CRBP-300-196.png
Corbus Pharmaceuticals Initiates “DETERMINE” Phase 3 Study in Dermatomyositis
December 17, 2018 07:00 ET | Corbus Pharmaceuticals Holdings, Inc.
DM is a rare systemic autoimmune disease that affects ~80,000 individuals in the U.S., EU and Japan and has a 5-year mortality rate as high as 30% This marks Company’s second Phase 3 program in rare...
PAVMEDLOGONEW15OCT2018.png
PAVmed Provides Business Update
October 17, 2018 07:30 ET | PAVmed Inc.
NEW YORK, Oct. 17, 2018 (GLOBE NEWSWIRE) -- PAVmed Inc. (Nasdaq: PAVM, PAVMZ) (the “Company” or “PAVmed”), a highly differentiated, multiproduct medical device company, today provided an update on...
CRBP-300-196.png
Corbus Pharmaceuticals Receives Orphan Designation for Lenabasum for the Treatment of Dermatomyositis in the European Union
September 18, 2018 08:05 ET | Corbus Pharmaceuticals Holdings, Inc.
– Dermatomyositis is a rare chronic systemic autoimmune disease characterized by inflammation of muscles and skin – DM affects ~80,000 in the US, EU and Japan and has a 5-year mortality rate as...
respirerx.jpg
RespireRx Pharmaceuticals Inc. Secures Clinical and Commercial Supply of Dronabinol for Obstructive Sleep Apnea with the Signing of a Development and Supply Agreement with Noramco, Inc.
September 10, 2018 15:30 ET | RespireRX Pharmaceuticals Inc.
Glen Rock, N.J., Sept. 10, 2018 (GLOBE NEWSWIRE) -- September 10, 2018 /Globe Newswire – RespireRx Pharmaceuticals Inc. (OTCQB: RSPI) (“RespireRx” or the “Company”), is pleased to announce that on...
U.S. FDA Approves Te
U.S. FDA Approves Terumo BCT’s Sodium Citrate 4% w/v Anticoagulant Solution Amid Shortage
July 18, 2018 10:04 ET | Terumo BCT
Lakewood, Colorado, USA, July 18, 2018 (GLOBE NEWSWIRE) -- The U.S. Food and Drug Administration (FDA) recently approved Terumo BCT’s Sodium Citrate 4% w/v Anticoagulant Solution USP, indicated for...
Epilepsy Foundation
Epilepsy Foundation Testifies Before FDA Advisory Committee in Support of Potential First-Ever Cannabidiol Drug to Treat Dravet Syndrome
April 19, 2018 12:07 ET | Epilepsy Foundation
WASHINGTON, April 19, 2018 (GLOBE NEWSWIRE) -- Philip Gattone, president and CEO of the Epilepsy Foundation, along with other epilepsy advocates, today testified at the U.S. Food & Drug...
ABTLOGO.jpg
Advanced Biomedical Technologies Inc. Announces Chinese CFDA Approval of Polymer Fixation Screws
April 19, 2018 11:50 ET | Advanced Biomedical Technologies Inc
SHENZHEN, CHINA and NEW YORK, April 19, 2018 (GLOBE NEWSWIRE) -- Advanced Biomedical Technologies Inc. (OTCQB:ABMT), a developer and manufacturer of orthopaedic internal fixation devices, announced...
sintx_grn_blk@4x-8.png
Amedica announces FDA Clearance of the Valeo C+CSC with Lumen Interbody Fusion Device
March 06, 2018 09:00 ET | Amedica Corporation
SALT LAKE CITY, UT, March 06, 2018 (GLOBE NEWSWIRE) -- Amedica Corporation (NASDAQ: AMDA), an innovative biomaterial company that develops and commercializes silicon nitride as a platform for...
FDA to Send Contract
FDA to Send Contractor to Inspect Vape Shops
February 15, 2018 12:38 ET | US Federal Contractor Registration
Rockville, MD, Feb. 15, 2018 (GLOBE NEWSWIRE) -- The Food and Drug Administration (FDA) will be sending a contractor to inspect entities engaged in retail activities where tobacco regulated products...
Axim-Sapphire_Logo_-04 (1).png
AXIM Biotech Announces Successful Completion of Pre-IND Meeting with FDA on Comparable Product to Marinol; Green Light from FDA for IND Submission
December 12, 2017 09:00 ET | AXIM BIOTECHNOLOGIES, INC
NEW YORK, Dec. 12, 2017 (GLOBE NEWSWIRE) -- AXIM® Biotechnologies, Inc. (OTC:AXIM), a world leader in cannabinoid research and development, announced today that it has successfully completed a...