FUBIS (Floxuridine-Alendronate) First-in-class bone-targeted chemotherapy

Preclinical · Advancing toward first-in-human study

A single agent that combines tumor cell kill and bone preservation — delivering chemotherapy directly to bone metastases while protecting healthy bone.

0patients affected each year in the US & EU
0reduction in metastatic burden (preclinical)
0increase in new bone generated (preclinical)
0of breast & prostate cancer patients develop bone metastases
The challenge

A severe disease burden that calls for better therapies

Bone is one of the most common places for cancer to spread. Once tumor cells settle in bone, they disrupt its natural balance — causing pain, fractures and a major loss in quality of life.

0patients in the US and EU live with bone metastases each year(1)
0of breast and prostate cancer patients develop bone metastases(2)
0global market for bone metastasis therapy
0expected annual market growth (CAGR)

What patients face

“Bone metastases are a major cause of morbidity.”(2) Select a complication to learn more.

First-in-class bone-targeted chemotherapy addressing a multi-billion unmet need in bone metastases

1) Extrapolated from: Hernandez et al., Incidence of bone metastases in patients with solid tumors, BMC Cancer (2018) 18:44. 2) Oncology Reviews 2017; 11:321.

What is FUBIS

Two proven drugs, joined into one bone-seeking molecule

Bisphosphonates strengthen bone. Chemotherapy destroys cancer cells. Decades of efforts to effectively combine the two failed — FUBIS joins them in a single bone-targeted duplex drug.

Alendronate bone-seeking Floxuridine 5-FdU · tumor-killing

👆 Tap a part of the molecule

Multi-billion market in bone metastases

First-in-class bone-targeted duplex drug platform

De-risked components: approved drugs Alendronate + 5-FdU

Validated preclinical proof-of-concept — efficacy and safety

Highly experienced team of leading oncology experts & institutions

At clinical inflection point — ~€10m required to advance to first-in-human

Explainer film

FUBIS in two and a half minutes

Follow the story of a patient with bone metastases — and see how FUBIS finds the tumor in bone, breaks it down, and helps rebuild the bone. Jump to any chapter.

Chapters

Mechanism of action

Dual mechanism: inhibiting bone resorption and eliminating tumor cells

Explore the four steps by tapping the numbers on the illustration or the cards — or press play to walk through them automatically.

Illustration of the bone microenvironment with tumor cells, osteoclasts and osteoblasts

Mechanism

How FUBIS acts
  • Localized, targeted activity at metastatic sites
  • Direct disruption of tumor–bone interaction
  • Inhibition of osteoclast-driven bone resorption
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Preclinical findings

What we've observed
  • Reduced metastatic burden in preclinical models
  • Increased new bone generated in preclinical models
  • Preclinical evidence supporting further clinical evaluation
›

Potential patient relevance

Subject to clinical validation
  • Potential to reduce pain and analgesic need
  • Potential to support mobility and daily function
  • Potential quality-of-life benefits
Bone-targeted therapeutic approach – to be clinically evaluated
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Why a new approach is needed

FUBIS is an investigational, preclinical-stage compound. Its potential benefits are subject to clinical validation.

Preclinical evidence

Strong efficacy and safety in bone metastases models

A unique combination of targeted efficacy and a favourable preclinical safety profile.

0reduction in metastatic burden
0increase in new bone generated
0observed systemic toxicity
Market opportunity

A large, growing market with significant unmet need

Market reality

  • ~1.2 million patients in US & EU annually
  • >$20bn global market, growing at ~8–10% CAGR
  • Up to 70% of advanced breast & prostate cancers develop bone metastases

Current treatment gap

  • Focus on bone protection, not tumor elimination
  • Limited impact on disease progression
  • Ongoing pain, fractures and quality-of-life burden

Why FUBIS matters

  • Dual mechanism: tumor cell kill + bone preservation
  • Targeted delivery to metastatic bone sites
  • Potential for disease-modifying effect, not just symptom control
Development supported by established partners (e.g. Charles River, UKSH)
~€15m invested into preclinical development and platform build-up
+
GLP tox, PK/PD and mode-of-action studies completed / ongoing
+
Validated preclinical proof-of-concept (efficacy + safety)
Development roadmap

A compelling opportunity at a clinical inflection point

Select a stage to see what it involves.

Series A

financing round to advance FUBIS through combined Phase 1/2 clinical development

Transaction structure

  • Limited, preferential secondary share allocation for participating investors
  • Fixed pro rata calculation
  • Equity share and price negotiated directly with the patent holder

Use of funds

  • CTA-enabling development
  • Phase 1/2 clinical execution

Target

  • Series B financing following combined Phase 1/2 proof of concept
Investment highlights

Key value drivers for FUBIS

Tap a level of the pyramid to explore each value driver.

The Pekkip Oncology Alliance team

Clinical, scientific and healthcare entrepreneurship expertise

Strong access to clinical infrastructure and patient pathways through established partnerships (e.g. UKSH)
FAQ

Frequently asked questions

Partner with us to bring FUBIS to patients

We are raising a Series A to take FUBIS through combined Phase 1/2 clinical development. Get in touch to receive the full investment materials.

Email: werlephilip@gmail.com

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