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Hemodialyzer Industry Global and Chinese Analysis for 2015-2020 in New ... - MarketWatch PDF Print

DALLAS, April 17, 2015 /PRNewswire via COMTEX/ -- DALLAS, April 17, 2015 /PRNewswire/ --

This report estimates 2015-2020 Hemodialyzer Industry Cost and Profit with Market Competition of Hemodialyzer Industry By Country: (Including Europe, U.S., Japan, China etc.), By Company and Application. Get full report copy athttp://www.rnrmarketresearch.com/2015-hemodialyzer-industry-report-global-and-chinese-market-scenario-market-report.html  .

This Global and Chinese Report 2015 is a result of industry experts' diligent work on researching the world market of Hemodialyzer. The report helps to build up a clear view of the market (scenario and survey), identify major players in the industry, and analyzes the upstream raw materials, downstream clients, and current market dynamics of Hemodialyzer Industry.

This report reviews the basic information of Hemodialyzer including its classification, application and manufacturing technology. This report explores global and China's top manufacturers of Hemodialyzer listing their product specification, capacity, Production value, and market share etc. The report further analyzes quantitatively 2010-2015 global and China's total market of Hemodialyzer by calculation of main economic parameters of each company. The breakdown data of Hemodialyzer market are presented by company, by country, and by application.

In the end, the report makes a proposal for a new project of Hemodialyzer Industry before evaluating its feasibility. Overall, the report provides an in-depth insight of 2010-2015 global and China Hemodialyzer industry covering all important parameters.

Purchase a copy of this report (Global and Chinese Hemodialyzer Industry, 2010-2020 Market Research Report) at  http://www.rnrmarketresearch.com/contacts/purchase?rname=358693  . The first chapter introduces the Hemodialyzer Industry by Brief Introduction, Development & Status of Hemodialyzer Industry.

The second chapter focuses on Manufacturing Technology of Hemodialyzer, the third one gives Analysis of Global Key Manufacturers (Including Company Profile, Product Specification, 2010-2015 Production Information etc.)

The forth chapter deals with 2010-2015 Global and China Market of Hemodialyzer. The chapter 5 summarizes Market Status of Hemodialyzer Industry.

Other Related Report 

The market size of Chinese hemodialysis market exceeded CNY 20 billion in China in 2013 with the annual growth rate of 20%30%. Instruments, drugs and services are three major factors of the hemodialysis market, also the three entry points of the industry chain.

By 2020, the global ESRD patients receiving hemodialysis treatment will reach 4.2 million while that in China will surpass 1 million. The market size of Chinese hemodialysis market is expected to exceed CNY 70 billion in China by 2020 with the CAGR above 20%. Meanwhile, the market size of auxiliary drugs will exceed CNY 60 billion.

Key Enterprises in China Hemodialysis Market, 2011-2014

Fresenius SE & Co. KGaA, Nipro Co.,Ltd., Baxter International, Asahi Kasei Corporation, Weigao Group, Huaren Pharmaceutical Co., Ltd., Guangdong Biolight Meditech Co., Ltd., Sichuan Kelun Pharmaceutical Co., Ltd., Jihua Medical Apparatus and Instruments Co., Ltd., Bain Medical Equipment (Guangzhou) Co., Ltd. 

Place a direct purchase order of this report (Research Report on Hemodialysis Industry in China, 2014-2018) at  http://www.rnrmarketresearch.com/contacts/purchase?rname=212747  .

Hemodialysis (also HD) is one of the replace therapies for patients with acute and chronic renal failure. There are globally 2.2 million uremia patients (end stage renal disease, ESRD) receiving dialysis treatment, including over 89% of them receiving hemodialysis. As the cost of hemodialysis is high, most dialysis patients are concentrated in developed regions like Europe and the U.S. The dialysis patients are fewer in developing countries but increases rapidly. In recent years, the growth rate of dialysis patients in China, India and Brazil remains above 15%, much higher than 3%5% in Europe and the U.S. Meanwhile, the proportion of ESRD patients that receive dialysis treatment is only 10%20% in developing countries, much lower than 80% in Europe and the U.S.A.

