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CANbridge Pharmaceuticals Spinal Muscular Atrophy Gene Therapy Abstract Accepted for Presentation at the American Society for Gene and Cell Therapy annual Meeting

CANbridge Pharmaceuticals, Inc. announced that the American Society for Gene and Cell Therapy has accepted the following abstract for presentation at the ASCGT Annual Meeting, May 16-20, in Los Angeles, CA.

CANbridge Pharmaceuticals Spinal Muscular Atrophy Gene Therapy Abstract Accepted for Presentation at the American Society for Gene and Cell Therapy annual Meeting Read More »

Initiation of New Patients on Evobrutinib Paused in the U.S.; Fully Enrolled Phase III Evobrutinib Studies Continue

Merck KGaA, Darmstadt, Germany, a leading science and technology company, announced the U.S. Food and Drug Administration has placed a partial clinical hold on the initiation of new patients on evobrutinib and patients with less than 70 days exposure to study medication in the U.S.

Initiation of New Patients on Evobrutinib Paused in the U.S.; Fully Enrolled Phase III Evobrutinib Studies Continue Read More »

HUTCHMED Highlights Presentations at American Association for Cancer Research Annual Meeting 2023

HUTCHMED Limited announces that new and updated clinical and non-clinical data related to five HUTCHMED investigational drug candidates will be presented during the American Association for Cancer Research Annual Meeting 2023, which will take place from April 14 to 19, 2023 in Orlando, Florida.

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CHITOSE Group Obtains Funding from Japanese Government-affiliated NEDO for Green Innovation Fund of USD400M Range

Chitose Laboratory Corp. has won funding from a Japanese government-affiliated entity for a project on the self-proposed theme of “Building a global industry originating in Japan based on the direct use of CO2 through photosynthesis” for the “Green Innovation Fund Project : Promotion of Carbon Recycling Using CO2 from Biomanufacturing Technology as a Direct Raw

CHITOSE Group Obtains Funding from Japanese Government-affiliated NEDO for Green Innovation Fund of USD400M Range Read More »

ImaginAb Executes New License and Supply Agreement for CD8 ImmunoPET Technology with Leucid Bio

ImaginAb Inc. is pleased to announce the execution of a new non-exclusive License and Supply Agreement with Leucid Bio, a biotech company pursuing a differentiated approach to develop next generation Chimeric Antigen Receptor T-cell therapies using the Company’s proprietary Lateral CAR Platform.

ImaginAb Executes New License and Supply Agreement for CD8 ImmunoPET Technology with Leucid Bio Read More »

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