FDA
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Celularity receives FDA warning letter over Interfyl marketing claims
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Celularity (CELU) Provides Corporate Update
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Celularity (CELU) Receives FDA Preliminary Assessment For Celularity’s Investigational Fuse Bone Void Filler To Be Regulated As A Device By FDA’s Center For Devices And Radiological Health
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Celularity CEO Robert J. Hariri, M.D., Ph.D., Addresses FII Conference on “The Science and Technology for Extending Healthy Human Lifespan”
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Celularity Announces Treatment of First Patient in Phase 1/2a Clinical Trial for NK Cell Therapy CYNK-101, in Development for the First-Line Treatment of Advanced HER2 Positive Gastric and Gastroesoph
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Celularity (CELU) Stock Gains 6% on FDA Fast Track Endorsement for CYNK-001
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Celularity Closes Merger with GX Acquisition Corp and Provides Corporate Update
323,712 total articles have been posted to this entity.
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