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Projects

Estimated Cost :
$14 Million
Cascade Chemistry Plans for Expansion of cGMP Pharmaceutical Manufacturing Capacity
Cascade Chemistry invests $14 million for construction of new facilities designed to increase

Estimated Cost :
-
Bristol Myers Squibb to invest in New Cell Therapy Manufacturing facility in Massachusetts, USA
Construction is underway for a new cell therapy manufacturing facility in Devens, Mass., a part of Bristol Myers Squibb’s

Estimated Cost :
-
Marker Therapeutics Plans to Construct New Manufacturing Facility in Texas
Marker Therapeutics plans to construct a new manufacturing facility to support clinical development of MultiTAA-Specific T cell therapy

Estimated Cost :
US$715 million
Merck Invests US$715 million in New Facility at Madison,USA
Merck with an investment of US$715 million plans for the expansion of Antibody-drug Conjugates (ADC) manufacturing. The new manufacturing facility wil...
Press Release
Lee’s Pharmaceutical Announces its Anti-PD-L1 Antibody Socazolimab, Licensed From Sorrento Therapeutics, Receives Clearance to Start Phase 3 Trial as a First-line Treatment
China Oncology Focus Limited (COF), an affiliate of Lee's Pharmaceutical Holdings Limited (Lee's Pharm, HKEX: 950) announced that its anti-PD-L1 antibody, Socazolimab, licensed from Sorrento to COF for the greater China territory, has been cleared to begin a multicenter
Hyloris’ Partner AFT Pharmaceuticals Signs Licensing Agreement with Aguettant for Maxigesic® IV in Eight European Markets
Hyloris Pharmaceuticals SA, a specialty biopharma company committed to bringing innovative treatments that offer added value to underserved patient populations, announces that its partner AFT Pharmaceuticals (“AFT”) has signed an exclusive licensing agreement with Aguettant for Maxigesic IV
Foresee Pharmaceuticals Enters Exclusive License Agreement with Intas Pharmaceuticals for Commercialization in the United States
Foresee Pharmaceuticals announced that it has entered into an exclusive license agreement with Intas Pharmaceuticals ("Intas") for the US commercialization of Foresee's novel FP-001 program, Leuprolide Mesylate Injectable Suspension (LMIS) ready-to-use subcutaneous 6-month and 3-month depot formulations
Luminex Receives FDA Emergency Use Authorization and CE Mark for Expanded NxTAG® Respiratory Panel Test Including SARS-CoV-2
Luminex Corporation announced that it has received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for a new expanded version of its NxTAG® Respiratory Pathogen Panel (RPP) that includes the SARS-CoV-2 virus for high-throughput respiratory testing.
Events

8th World Congress and Exhibition on Antibiotics and Antibiotic Resistance



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