As Chinese economy develops with increasing income per capita and payment ability of hemodialysis patients, the industry will develop rapidly in the future. The costs of hemodialysis consist of instruments, drugs and services with the proportions of 45%, 25% and 30% respectively. Hemodialysis instruments include dialysis machines, dialyzer and dialysis pipelines. Dialyzers are core supplies with high technical barriers and account for the largest market shares. The market size in China exceeds CNY 5 billion while the domestic market share is approximately 30%. More domestic products become substitutes of imports. The dialysis machine market is dominated by foreign funded brands, which belong to onetime investment in the earlier stage. Conventional medicines of hemodialysis include EPO and heparin, which are basically domestically produced. Service costs include costs of bed and health care labors. The three major operation modes of domestic private hemodialysis centers include independent hemodialysis centers, cooperation with hospitals and investment in instruments.

Readers can obtain the following information or more through this report: 

  • Status of Hemodialysis Market in China
  • Economic Environment and Policy Environment for China Hemodialysis Market
  • Major Suppliers of Equipment and Consumables in China Hemodialysis Market
  • Competition Status of China Hemodialysis Market
  • Driving Factors for Development of China Hemodialysis Market
  • Forecast on Development of China Hemodialysis Market

The following enterprises and people are recommended to purchase this report: 

  • Medical Institutions
  • Manufacturers of Medical Equipment and Drugs
  • Trading Enterprises of Medical Equipment and Drugs
  • Investors and Research Institutions Concerned about Hemodialysis Market

Browse more reports on "Urology Device" @  http://www.rnrmarketresearch.com/reports/life-sciences/medical-devices/urology-device  .

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Medgenics Reports First Quarter 2015 Financial Results - Nasdaq PDF Print
Nasdaq
Moving forward, we will focus on initiating small proof-of-concept studies in additional renal indications through the remainder of 2015, beginning with the study of end-stage renal disease (ESRD) patients undergoing peritoneal dialysis now underway in

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Medgenics Reports First Quarter 2015 Financial Results - CNNMoney PDF Print
  • Commenced enrollment in mid-dose arm of MDGN-201 study
  • Initiated peritoneal dialysis study in Israel
  • Filed U.S. IND for TARGTEPO renal anemia programs
  • Advanced collaboration activities with CHOP
  • Progressed TARGTCNS program with Harvard University

PHILADELPHIA, April 17, 2015 (GLOBE NEWSWIRE) -- Medgenics, Inc.(NYSE:MDGN) (the Company), the developer of a proprietary platform for the sustained production and delivery of therapeutic proteins and peptides in patients using ex vivo gene therapy and their own tissue for the treatment of orphan diseases, today announced first quarter 2015 financial results.

Management Commentary

"We are very pleased with the considerable progress we have made with our development pipeline for the TARGT (Transduced Autologous Restorative Gene Therapy) platform this quarter," stated Mike Cola, Chief Executive Officer of Medgenics. "We have initiated enrollment in the mid-dose cohort of our MDGN-201 study, and we continue to see promising results validating the TARGT platform in the low-dose cohort, with one patient currently at 10 months post-implantation. We look forward to presenting data from this study at the upcoming American Society of Gene and Cell Therapy (ASGCT) annual meeting in New Orleans in May.

Moving forward, we will focus on initiating small proof-of-concept studies in additional renal indications through the remainder of 2015, beginning with the study of end-stage renal disease (ESRD) patients undergoing peritoneal dialysis now underway in Israel. We filed an investigational new drug (IND) application for MDGN-201 with the FDA this quarter, and expect to initiate our U.S.-based peritoneal dialysis study in the near-term.

Furthermore, the Company is actively advancing our collaboration efforts. We are pleased to announce the hiring of Robert Zivin, Ph.D. to head our translational research activities in connection with our collaboration with Children's Hospital of Philadelphia (CHOP). We are actively working with CHOP to assess and prioritize programs in the collaboration, from which we anticipate announcing a lead program later this year.

Additionally, we are advancing our collaboration with Harvard University that will assess the viability and durability of our TARGT platform for potential applications involving the central nervous system (CNS). We look forward to providing preclinical data from this program in the second half of the year.

And finally, we continue to be opportunistic in considering collaboration and partnership opportunities, and remain diligent in our assessment of potential novel licensing opportunities. We look forward to discussing these results during our first quarter conference call and webcast."

