INmune Bio Inc

INmune Bio Inc (INMB) News & Events

$2.330

-0.068 (-2.92%)At close

INMB News

INMB Events

8/26 07:30

INmune Bio Submits Ebstrocel Drug Applications

INmune Bio announced that it has submitted two regulatory packages to the European Medicines Agency, or EMA, for Ebstrocel: an application for orphan drug designation and a scientific advice package to streamline the upcoming marketing authorization application, or MAA, in Europe. Ebstroce is an investigational pooled, allogeneic, umbilical cord-derived mesenchymal stromal cell therapy being developed as a systemic treatment for recessive dystrophic epidermolysis bullosa. The EMA filings are intended to support the company's planned EU MAA in Q1 2027 and form part of a coordinated global registration strategy that includes a planned UK MAA in Q4 2026 and a planned U.S. biologics license application in Q1 2027.

7/20 07:30

INmune Bio Successfully Processes First Commercial-Ready Umbilical Cord Tissue

INmune Bio announced the company has successfully processed its first commercial-ready umbilical cord tissue at the Cell and Gene Therapy Catapult Manufacturing Innovation Centre in Stevenage, UK, under its commercial agreement with Anthony Nolan Cord Blood Bank. This achievement marks the transfer of the mesenchymal stromal cell isolation stage for the manufacture of master cell banks into INmune Bio's commercial manufacturing facility. The process is now commercial-ready to MHRA, EMA and FDA standards, including maternal blood samples infectious disease testing in US-CLIA-accredited laboratories. The technology transfer positions the company to generate its first U.S. tested master cell banks for Ebstrocel, the RDEB-specific investigational product derived from the CORDStrom platform, in support of its planned Phase 3 confirmation clinical trial and future commercial supply.

6/25 07:30

INmune Bio Receives Pediatric Investigation Plan Approval for Ebstrocel

INmune Bio announced that the UK Medicines & Healthcare products Regulatory Agency, or MHRA, has approved the pediatric investigation plan, or PIP, for Ebstrocel for the treatment of Recessive Dystrophic Epidermolysis Bullosa, or RDEB. The approval of the PIP is the first required stage toward a marketing authorization application, or MAA, submission in the United Kingdom. This regulatory milestone remains aligned with the company's established timetable for an MAA filing in 2026 and a US filing for Accelerated Approval in early 2027.

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