking statements contained in this press release. In particular important factors that could cause actual results to differ materially from our forward-looking statements including general economic factors, business strategies, the state of capital markets, regulatory conditions, and other factors not currently known to us, may be significant, now or in the future, and the factors set forth in this press release may affect us to a greater extent than indicated. All forward-looking statements attributable to us or persons acting on our behalf are expressly qualified in their entirety by the cautionary statements set forth in this press release and in other documents that we file from time to time with the Securities and Exchange Commission including its Annual Report on Form 10-K for the year ended December 31, 2008, Quarterly Reports on Form 10-Q and Current Reports on Form 8-K to be filed in 2009. Except as required by law, we do not undertake any obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise.
Source: Ceragenix Pharmaceuticals, Inc.
----------------------------------------------
Ceragenix Pharmaceuticals
Inc.
Steven Porter
+1-720-946-6440
Chairman and CEO
Ceragenix Enters into Second Exclusive Option to License Agreement for Antimicrobial Medical Device
May 11, 2009 7:00:00 AM
Copyright Business Wire 2009
Email Story Discuss on ZenoBank
View Additional ProfilesDENVER--(BUSINESS WIRE)-- Ceragenix Pharmaceuticals, Inc.("Ceragenix") (OTCBB:CGXP), a medical device company focused on infectious disease and dermatology, today announced that it has entered into an exclusive evaluation and option to license agreement (the "Agreement") with a global, multi-billion dollar healthcare company covering the use of the Company's Cerashield(TM) antimicrobial technology for a specific medical device associated with a high incidence of hospital acquired infections. For competitive reasons, neither the name of the company nor the precise area of interest is being publicly disclosed. Under the terms of the Agreement, the company will have an exclusive period to evaluate, negotiate commercialization terms and license the specified product application for a period of up to seven months. This is the second such agreement entered into by Ceragenix for a medical device application of its CeraShield(TM) antimicrobial technology.
Mr. Steven Porter, Chairman and CEO of Ceragenix said: "We're very pleased to announce our second development agreement involving our CeraShield(TM) antimicrobial coating technology. We believe that attracting a company of this magnitude and caliber is a validation of the potential of our technology."
About Ceragenix
Ceragenix Pharmaceuticals, Inc. is a medical device company focused on infectious disease and dermatology. The Company has two base technology platforms; Ceragenins(TM) for treatment of infectious disease and Barrier Repair for the treatment of dermatological disorders including atopic dermatitis, neonatal skin disorders and others. Ceragenin(TM) compounds are active against a broad range of gram positive and negative bacteria. We have used our Ceragenin(TM) technology to formulate Cerashield(TM) antimicrobial coatings for medical devices. All Ceragenin(TM) and Cerashield(TM) products are currently in the developmental stage. Ceragenix's patented Barrier Repair technology, invented by Dr. Peter Elias, is the platform for the development of EpiCeram(R) which is currently being marketed by Promius Pharmaceuticals (a wholly owned subsidiary of Dr. Reddy's Laboratories) in the United States under an exclusive supply and distribution agreement. For additional information on Ceragenix, please visit www.ceragenix.com.
FORWARD LOOKING STATEMENTS FOR CERAGENIX.
