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 beg early 2024 (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