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Damen delivers new Fast ferry series vessel to South Koreas Seaworld Express

2015-10-06 09:30:00| Ship Technology

Damen Shipyards has delivered a new high-speed catamaran passenger ferry, the Queen Star 2, to Seaworld Express Ferry.

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Heartland Express Stock Rating Reaffirmed by Barclays

2015-10-05 22:08:36| Trucking - Topix.net

's stock had its "sell" rating reaffirmed by equities research analysts at Barclays in a research report issued to clients and investors on Monday, MarketBeat Ratings reports. Shares of Heartland Express traded up 0.44% during trading on Monday, reaching $20.63.

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TNT Express Says Third-Quarter Profit Fell on Brazil, China Woes

2015-10-05 15:41:15| Trucking - Topix.net

TNT Express NV, the Dutch logistics company being taken over by FedEx Corp., said third-quarter profit fell because of economic turmoil in markets such as Brazil, China and Australia. Adjusted operating income in the period was probably "materially lower" than last year, TNT said in a statement prior to an extraordinary shareholder meeting at its headquarters in Hoofddorp on Monday.

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TNT Express Says Third-Quarter Profit Fell on Brazil, China Woes

2015-10-05 11:30:46| Air Courier - Topix.net

TNT Express NV, the Dutch logistics company being taken over by FedEx Corp., said third-quarter profit fell because of economic turmoil in markets such as Brazil, China and Australia. Adjusted operating income in the period was probably "materially lower" than last year, TNT said in a statement prior to an extraordinary shareholder meeting at its headquarters in Hoofddorp on Monday.

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FDA Approves KEYTRUDA (pembrolizumab) for the Treatment of Patients with Metastatic Non-Small Cell Lung Cancer Whose Tumors Express PD-L1 with Disease Progression On or After Platinum-Containing Chemotherapy

2015-10-02 20:49:00| Merck.com - Product News

Dateline City: KENILWORTH, N.J. Patients with EGFR or ALK Genomic Tumor Aberrations Should Have Disease Progression on FDA-Approved Therapy for These Aberrations Prior to Receiving KEYTRUDA KENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside the United States and Canada, today announced that the U.S. Food and Drug Administration (FDA) has approved KEYTRUDA (pembrolizumab) monotherapy, the companys anti-PD-1 (programmed death receptor-1) therapy, at a dose of 2 mg/kg every three weeks, for the treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors express PD-L1 as determined by an FDA-approved test and who have disease progression on or after platinum-containing chemotherapy. Language: English Contact: MerckMedia Contacts:Pamela Eisele, 267-305-3558Courtney Ronaldo, 908-236-1108orInvestor Contacts:Teri Loxam, 908-740-1986Justin Holko, 908-740-1879 Ticker Slug: Ticker: MRK Exchange: NYSE read more

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