Study Shows Neuralstem Cells Transplanted Into Brain Significantly Improve Post-Stroke Symptoms in Rats

First Study To Validate Cell Survival and Functionality in Brain, Improvement Dose Dependent

Neuralstem, Inc. (NYSE MKT: CUR) announced that a study published in the peer-reviewed journal, PLOS ONE, showed that ischemic-stroke rats transplanted with Neuralstem's NSI-566 stem cells in the brain experienced functional improvements. Furthermore, the grafts both survived and differentiated into neurons. These findings further validate the application of the cells for transplantation therapy in ischemic stroke.  The researchers concluded that the NSI-566 cells are potent cell donors for transplantation therapy to treat paralysis in stroke patients

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Idera Pharmaceuticals Announces Positive Top-line Data in Phase 2 Trial of IMO-8400

Trial meets primary objective of demonstrating safety and tolerability over 12-week treatment period
IMO-8400 also demonstrates clinical proof-of-concept in psoriasis

Idera Pharmaceuticals, Inc. (IDRA) today announced positive top-line data from its randomized, double-blind, placebo controlled Phase 2 trial of IMO-8400 in 32 patients with moderate-to-severe plaque psoriasis. The primary objective of the trial was to evaluate the safety and tolerability of IMO-8400 over a 12-week treatment period, with a secondary objective to evaluate the clinical activity of IMO-8400.

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Medicure Reports Financial Results for the Third Quarter Fiscal 2014

Medicure Inc. ("Medicure" or the "Company") (TSX VENTURE:MPH) (MCUJF), a specialty pharmaceutical company, today reported its results from operations for the quarter ended February 28, 2014.

Financial Results

Net revenue from the sale of AGGRASTAT finished product for the three months ended February 28, 2014 increased by 266% to $1.6 million from $447,000 for the three months ended February 28, 2013.

The increase in revenue for the three months ended February 28, 2014 compared to the same period in the prior year is primarily attributable to an increase in the number of new hospital customers using AGGRASTAT, which is driving an overall increase in hospital and wholesale demand.

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ProMetic Reports its 2013 Fourth Quarter and Financial Year End Results and Business Highlights

- PBI-4050 clinical program progressed with initiation in diabetic patients with chronic kidney disease expected in early H2 2014 - Plasminogen clinical pathway confirmed in a pre-IND meeting with the FDA - initiation in patients expected in early H2 2014 - Additional plasma-derived orphan drugs to be enabled in 2014 by the successful launch of the plasma facility - 2013 revenue of $20.6 million and EBITDA of ($8.7 million), Q4 2013 revenues of $5.1 million and EBITDA of ($3.8 million) - Balance sheet strengthened by financings

ProMetic Life Sciences Inc. (PLI.TO)(PFSCF) ("ProMetic" or the "Corporation") today reported revenues of $5.1 million and $20.6 million for the quarter and year ended December 31, 2013 respectively. This compares to revenues of $8.3 million and $23.3 million for the quarter and year ended December 31, 2012 respectively.

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Galectin Therapeutics to Announce Results From First Cohort of Phase 1 Clinical Trial in Fatty Liver Disease

Company to Hold Webcast and Conference Call on April 1 to Review Findings

Galectin Therapeutics (GALT), the leading developer of therapeutics that target galectin proteins to treat fibrosis and cancer, announced that on Monday, March 31, 2014, the Company will report results from the first cohort of its Phase 1 clinical trial examining GR-MD-02 in fatty liver disease (NASH) with advanced fibrosis. The first-in-man study, which enrolled eight patients in the first cohort, is evaluating the safety, tolerability, and exploratory biomarkers for efficacy for single and multiple doses of galectin inhibiting drug GR-MD-02 when administered to patients with fatty liver disease with advanced fibrosis.

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