The Company also announced today that all resolutions proposed at the Company's Annual Meeting of Stockholders held yesterday were duly passed.

Dr. Sol J. Barer, Dr. Eugene A. Bauer, Mr. Isaac Blech, Dr. Alastair Clemow, Mr. Michael F. Cola, Mr. Wilbur H. Gantz and Mr. Joseph J. Grano, Jr., were reelected to the Board of Directors. 

Mr. Joel S. Kanter and Dr. Stephen D. McMurray retired from the Board of Directors at the meeting following the expiration of their terms. "On behalf of the Board of Directors and the entire staff at Medgenics, I extend our deepest gratitude to Mr. Kanter and Dr. McMurray for their service to the company," said Sol J. Barer, Non-Executive Chairman of the Board of Medgenics.

Stockholders also ratified the appointment of Kost Forer Gabbay & Kasierer, a member of Ernst & Young Global, to serve as the Company's independent registered public accounting firm for the year ended December 31, 2015.

In connection with the appointment of Robert Zivin, the Compensation Committee of the Medgenics Board of Directors has granted Dr. Zivin inducement awards consisting of stock options covering up to 100,000 shares of the Company's common stock, $0.0001 par value per share (Common Stock), at a per share exercise price of $9.00, representing the closing price of the Common Stock on the grant date. These options have a 10-year term, with one-third of the options vesting on the first anniversary of grant, one-third vesting on the second anniversary, and the final third vesting on the third anniversary of the grant date, subject to Dr. Zivin's continuous service through each vesting date. The Compensation Committee of the Medgenics Board of Directors, which is comprised solely of independent directors, granted this award on April 16, 2015 pursuant to a stand-alone award agreement outside of Medgenics' Stock Incentive Plan as an inducement material to Dr. Zivin's acceptance of his appointment to the company in accordance with Section 711 of the NYSE MKT Company Guide.

Conference Call and Webcast

Medgenics will host a conference call and live audio webcast on Friday, April 17, 2015 at 8:30 a.m. ET to discuss first quarter 2015 financial results.

In order to participate in the conference call, please dial (844) 466-4113 (domestic) or (765) 507-2652 (international). The conference ID number is 18428859.

The live webcast can be accessed under "Events" in the Investors section of the Company's website at www.medgenics.com or you may use the link: http://edge.media-server.com/m/p/9erkq6a8/lan/en .

A replay of the call will be available two hours after the end of the conference on April 17, 2015 through April 24, 2015. To access the replay, please dial (855) 859-2056 (domestic) or (404) 537-3406 (international) and reference the conference ID number.

The archived webcast will be available for 30 days in the Investor section of Medgenics' website at www.medgenics.com.

First Quarter Financial Results

The Company reported financial results for the three months ended March 31, 2015 and the filing with the U.S. Securities and Exchange Commission (SEC) of the Company's Quarterly Report on Form 10-Q. The Form 10-Q includes unaudited interim consolidated financial statements containing the information presented below, as well as additional information regarding the Company. The Form 10-Q is available at www.sec.gov and at www.medgenics.com.

Gross research and development (R&D) expenses for the three months ended March 31, 2015 increased to $3.90 million from $2.14 million for the same period in 2014. This increase was due mainly to increased materials and sub-contractor costs and increased stock-based compensation expenses related to options granted to research and development personnel.

General and administrative expenses for the three months ended March 31, 2015 were $3.95 million, increasing from $3.09 million for the same period in 2014 primarily due to increased stock-based compensation expenses related to options granted to directors and general and administrative personnel, offset in part by a decrease in professional fees.

Financial expenses for the quarters ended March 31, 2015 were $1.08 million, increasing from $0.12 million for the same period in 2014. This increase was mainly due to the change in valuation of the warrant liability.

Financial income for the quarters ended March 31, 2015 and 2014 was de minimis.

The Company reported cash and cash equivalents of $25.16 million as of March 31, 2015.

For the quarter ended March 31, 2015 the Company reported a loss of $8.92 million or $0.36 per share, compared with a loss of $5.36 million or $0.28 per share for the comparative quarter in 2014.

