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Tiziana Life Sciences
Tiziana Life Sciences was incorporated by serial biotech entrepreneur Gabriele Cerrone in 1998, initially operating on the London Stock Exchange before...
Tiziana Life Sciences
Tiziana Life Sciences was incorporated by serial biotech entrepreneur Gabriele Cerrone in 1998, initially operating on the London Stock Exchange before migrating its listing to the Nasdaq in November 2020. Cerrone, who also co-founded Cardiff Oncology and chaired Hepion Pharmaceuticals, has a history of structuring public biotech vehicles that target narrow, high-risk clinical pipelines. The firm operated as a publicly traded company for over two decades until February 2023, when Cerrone took it private through a merger with a subsidiary of Plan B Merger Sub, Inc., valued at approximately $1.20 per share in a cash transaction that closed in early 2024. The move removed the company from the public reporting environment. The firm deploys capital exclusively into the clinical development of its proprietary intranasal foralumab program, a fully human anti-CD3 monoclonal antibody. Tiziana holds a patent portfolio covering intranasal and oral delivery of anti-CD3 molecules. The primary indication is non-active secondary progressive multiple sclerosis, where an FDA-allowed expanded access program has reported improved clinical outcomes in a small patient cohort. Additional exploratory programs target Alzheimer's disease and long COVID patients with neuroinflammation. The firm does not maintain a diversified asset-class allocation and has no fund commitments or co-investment structures typical of a traditional asset manager — it operates more like a single-product, internally funded biotech platform. Existing clinical sites are concentrated in the United States, with neuroimaging and immunology collaborations at Harvard-affiliated laboratories and larger neurodegenerative research centers. Tiziana operates with a small executive team, led by Cerrone as Executive Chairman from his New York base and Matthew Davis, an MD with prior roles at Biogen and Allergan, as Chief Medical Officer. The firm maintains additional administrative operations in the UK and Bermuda. It does not run a venture arm, a foundation, or a multi-family wealth platform. March 2024: Tiziana published positive six-month interim data from its expanded access program in a peer-reviewed journal, reporting stable or improved clinical scores across a majority of the 10 enrolled patients. In August 2024, the firm presented new neuroimaging biomarker data showing reductions in microglial activation measured by PET scans (per the firm's press release, August 2024). These data points support an Investigational New Drug application for a pivotal trial — a binary clinical milestone that will define the next phase of the firm's existence. Tiziana's structural differentiator lies in its drug-delivery mechanism rather than its corporate form. Intranasal anti-CD3 treatment bypasses the blood-brain barrier through the olfactory nerve, a route that differentiates it from systemic monoclonal antibody approaches used by larger neurology players. The firm's decision to go private in 2024 also isolates it from equity-market scrutiny typical of early-stage public biotechs, giving Cerrone full discretion over clinical timelines and financing decisions — but also leaving external allocators with no transparency into its capitalization or cash runway.
General information
Firm type
Asset Manager
Year founded
1998
AUM
Undisclosed
Location
Region
Europe
Country
United Kingdom
City
London
Corporate office
London, United Kingdom
Additional offices
New York, NY, United States
Principals
Gabriele Cerrone
Executive Chairman and interim Chief Executive Officer
Matthew W. Davis
Chief Medical Officer
Sector focus
Frequently asked questions
Who runs investment decisions at Tiziana Life Sciences?
Gabriele Cerrone, the founder and Executive Chairman, makes all capital allocation decisions. Cerrone is a serial biotech entrepreneur who has chaired or co-founded multiple clinical-stage public companies including Cardiff Oncology. No separate investment committee or external advisor is disclosed by the firm.
What is Tiziana's lead clinical asset, and what is its mechanism of action?
The lead asset is intranasal foralumab, a fully human anti-CD3 monoclonal antibody. The drug modulates immune cell activity by binding to the CD3 receptor on T cells, and its intranasal route of administration is designed to bypass the blood-brain barrier and exert an anti-inflammatory effect directly on the central nervous system. This mechanism targets neuroinflammation, which the firm argues is a central driver in multiple sclerosis, Alzheimer's, and long COVID.
Is Tiziana a family office, an asset manager, or a biotech company?
Tiziana Life Sciences operates as a clinical-stage biotechnology platform, not as a diversified asset manager or a family office. It is controlled by founder Gabriele Cerrone and deploys all capital toward its in-house drug development programs. Following its February 2024 going-private transaction from the Nasdaq, the firm has no public equity or multi-asset investment mandate.
What is the status of Tiziana's multiple sclerosis program?
As of late 2024, foralumab is in an FDA-allowed expanded access program for non-active secondary progressive multiple sclerosis. Interim data described stable or improved clinical outcomes in a majority of the 10 treated patients. The firm has submitted an Investigational New Drug application to move into a formal Phase 2 pivotal trial, the regulatory outcome of which is the key binary event for the firm.
Does Tiziana raise outside capital or maintain fund commitments?
Tiziana does not operate as a fund manager and has not historically taken third-party limited partner capital. Prior to going private in February 2024, it was an equity-financed public company. Its current financing structure since the take-private is not publicly disclosed, and there are no known institutional fund commitments or co-investment vehicles open to external allocators.
How does Tiziana differ from larger neurology-focused biotech firms?
The primary differentiation is its intranasal anti-CD3 delivery route, which avoids the systemic immunosuppression and blood-brain barrier penetration challenges of intravenous monoclonal antibodies. Competitively, the firm is focused on a neuroinflammatory mechanism distinct from the B-cell depletion or myelin-repair approaches pursued by larger players like Roche and Biogen, though Tiziana operates at a vastly smaller scale.
What regulatory milestones should an allocator or partner track?
The near-term catalyst is the FDA's clearance of an Investigational New Drug application for a pivotal Phase 2 trial in secondary progressive multiple sclerosis. Additional data readouts from the expanded access program and the long COVID pilot study are expected to be submitted for publication. Any partnership or licensing announcement for foralumab would also be a material indicator of third-party validation.
Profile maintained by Altss using OSINT (open-source intelligence), regulatory filings, licensed data partners, and verified direct submissions. Read the methodology. Last updated: . Continuous refresh with full update cycles at least every 30 days.
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