STC 1010

Our first candidate in metastatic colorectal cancer

An allogeneic first in class immunotherapy harnessing the patient immune system to fight immune tolerance and prevent cancer resistance

Phase I/II 1L mCRC study synopsis validated

Launch in 2025 (US, BEL, FR)

An allogeneic first in class immunotherapy harnessing the patient immune system to fight immune tolerance and prevent cancer resistance

Phase I/II 1L mCRC study synopsis validated

Launch beg early 2024 (US, BEL, FR)

High unmet need

2nd cause

of cancer mortality worldwide

608.000

Patients in 2029 WW

95%

of patients treated by chemotherapies in 1L inducing toxicity, resistances, and tumor plasticity.

Big Pharmas face a patent cliff

For Standard of care : Pembrolizumab, Atezolizumab, Nivolumab, Ipilimumab (within 2028)

Our product

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Our response

01.

To meet the need in targeting treatment resistance

STC-1010 targets MSS and MSI-H population.
02.

To meet the need in breaking immunue tolerance

STC-1010 has a robust and validated preclinical data pack showing:

INCREASE IN OVERALL SURVIVAL

in colorectal cold and hot mice model

INCREASE IN CD8+ TUMOR INFILTRATION

in several model

EFFICACY IN ANTI-PD1 RESISTANT

mice model

03.

To meet the need for an accessible approach

An OFF-THE-SHELF technology allowing control of both time and cost of the manufacturing process.

Stc1010, the missing link ? A biological rational

Adapted from C. Cremolini ESMO 2021

Exemple of treatments with a biological rational to combine with STC 1010
Step 1

GM-CSF low dose: Recruits APC at injection point and mature DCs.

Step 2

Checkpoint inhibitors, ADC TLR Promotes T cell priming and activation

Step 3

Chemokyne cytokine TLR : Increase trafficking of T cell

Step 4

Bevacizumab Facilitates infiltration of CD8+ lymphocytes into tumors

Step 5

5FU, Bevacizumab and Cyclophosphamide low dose, radiotherapy. Decrease the activity of immunosuppressive cells (Tregs and MDSCs)

Step 6

Checkpoint inhibitors, ADC, BiSpecific mAb, TLR restores the anticancer immunity

AT BRENUS, WE AIM TO CHANGE A PARADIGM IN ONCOLOGY

INCREASE IMMUNOGENICITY

Brenus’ manufacturing process overpasses the lack of immunogenicity & educates the immune system  with visible and multi-specific targets

REPRESENT HETEROGENEITY OF THE TARGETED INDICATION

Selection criteria of starting material (Allogeneic tumor cell lines)

  • Representative oncogenic drivers (TP53,BRAF,KRAS,…)
  • Cold & hot tumor cell lines
  • Resistances capacities (metabolic ; chemical & physical)

Increase antigenicity

Brenus’ manufacturing process overpasses the lack of antigenicity & educates the immune system  with broad & higher quality range of tumor antigens