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OBI Pharma confirms FDA’s clearance of IND for Phase 1 Study of Monoclonal Antibody Cancer…
U.S FDA clears OBI Pharma's investigational new drug (IND) application for a Phase 1 study of a monoclonal antibody cancer immunotherapy targeting Globo H, a glycolipid antigen…
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BioLineRx declares partial results for BL-8040’s Phase 2a COMBAT study
BioLineRx, committed to oncology and immunology declared partial results from the monotherapy portion of BL-8040's Phase 2a COMBAT study. The study reveals that BL-8040 increases…
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MiMedx enrolls first patients in the Phase 3 IND Clinical Trial for treating Achilles Tendonitis
MiMedx Group confirmed the enrollment of first patients in the Company's Phase 3 Investigational New Drug (IND) Clinical Trial for MiMedx's micronized amniotic tissue, AmnioFix…
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GC Pharma conducts Phase 2/3 Clinical Trial for GC1102 forbidding hepatitis B virus
GC Pharma, a South Korean biopharmaceutical company affirmed that it will conduct Phase 2/3 clinical trial for GC1102, the company's investigational recombinant hepatitis B immune…
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FDA Commissioner Scott Gottlieb,M.D., vows to enhance clarity of Clinical Trial information
In a bid to ensure transparency and clarity in their drug approval decisions, U.S FDA Commissioner Scott Gottlieb endeavors to undertake new drug innovation and Scientific progress by…
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Nils Hauptmann appointed Aerie Pharma’s Director of Regulatory Affairs and Pharmacovigilance
Ophthalmic Pharmaceutical Company, Aerie Pharmaceuticals that seeks to treat patients with open-angle glaucoma and other diseases of the eye declared the appointment of Nils Hauptmann…
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Ophthotech enlists first patient for Phase 2b Clinical Trial of Zimura to treat STGD1
Ophthotech Corporation enrolled first patient in the Phase 2b randomized, double-masked, sham-controlled clinical trial assessing the efficacy and safety of Zimura complement C5…
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FDA issues 510(k) clearance to Centric Medical for Cannulated Screw Internal Fixation System
Developer of surgical implants for treating distal extremity pathology, Centric Medical asserted that the U.S FDA has granted 510 (k) clearance to the Cannulated Screw Internal Fixation…
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START collaborates with Sarah Cannon to accelerate Phase I drug development programs
Sarah Cannon Research Institute and South Texas Research Accelerated Therapeutics moved to collaborate ensuring augmenting their globally acclaimed phase I drug development programs…
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Ipsen and Exelixis proclaims phase 3 CELESTIAL Trial results in patients with HCC
Ipsen and Exelixis declared results of Phase 3 CELESTIAL trial in patients formerly treated with advanced heptacellular carcinoma. In CELESTIAL, cabozantinib provided a statistically…
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AvantGen completes first Cancer therapeutic antibody program for TRL
Antibody discovery and optimization service provider, AvantGen claimed completion of its first cancer therapeutic antibody program in collaboration with Tanabe Research Laboratories USA…
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Edwin Miranda entitled VP of Cytovance’s Quality Biologics
Cytovance Biologics a biopharmaceutical contract manufacturer of mammalian and microbial biologics proclaimed Edwin Miranda as Vice-President of Quality.
Dr. Jesse McCool, Sr. Vice…
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Lustgarten Foundation claimed $22 million funding for Pancreatic Cancer research
Lustgarten Foundation alleges $22 million funding in 2017 as part of its mission to invest an unprecedented $40 million by the end of 2018. In a bid to advanced pancreatic Cancer…
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Raymond Kaczmarek appointed President by Nitto Avecia Pharma
CGMP contract development and manufacturing organization (CDMO), Nitto Avecia Pharma Services appointed Raymond Kaczmarek as the president entrusting the P&L responsibility for the…
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Diplomat Pharmacy offers CABOMETYX treatment for RCC
Diplomat Pharmacy mets out CABOMETYX treatment for Renal cell carcinoma inflicted on patients as approved by the Food and Drug administration. Formerly approved as a second-line therapy…
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BD and Check-Points attains CE Mark for next-generation molecular screening test
BD (Becton, Dickinson and Company), global medical technology company, along with Check-Points Health B.V., affirmed that the companies sought CE Mark for a next-generation molecular…
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Bio-Techne offers reagents and kits from Vector Laboratories
Labeling and detection solutions, Bio-Techne now provides reagents and kits from Vector Laboratories that doles out reliable, sensitive, and low background detection. In October, 2017,…
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Dawn Barry declared President of Luna DNA
Genomic and Medical research knowledge base powered by the blockchain and owned by its community, Luna DNA declared Dawn Barry as president. Barry will be held accountable for leading…
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USRM alleges 10,000 kit sales of Adipocell product
U.S Stem Cell, Inc. claimed to be a leader in the development of proprietary stem cell therapies asserted accomplishing the target of 10,000 kit sales of proprietary Adipocell product,…
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FDA sanctions Teva Pharmaceutical’s TRISENOX for Acute Promyelocytic Leukemia treatment
U.S FDA approves Teva Pharmaceutical's TRISENOX i.e. Arsenic trioxide injection amalgamated with tretinoin in the therapy of adults diagnosed with low -risk acute promyelocytic…
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