About Medgenics

Medgenics is developing the TARGT (Transduced Autologous Restorative Gene Therapy) system, a proprietary platform for the sustained production and delivery of therapeutic proteins and peptides using ex vivo gene therapy and the patient's own tissue for the treatment of orphan and rare diseases. For more information, visit the Company's website at www.medgenics.com

Forward-looking Statements

This release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, Section 21E of the Securities Exchange Act of 1934 and as that term is defined in the Private Securities Litigation Reform Act of 1995, which include all statements other than statements of historical fact, including (without limitation) those regarding the Company's financial position, its development and business strategy, its product candidates and the plans and objectives of management for future operations. The Company intends that such forward-looking statements be subject to the safe harbors created by such laws. Forward-looking statements are sometimes identified by their use of the terms and phrases such as "estimate," "project," "intend," "forecast," "anticipate," "plan," "planning, "expect," "believe," "will," "will likely," "should," "could," "would," "may" or the negative of such terms and other comparable terminology. All such forward-looking statements are based on current expectations and are subject to risks and uncertainties. Should any of these risks or uncertainties materialize, or should any of the Company's assumptions prove incorrect, actual results may differ materially from those included within these forward-looking statements. Accordingly, no undue reliance should be placed on these forward-looking statements, which speak only as of the date made. The Company expressly disclaims any obligation or undertaking to disseminate any updates or revisions to any forward-looking statements contained herein to reflect any change in the Company's expectations with regard thereto or any change in events, conditions or circumstances on which any such statements are based. As a result of these factors, the events described in the forward-looking statements contained in this release may not occur.

CONTACT: Medgenics, Inc.
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         Medgenics, Inc.
         Brian Piper
         240-899-5554
         
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Genetics Ups Risk of Cardiac Arrest in Dialysis Patients - Medscape PDF Print
Medscape
Heritable factors appear to contribute to the risk for cardiac arrest in patients receiving dialysis, according to a study published online April 16 in the Journal of the American Society of Nephrology. "The discovery of predictive markers for cardiac ...
Genes May Be Tied to Cardiac Arrest Risk in Dialysis Patients HealthDay
Public Release: 16-Apr-2015 Family history increases the risk of cardiac

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Dialysis machines at both govt medical colleges go defunct - Times of India PDF Print
Nagpur: Poor patients of kidney failure requiring dialysis are being put to huge inconvenience at the two government medical colleges as the dialysis machines there are non-functional. They have to either go to a private hospital and pay huge money (over 1,500 per dialysis) or get it done at the Super Specialty Hospital (SSH) which is the lone government facility left offering it and thus over-burdened.

The machines at Government Medical College (GMC) and Indira Gandhi Government Medical College (IGGMC) are non-functional due to failure of the RO (Reverse Osmosis) machine costing about 3 lakh, which is an integral part of the dialysis machine. Sources at IGGMC told TOI that despite having a maintenance contract, the manufacturing company didn't provide service. Since last six months, the college has been tendering for purchasing the machine but has not got a suitable bidder. At GMCH, it seems the problem is both of the RO plant going defunct as well as absence of a technician who can run the machine.

Whatever the reason, the two colleges having two dialysis machines each are not doing dialysis for one and half to two years. Recently the medicine department of GMCH, which had posted its resident doctors at SSH, has withdrawn them. Hence SSH, which has five dialysis machines, is able to manage just 10 patients a day. "We need five more machines considering the patient load. We have written to the directorate of medical education and research (DMER) for posting residents to at least continue the existing process," said the SSH Officer on Special Duty Dr Manish Shirigiriwar.

The machine operators and nursing staff have to work in shifts and in night when senior teachers are not there, resident doctors are needed to supervise the process. After the withdrawal of residents, the hospital had to stop taking patients in emergency in the night. DMER director Dr Pravin Shingare told TOI he would inquire with the GMC dean on why he had withdrawn the residents. "There must be some reason for him to do so. I will ask him before taking any decision of appointing new residents," he said.

The GMC medicine department has taken back the house officer who would work in night. "It is a life-saving procedure. What should the patient do? He is not aware of internal problems of the hospital. What reply should the hospital give the patients coming in emergency," asked a senior teacher.

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