Last $1.81 USD
Change Today -0.04 / -2.16%
Volume 41.0K
CRMD On Other Exchanges
Symbol
Exchange
NYSE Amex
As of 8:04 PM 10/24/14 All times are local (Market data is delayed by at least 15 minutes).

cormedix inc (CRMD) Snapshot

Open
$1.82
Previous Close
$1.85
Day High
$1.84
Day Low
$1.74
52 Week High
03/3/14 - $3.20
52 Week Low
11/20/13 - $0.66
Market Cap
39.8M
Average Volume 10 Days
37.4K
EPS TTM
$-1.00
Shares Outstanding
22.0M
EX-Date
--
P/E TM
--
Dividend
--
Dividend Yield
--
Current Stock Chart for CORMEDIX INC (CRMD)

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cormedix inc (CRMD) Details

CorMedix Inc., a development-stage pharmaceutical and medical device company, intends to in-license, develop, and commercialize therapeutic products for the treatment of cardiorenal and infectious diseases. The company’s product candidates include CRMD003 (Neutrolin) and CRMD004, an antimicrobial/antifungal and anticoagulant combination in liquid and gel formulations used for the prevention of catheter-related blood stream infections and maintenance of catheter patency in hemodialysis patients. The company was formerly known as Picton Holding Company, Inc. and changed its name to CorMedix Inc. in January 2007. CorMedix Inc. was founded in 2006 and is based in Bridgewater, New Jersey.

2 Employees
Last Reported Date: 03/31/14
Founded in 2006

cormedix inc (CRMD) Top Compensated Officers

Chief Executive Officer and Director
Total Annual Compensation: $223.5K
Vice Chairman, Chief Scientific Officer and C...
Total Annual Compensation: $120.0K
Compensation as of Fiscal Year 2013.

cormedix inc (CRMD) Key Developments

CorMedix Inc. Announces FDA IND Filing for Neutrolin(R) in United States

CorMedix Inc. announced that an Investigational New Drug application (IND) for Neutrolin(R) was submitted to the United States Food and Drug Administration (FDA) on September 24, 2014. The IND includes a pivotal Phase 3 protocol for Neutrolin(R) in hemodialysis patients with a central venous catheter. The Phase 3 clinical trial is designed as a multi-center, randomized, controlled study conducted in the U.S. and Europe. Dr. Michael Allon, Professor, Department of Medicine, Division of Nephrology, University of Alabama, Birmingham will be the Study Chair of the Neutrolin(R) Phase 3 program. An IND goes into effect 30 days after FDA receives the IND, unless FDA provides notification that the IND is subject to a clinical hold.

CorMedix, Inc. to Report Q2, 2014 Results on Aug 14, 2014

CorMedix, Inc. announced that they will report Q2, 2014 results on Aug 14, 2014

U.S. Food and Drug Administration Accepts CorMedix , Inc.'s Pivotal Phase 3 Study Protocol

CorMedix Inc. announced that U.S. Food and Drug Administration (FDA) has agreed with the design of pivotal Phase III protocol for Neutrolin(R) in Hemodialysis patients, and the company plans to submit the IND for Neutrolin within the next 30 days. The FDA will then have 30 days to respond to the IND. The pivotal Phase 3 randomized controlled trial for Neutrolin is for use in hemodialysis patients with a central venous catheter. The Phase 3 clinical trial will be a multi-center, randomized, controlled study conducted in the U.S. and Europe. Dr. Michael Allon, Professor, Department of Medicine, Division of Nephrology, University of Alabama, Birmingham will be the Study Chair of the Neutrolin Phase 3 program.

 

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