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Overview
The Company At Genespire, we develop off-the-shelf gene therapies. Our proprietary immune shielded lentiviral vectors (ISLV) are designed to allow life-long production of a therapy directly from a patient's liver, offering a one-time treatment for adults and children with genetic diseases.
News
Genespire and SR-TIGET Show Durable Preclinical Efficacy of Liver-Directed Gene Therapy for Methylmalonic Acidemia
Genespire, in collaboration with researchers at the San Raffaele Telethon Institute for Gene Therapy (SR-TIGET), has today announced the publication of preclinical data supporting the potential of its liver-directed immune-shielded lentiviral gene therapy
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Genespire and SR-TIGET Show Durable Preclinical Efficacy of Liver-Directed Gene Therapy for Methylmalonic Acidemia
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Genespire and SR-TIGET Show Durable Preclinical Efficacy of Liver-Directed Gene Therapy for Methylmalonic Acidemia
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Genespire announces oral presentation at the ASGCT Annual Meeting detailing preclinical insights into dosing for first-in-humanin vivo liver-directed ISLV gene therapy for MMA
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Genespire raises €46.6 million ($52 million) in a Series B round to advance its first pediatric in-vivo gene therapy into the clinic
Genespire raises €46.6 million ($52 million) in a Series B round to advance its first pediatric in-vivo gene therapy into the clinic One of the largest private Italian Biotech company financings to date Financing co-led by Sofinnova Partners, XGEN Venture
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Offices
Where the company hires and what each office is for
Cities
1
Hiring now
0
Countries
1
Milan
Italy
Registered seat
Legal address
Via Borgogna 5, 20122 Milano – Italy
Financials
Total raised
$50.3M
Latest round
Series B
Funding rounds
1
Funding rounds
| Round | Announced | Amount | |
|---|---|---|---|
| Series B | 2024 | $50.3M | Details |
