COMMUNIQUÉS West-GlobeNewswire

Quotient Limited Announces Initial MosaiQ™ SDS Verification and Validation Data
03/12/2018
JERSEY, Channel Islands, Dec. 03, 2018 (GLOBE NEWSWIRE) -- Quotient Limited (NASDAQ:QTNT), a commercial-stage diagnostics company (the Company), today reported positive Verification and Validation (V&V) concordance [...]
Nephros to Present at the 11th Annual LD Micro Main Event
03/12/2018
Presentation Scheduled for 9:30 AM PT on Tuesday, December 4th SOUTH ORANGE, NJ, Dec. 03, 2018 (GLOBE NEWSWIRE) -- via NEWMEDIAWIRE – Nephros, Inc. (OTCQB: NEPH) (“Nephros”), a commercial stage medical device company [...]
Onconova Highlights Results from Phase 2 Trial of Oral Rigosertib In Combination with Azacitidine (Vidaza®) in Myelodysplastic Syndromes (MDS) at the 2018 ASH Annual Meeting
03/12/2018
Overall response rate (ORR) of 90% reported in this multi-institutional Phase 2 study in hypomethylating agent (HMA) naïve patients, including Complete Remission (CR) rate of 34% ORR of 54% and CR/Partial Response (PR) [...]
Theratechnologies Appoints New Chief Commercial Officer
03/12/2018
MONTREAL, Dec. 03, 2018 (GLOBE NEWSWIRE) -- Theratechnologies Inc. (Theratechnologies) (TSX: TH) is pleased to announce the appointment of Mr. Jovan Antunovic as Senior Vice President and Chief Commercial Officer. “ [...]
Theratechnologies nomme un nouveau chef de l’exploitation commerciale
03/12/2018
MONTRÉAL, 03 déc. 2018 (GLOBE NEWSWIRE) -- Theratechnologies Inc. (Theratechnologies) (TSX: TH) est heureuse d’annoncer la nomination de M. Jovan Antunovic à titre de vice-président principal et chef de l’exploitation [...]
Xenon Announces Final Results of XEN1101 Phase 1 Clinical Trial and Update on XEN901 Phase 1 Clinical Trial at the American Epilepsy Society (AES) Annual Meeting
03/12/2018
XEN1101 CTA Accepted by Health Canada for Initiation of Phase 2 Clinical Trial in Adult Focal Epilepsy; U.S. IND Filing Targeted in Q1 2019 Conference Call to Discuss Xenon’s Epilepsy Programs at 9 am ET Today BURNABY, [...]
Cytori Announces Japan Class III Medical Device Approval for Cell Therapy Product
03/12/2018
Expands medical device production capabilities SAN DIEGO and TOKYO, Dec. 03, 2018 (GLOBE NEWSWIRE) -- Cytori Therapeutics (NASDAQ: CYTX) (“Cytori” or the “Company”) today announced that the Company has received approval [...]
Aptinyx Reports Positive Data from Interim Analysis of Exploratory Study of NYX-2925 in Subjects with Fibromyalgia
03/12/2018
Achieved statistical significance on primary imaging-based endpoint, changes in markers of central pain processing, in 11 subjects Observed corresponding trends of improvement on multiple secondary endpoints, including [...]
Bio-Path Holdings Presents Interim Data from Phase 2 Study Evaluating Prexigebersen as a Treatment for Acute Myeloid Leukemia at the 60th Annual American Society of Hematology Annual Meeting
03/12/2018
HOUSTON, Dec. 03, 2018 (GLOBE NEWSWIRE) -- Bio-Path Holdings, Inc., (NASDAQ: BPTH), a biotechnology company leveraging its proprietary DNAbilize ® antisense RNAi nanoparticle technology to develop a portfolio of [...]
OHSU and Aptose Present New CG-806 Preclinical Data at ASH 60th Annual Meeting
03/12/2018
CG-806 Pan-FLT3/Pan-BTK Inhibitor Exhibits Favorable Safety Profile and Unexpected Potency on Primary Cells from B-cell Cancer Patients and AML Patients PORTLAND, Ore. and SAN DIEGO, Dec. 03, 2018 (GLOBE NEWSWIRE) -- [...]
Aptose Presents New Preclinical Data on CG-806 PAN-FLT3/PAN-BTK Inhibitor at ASH 60th Annual Meeting
03/12/2018
Data elucidate unique ability of CG-806 to overcome resistance to other FLT3 inhibitors in AML cells SAN DIEGO and TORONTO, Dec. 03, 2018 (GLOBE NEWSWIRE) -- Aptose Biosciences Inc. (NASDAQ: APTO, TSX: APS) today [...]
Advanced Accelerator Applications signs exclusive option and license agreement with FUJIFILM Toyama Chemical to develop and commercialize radiolabeled FF-10158 for oncology indications
03/12/2018
Novel small molecule FF-10158 targets integrin alphavbeta3 ( a v β3 ) and alphavbeta5 ( a v β5 ) receptors Expands theragnostic pipeline Potential broad application in the detection and treatment of highly vascularized [...]
Genmab to Hold R&D Update and 2018 ASH Data Review Meeting
03/12/2018
Media Release Event to be held today in San Diego, California Independent experts to discuss data presented at the 2018 ASH Annual Meeting Meeting to be webcast live and archived on www.genmab.com Copenhagen, Denmark; [...]
GENFIT: Launch of a U.S. Phase 2 investigator-initiated study with nitazoxanide in patients with NASH-induced fibrosis
03/12/2018
GENFIT: Launch of a U.S. Phase 2 investigator-initiated study with nitazoxanide in patients with NASH-induced fibrosis Phase 2 study targeting a patient population with NASH-induced Stage 2 or 3 fibrosis Anti-fibrotic [...]
GENFIT : Lancement aux États-Unis d'une étude de Phase 2 initiée par un investigateur, évaluant nitazoxanide chez des patients avec fibrose NASH
03/12/2018
GENFIT : Lancement aux États-Unis d'une étude de Phase 2 initiée par un investigateur, évaluant nitazoxanide chez des patients avec fibrose NASH Étude de phase 2 ciblant une population de patients atteints de NASH avec [...]
Press release: Terveystalo to become a shareholder in startup company Etsimo Healthcare - harnessing AI to assist the customer and the healthcare professional
03/12/2018
Terveystalo has signed a contract on 27 November to acquire a share of about 20% in Etsimo Healthcare Oy. Etsimo Healthcare was established in 2016 and develops a platform built specifically for healthcare, combining [...]
Rule 2.9 Announcement
03/12/2018
NOT FOR RELEASE, PUBLICATION OR DISTRIBUTION IN WHOLE OR IN PART IN, INTO OR FROM ANY JURISDICTION WHERE TO DO SO WOULD CONSTITUTE A VIOLATION OF THE RELEVANT LAWS OR REGULATIONS OF THAT JURISDICTION. 3 December 2018 [...]
Total voting rights
03/12/2018
Total Voting Rights December 3, 2018 - Shire plc (LSE: SHP, NASDAQ: SHPG) (the “Company”), in accordance with 5.6.1R of the Financial Conduct Authority's (the “FCA”) Disclosure Guidance and Transparency Rules, notifies [...]
Novartis announces FDA filing acceptance and Priority Review of AVXS-101, a one-time treatment designed to address the genetic root cause of SMA Type 1
03/12/2018
The AVXS-101, now known as ZOLGENSMA ® (onasemnogene abeparvovec-xxxx)[1], filing is supported by data from the START trial which demonstrated a dramatic increase in survival and transformative improvement in [...]

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