SciTransfer
Organization

PLURI BIOTECH LTD

Israeli biotech SME developing placenta-derived cell therapies (PLX-PAD) for muscle regeneration and orthopaedic recovery, with Phase III clinical data.

Technology SMEhealthILSMENo active H2020 projects
H2020 projects
4
As coordinator
0
Total EC funding
€6.1M
Unique partners
39
What they do

Their core work

Pluri Biotech (formerly Pluristem Therapeutics) is an Israeli biotech SME that develops placenta-derived cell therapies for regenerative medicine. Their core product, PLX-PAD — allogeneic placenta-derived stromal cells expanded ex vivo — targets muscle regeneration and recovery after orthopaedic trauma, particularly hip fractures. Within EU consortia, they contribute both the therapeutic product itself and the clinical-stage expertise needed to bring advanced therapy medicinal products (ATMPs) through Phase II/III trials.

Core expertise

What they specialise in

Placenta-derived cell therapy (PLX-PAD)primary
3 projects

Central to PACE (Phase IIb), HIPGEN (Phase III), and RESTORE, all focused on their proprietary PLX-PAD stromal cell product.

Orthopaedic regenerative medicineprimary
2 projects

PACE and HIPGEN both target muscle regeneration and recovery after hip fracture surgery.

Advanced therapy clinical trialssecondary
2 projects

PACE ran a multicenter Phase IIb and HIPGEN progressed to Phase III, demonstrating deep regulatory and clinical trial expertise.

Stem cell tracking and nanoparticle imagingsecondary
1 project

nTRACK project developed multimodal core-shell nanoparticles for structural and functional tracking of stem cell therapy on muscle regeneration.

Evolution & trajectory

How they've shifted over time

Early focus
Stem cell research and tracking
Recent focus
Phase III clinical translation

In their earlier H2020 involvement (2017), Pluri engaged in both upstream research — nanoparticle-based tracking of stem cell therapies (nTRACK) — and mid-stage clinical work (PACE Phase IIb). By 2018-2019, the focus shifted decisively toward late-stage clinical translation, with HIPGEN running a Phase III trial for hip fracture recovery and RESTORE connecting them to the broader ATMP community. The trajectory is clear: from research tools and early clinical validation toward regulatory-grade clinical evidence for their lead product.

Pluri is moving toward market-ready clinical evidence for PLX-PAD in orthopaedic indications, suggesting future collaborations will center on commercialization, regulatory approval, and expanded clinical applications.

Collaboration profile

How they like to work

Role: specialist_contributorReach: European16 countries collaborated

Pluri has participated exclusively as a consortium partner across all four projects, never as coordinator — consistent with an SME that brings a proprietary therapeutic product into larger research frameworks led by academic or clinical partners. With 39 unique partners across 16 countries, they integrate readily into large European consortia. Their role is that of a specialized contributor providing the cell therapy product and associated know-how, rather than managing the overall project.

Pluri has collaborated with 39 distinct partners across 16 countries, indicating a broad European network despite being based in Israel. Their consortia span clinical centers, universities, and nanotech labs, reflecting the multidisciplinary nature of advanced therapy development.

Why partner with them

What sets them apart

Pluri is one of very few SMEs globally with a proprietary, off-the-shelf (allogeneic) placenta-derived cell therapy platform at Phase III clinical readiness. Unlike autologous cell therapies that require patient-specific manufacturing, PLX-PAD cells can be produced at scale from donated placentas and used without HLA matching. For consortium builders, they offer a rare combination: an industry partner with both a manufacturable ATMP product and the clinical data to back it up.

Notable projects

Highlights from their portfolio

  • HIPGEN
    Phase III clinical study for hip fracture recovery using PLX-PAD — their most advanced clinical program with EUR 2.5M in EC funding.
  • PACE
    Largest single EC contribution (EUR 3.1M) — a multicenter Phase IIb study that generated the clinical evidence foundation for the Phase III follow-up.
  • nTRACK
    Unusual cross-sector project combining nanotechnology with stem cell therapy, developing imaging nanoparticles to track cell therapy effectiveness in vivo.
Cross-sector capabilities
Regenerative medicine and orthopaedicsNanomedicine and in-vivo imagingAdvanced therapy manufacturing (biologics)Clinical trial design and regulatory science
Analysis note: Strong profile despite only 4 projects — the projects are thematically coherent, well-funded (avg EUR 1.5M), and show clear clinical progression from Phase IIb to Phase III. Company rebranded from Pluristem Therapeutics to Pluri Inc/Pluri Biotech; the website URL (pluristem.com) reflects the earlier name.