This press release may contain forward-looking statements. These forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those expressed or implied by such forward-looking statements, including, but not limited to, the following: the ability of our partner to successfully develop a product using the Cerashield(TM) technology, the ability to successfully negotiate license terms if a product is successfully developed by our partner, the ability of the Company to raise sufficient capital to finance its operations and planned activities including completing development of its Ceragenin(TM) technology; the ability of the Company to meet its obligations under the supply and distribution agreement with Dr. Reddy's Laboratories including having sufficient working capital to fulfill purchase orders within the timeframes required by the agreement; the ability of the Company to service its outstanding convertible debt obligations; receiving the necessary marketing clearance approvals from the United States Food and Drug Administration (the "FDA"); successful clinical trials of the Company's planned products including the ability to enroll the studies in a timely manner, patient compliance with the study protocol, and a sufficient number of patients completing the studies; the ability of the Company to commercialize its planned products; the ability of the Company to successfully manufacture its products in commercial quantities (through contract manufacturers); market acceptance of the Company's planned products, the Company's ability to successfully develop its licensed compounds, alone or in cooperation with others, into commercial products, the ability of the Company to successfully prosecute and protect its intellectual property, general economic conditions in the United States and elsewhere, and the Company's ability to hire, manage and retain qualified personnel. The aforementioned factors do represent an all inclusive list. Actual results, performance or achievements could differ materially from those contemplated, expressed or implied by the forward-looking statements contained in this press release. In particular important factors that could cause actual results to differ materially from our forward-looking statements including general economic factors, business strategies, the state of capital markets, regulatory conditions, and other factors not currently known to us, may be significant, now or in the future, and the factors set forth in this press release may affect us to a greater extent than indicated. All forward-looking statements attributable to us or persons acting on our behalf are expressly qualified in their entirety by the cautionary statements set forth in this press release and in other documents that we file from time to time with the Securities and Exchange Commission including its Annual Report on Form 10-K for the year ended December 31, 2008, Quarterly Reports on Form 10-Q and Current Reports on Form 8-K to be filed in 2009. Except as required by law, we do not undertake any obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise.
Source: Ceragenix Pharmaceuticals, Inc.
----------------------------------------------
Ceragenix Pharmaceuticals
Inc.
Steven Porter
+1-720-946-6440
Chairman and CEO
Ceragenix Achieves 200 Days of Antimicrobial Efficacy on Treated Silicone Medical Device
May 4, 2009 7:00:00 AM
Copyright Business Wire 2009
Email Story Discuss on ZenoBank
View Additional ProfilesDENVER--(BUSINESS WIRE)-- Ceragenix Pharmaceuticals, Inc. (OTCBB:CGXP) (the "Company"), a medical device company focused on infectious disease and dermatology, today announced that preclinical testing of a silicone medical device incorporating the Company's CeraShield(TM) antimicrobial technology has achieved 200 days of continuous antimicrobial efficacy. The prototype device being tested is an intravaginal silicone ring. Antimicrobial intravaginal rings may be of potential benefit in preventing transmission of certain sexually transmitted diseases. The Company had previously announced when it had achieved 120 days of continuous efficacy in the same study.
This recent testing was focused on urinary tract infections. The testing methodology involved soaking the device in artificial urine with a fresh inoculum of at least 1,000 colony forming units ("CFUs") per ml of E. coli on a daily basis. E. coli is a bacterial pathogen that is the most common cause of urinary tract infections. Millions of silicone urinary catheters are used annually and such devices are associated with high infection rates. It is estimated that of the 2 million hospital acquired infections that afflict patients each year in the United States, 900,000 are urinary tract infections. Of those, approximately 80% are linked to the use of urinary catheters.
The Company is working on incorporating the CeraShield(TM) technology into silicone based urinary catheters, among other ongoing projects. The antimicrobial efficacy testing is being conducted by Dr. Paul B. Savage's laboratory at Brigham Young University ("BYU"). Dr. Savage is the inventor of the Ceragenin(TM) technology, which is exclusively licensed by BYU to the Company.
Steve Porter, Chairman and CEO of Ceragenix stated: "We believe that achieving 200 days of antimicrobial efficacy in this rigorous testing of daily exposure to E. coli is a significant accomplishment. We are actively exploring ways to expand upon this promising finding by developing CeraShield(TM) formulations designed for use with in-dwelling medical devices made from a variety of materials. There are many potential commercial opportunities for use of the CeraShield(TM) technology in providing long lasting antimicrobial protection for in-dwelling medical devices, and we are currently in discussions with potential licensing partners for selected applications of the CeraShield(TM) technology."
