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BioSpace News Archive
Browse BioSpace’s published news and press releases by year, month, and day.
70 Results
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Business
AbSci Appoints Fred Larimore, PhD to Scientific Advisory Board
Prior to formally joining AbSci’s Scientific Advisory Board, Dr. Larimore advised AbSci on various aspects of biopharmaceutical process development manufacturing scale-up.
December 22, 2017
·
2 min read
Business
MediSapiens Joins the FinnGen Project and Brings Solutions to Curation, Management and Visualization of Genetic and Clinical Data of 500.000 Finns
MediSapiens will provide its data curation, data management, data exploration and discovery software solutions to FinnGen, and will be an active technology partner in the project.
December 22, 2017
·
4 min read
Business
West Pharma Services Announces Quarterly Dividend and Participation in Upcoming Investor Conferences
West Pharmaceutical Services today announced that the Company’s Board of Directors has approved a first-quarter 2018 dividend of $0.14 per share.
December 22, 2017
·
1 min read
Business
NovaBay Pharmaceuticals Receives Stockholder Approval for Proposed $10.32 Million Financing Agreement
NovaBay announces stockholder approval to issue NovaBay common stock as part of a $10.32 million financing agreement with Ch-gemstone Capital (Beijing) Co., Ltd.
December 22, 2017
·
3 min read
FDA
Merck Release: FDA Approves SGLT2 Inhibitor STEGLATRO™ (ertugliflozin) and Fixed-Dose Combination STEGLUJAN (ertugliflozin and sitagliptin) for Adults With Type 2 Diabetes
STEGLATRO is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
December 22, 2017
·
29 min read
Business
gel-e Expands Board of Directors With Domain & Commercial Strategy Expert
gel-e, a privately held, clinical-stage medical device company, announces the expansion of its Board of Directors to include industry veteran Jim Buck.
December 22, 2017
·
2 min read
Drug Development
Novartis’ Combination Therapy Tafinlar + Mekinist Granted FDA Priority Review for the Adjuvant Treatment of Stage III BRAF V600 Mutation-Positive Melanoma
Novartis announced today the FDA has accepted the Company’s supplemental sNDA for filing, and granted Priority Review designation for Tafinlar in combination with Mekinist for the adjuvant treatment of patients with stage III melanoma with BRAF V600E or V600K mutations, as detected by an FDA-approved test, following complete resection.
December 22, 2017
·
15 min read
Drug Development
Arrowhead Pharmaceuticals Files for Regulatory Clearance to Begin Phase I/II Study of ARO-HBV
Pending approval, Arrowhead intends to proceed with AROHBV1001, a Phase 1/2 single-dose escalation study to evaluate the safety, tolerability, and pharmacokinetic effects of ARO-HBV in healthy adult volunteers
December 22, 2017
·
3 min read
Paragon 28 Launches the Gorilla Lateral Column Plating System - the First Dedicated Plating System Designed to Address the Cuboid and Lateral Column in Cases of Charcot Deformity
Committed to creating tailored solutions to improve surgical outcomes, Paragon 28 has launched innovative products and instrumentation that help to streamline procedures, allow surgeons flexibility in technique and approach, and facilitate reproducible results benefitting both the surgeon and patient.
December 22, 2017
·
2 min read
Business
Lifestyle Delivery Systems’ Licensee, CSPA Group, Receives California State License Type 7 Manufacturing License for Volatile Solvent Extraction
During this time, the California Department of Public Health will review CSPA’s application and corresponding municipal permits and documentation for a permanent license.
December 22, 2017
·
3 min read
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