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Analyst Comment

Faron’s anticipated opening in solid tumors

By Antti SiltanenAnalyst
Faron Pharmaceuticals

Summary

  • Faron is expanding its clinical development program for bexmarilimab to include solid tumors, specifically through the investigator-initiated BEXAR study targeting soft tissue sarcoma.
  • The BEXAR study, a randomized Phase I/II trial, will evaluate the combination of bexmarilimab and doxorubicin, with funding from MEDSIR and collaboration with University Hospital Vall d’Hebron.
  • The trial aims to address the significant medical need in soft tissue sarcomas, which are often immunologically inactive, by potentially reprogramming tumor macrophages to improve treatment efficacy.
  • Faron's strategic use of investigator-initiated trials allows for cost-effective collection of clinical evidence, aligning with its focus on blood cancers and the need to secure funding for the BEXMAB-02 trial.

This content is generated by AI. You can give feedback on it in the Inderes forum.

Translation: Original published in Finnish on 1/28/2026 at 7:00 am EET.

Faron announced on Tuesday that it is expanding the clinical development program for bexmarilimab to solid tumors. The company is supporting a new investigator-initiated phase I/II BEXAR study, which will investigate the tolerability, safety, and preliminary efficacy of the drug candidate in soft tissue sarcoma in combination with standard treatment. The news marks Faron's first concrete opening in solid tumors since the MATINS study. The company announced its plans for BEXAR at the CMD in fall 2024, so the start of the study was expected.

Bexmarilimab is now being studied in soft tissue sarcoma

Faron announced in a press release that it is expanding bexmarilimab's clinical program by supporting the investigator-initiated BEXAR study. Investigator-initiated trials are based on academic interest and are not usually designed in cooperation with the regulatory authority from the perspective of meeting the requirements for a marketing authorization application. However, they provide useful information that can advance commercialization opportunities and are cost-effective to implement from Faron's perspective. The randomized design of the trial is also a qualitative advantage.

This is a randomized Phase I/II trial evaluating the combination of bexmarilimab and the standard-of-care chemotherapy doxorubicin in patients with metastatic soft tissue sarcoma. The trial is funded (i.e. "sponsored") by MEDSIR, which specializes in oncology research, and is conducted in collaboration with University Hospital Vall d’Hebron in Barcelona. Due to the early research phase, potential commercialization in soft tissue sarcoma is not expected until around the mid-2030s.

The expansion into soft tissue sarcoma is biologically justified, as these tumors often show expression of bexmarilimab's target protein, Clever-1. Soft tissue sarcomas are often immunologically inactive, or "cold." Therefore, common cancer drugs, immune checkpoint inhibitors, work poorly in them. There is a significant medical need in these cancers. Sarcomas are characterized by an immunosuppressive microenvironment where macrophage cells inhibit the function of the immune system. The aim of the trial is to clarify whether bexmarilimab can reprogram tumor macrophages, turn the tumor into an immunologically "hot" tumor, and thus improve treatment efficacy.

The investigator-initiated trial (IIT) approach supports the strategy

Faron's development focus has recently shifted strongly towards blood cancers, and the company aims to initiate a pivotal Phase II/III BEXMAB-02 registration trial in high-risk MDS patients this year. Regarding solid tumors, Faron published an updated development plan at the CMD in fall 2024. The updated strategy introduced BEXAR and other solid tumor projects. Thus, the news of BEXAR's initiation did not come as a surprise. The investigator-initiated trial (IIT) approach is strategically sound for the company, as it allows for the collection of clinical evidence in new indications at a low cost from Faron's perspective. Faron's next key task is to secure funding for the BEXMAB-02 trial. Based on current information, the company would not have the resources to finance solid tumor trials itself, so the investigator-initiated model is logical for the company.

 

Faron is a global, clinical-stage biopharmaceutical company, focused on tackling cancers via novel immunotherapies. Its mission is to bring the promise of immunotherapy to a broader population by uncovering novel ways to control and harness the power of the immune system. The Company's lead asset is bexmarilimab, a novel anti-Clever-1 humanized antibody, with the potential to remove immunosuppression of cancers through reprogramming myeloid cell function. Bexmarilimab is being investigated in Phase I/II clinical trials as a potential therapy for patients with hematological cancers in combination with other standard treatments.

Read more on company page

Key Estimate Figures2025-10-24

202425e26e
Revenue0.00.00.0
growth-%
EBIT (adj.)-18.7-22.6-30.5
EBIT-% (adj.)-466,750.0 %-565,225.0 %-762,390.0 %
EPS (adj.)-0.25-0.22-0.28
Dividend0.000.000.00
Dividend %
P/E (adj.)neg.neg.neg.
EV/EBITDAneg.neg.neg.

Forum discussions

I examined this a bit critically and also made my own corresponding calculation. There are a couple of things I disagree with you on, and they...
1 hour ago
by OsakasOssi
3
NPV 4.8B, from which Faron gets 10% royalties. Total p for market entry: 50% Phase 2 x 50% Phase 3 x 90% FDA approval. This calculation assumes...
2 hours ago
by Clark kent
3
Did you calculate in your example that approval occurs with a 10% probability? Was that intentional - or were you supposed to calculate with...
2 hours ago
by SOJ
1
You can make a model like that look however you want. But I’ve used very generous assumptions just as a basis for discussion. My own % assumptions...
4 hours ago
by Clark kent
17
No, because every Big Pharma company first wants certainty that OS is removed from the endpoints. Clark Kent wrote about the procedure with ...
4 hours ago
1
It’s starting to get restless again. Let’s refine this model in light of current knowledge. Let’s set some quite GENEROUS assumptions for now...
5 hours ago
by Clark kent
14
My father used to say about “what ifs” that if your aunt were your uncle, she’d have… She isn’t, however—at least not yet—so if a shareholder...
6 hours ago
by Vino Pino
41
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