About Ceragenix
Ceragenix Pharmaceuticals, Inc. is a medical device company focused on infectious disease and dermatology. The Company has two base technology platforms; Ceragenins(TM) for treatment of infectious disease and Barrier Repair for the treatment of dermatological disorders including atopic dermatitis, neonatal skin disorders and others. Ceragenin compounds are active against a broad range of gram positive and negative bacteria. We have used our Ceragenin technology to formulate Cerashield(TM) antimicrobial coatings for medical devices. All Ceragenin and Cerashield(TM) products are currently in the developmental stage. Ceragenix's patented Barrier Repair technology, invented by Dr. Peter Elias, is the platform for the development of EpiCeram(R) which is currently being marketed by Promius Pharmaceuticals (a wholly owned subsidiary of Dr. Reddy's Laboratories) in the United States under an exclusive supply and distribution agreement. For additional information on Ceragenix, please visit www.ceragenix.com.
FORWARD LOOKING STATEMENTS FOR CERAGENIX.
This press release may contain forward-looking statements. These forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those expressed or implied by such forward-looking statements, including, but not limited to, the following: the ability of the Company to successfully develop a product using the Cerashield(TM) technology, the ability of the Company to raise sufficient capital to finance its operations and planned activities including completing development of its Ceragenin technology; the ability of the Company to meet its obligations under the supply and distribution agreement with Dr. Reddy's Laboratories including having sufficient working capital to fulfill purchase orders within the timeframes required by the agreement; the ability of the Company to service its outstanding convertible debt obligations; receiving the necessary marketing clearance approvals from the United States Food and Drug Administration (the "FDA"); successful clinical trials of the Company's planned products including the ability to enroll the studies in a timely manner, patient compliance with the study protocol, and a sufficient number of patients completing the studies; the ability of the Company to commercialize its planned products; the ability of the Company to successfully manufacture its products in commercial quantities (through contract manufacturers); market acceptance of the Company's planned products, the Company's ability to successfully develop its licensed compounds, alone or in cooperation with others, into commercial products, the ability of the Company to successfully prosecute and protect its intellectual property, general economic conditions in the United States and elsewhere, and the Company's ability to hire, manage and retain qualified personnel. The aforementioned factors do represent an all inclusive list. Actual results, performance or achievements could differ materially from those contemplated, expressed or implied by the forward-looking statements contained in this press release. In particular important factors that could cause actual results to differ materially from our forward-looking statements including general economic factors, business strategies, the state of capital markets, regulatory conditions, and other factors not currently known to us, may be significant, now or in the future, and the factors set forth in this press release may affect us to a greater extent than indicated. All forward-looking statements attributable to us or persons acting on our behalf are expressly qualified in their entirety by the cautionary statements set forth in this press release and in other documents that we file from time to time with the Securities and Exchange Commission including its Annual Report on Form 10-K for the year ended December 31, 2008, Quarterly Reports on Form 10-Q and Current Reports on Form 8-K to be filed in 2009. Except as required by law, we do not undertake any obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise.
Source: Ceragenix Pharmaceuticals, Inc.
----------------------------------------------
Ceragenix Pharmaceuticals
Inc.
Steven Porter
+1-720-946-6440
Chairman and CEO
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Promius Pharma LLC launches new product
Oct 15, 2008 (M2 EQUITYBITES via COMTEX) -- Ceragenix Pharmaceuticals Inc (OTCBB:CGXP), a medical device company focussed on infectious disease and dermatology, said on 14 October that Promius Pharma LLC, a wholly owned subsidiary of Dr. Reddy's Laboratories (DRL) (NYSE: RDY), has launched its first product, EpiCeram Skin Barrier Emulsion, at the 27th Annual Fall Clinical Dermatology Conference. In November 2007, Ceragenix signed an exclusive distribution and supply agreement with DRL for the commercialisation of EpiCeram in the United States. Ceragenix is responsible for the manufacture and supply of the product, while DRL is responsible for the distribution, marketing and sales.
EpiCeram Emulsion is reported to be a novel prescription therapy for the treatment of atopic dermatitis, a skin disease that affects more than 15 million Americans at an estimated cost of USD1bn annually.
(C)2008 M2 COMMUNICATIONS LTD http://www.m2.com
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