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Analyst Comment

Faron Phase I/II BEXMAB trial patient enrollment completed; topline readout postponed to April

By Antti LuiroHead of Nordic ER Development, Analyst
Faron Pharmaceuticals

Translation: Original published in Finnish on 1/31/2025 at 4:11 pm EET.

Faron announced that it has identified the last patient for the Phase II BEXMAB study and now expects the topline readout in April. As a result, patient enrollment was completed in January as previously announced, although the topline response rate readout was bumped slightly forward from the end of Q1'25 as previously announced.

The financing solution is tilting towards equity financing

According to the company, Faron has sufficient cash resources for the end of Q2'25. Without breaching the terms of the loan, cash will be sufficient until the end of Q1'25 at the latest when additional financing will be required. We believe that a partnership agreement or an equity financing round are the most likely financing options for the company. We expect Faron to seek a partnership agreement only after the topline readout, and it being postponed tips the scales more clearly in favor of equity financing. Supported by the positive results of the BEXMAB trial to date, the company is in a good position to raise funds, so we do not see any particular concerns. We will review our view of the company no later than the time of the publication of the financial statements at the end of February.

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 Figures2024-12-11

202324e25e
Revenue0.00.00.0
growth-%
EBIT (adj.)-28.6-26.1-29.2
EBIT-% (adj.)-714,200.0 %-653,250.0 %-730,500.0 %
EPS (adj.)-0.45-0.28-0.30
Dividend0.000.000.00
Dividend %
P/E (adj.)neg.neg.neg.
EV/EBITDAneg.neg.neg.

Forum discussions

https://submit.hematology.org/program/presentation/671797 ASH’s real-world MDS data from 1429 patients makes for grim reading, showing how weak...
3 hours ago
by poiju
9
bex + chemotherapy patents.google.com WO2025141246A1 - Clever-1 inhibitor for promoting hematological recovery when... The present invention...
4 hours ago
by Koodinikkari
12
And by no means should conference buzz alone be considered the sole basis for investment. But it does give me enough validation for the data...
4 hours ago
by samunho
5
Keep in mind that congress presentations are a species of their own. Especially for getting into an oral presentation, the “buzz factor” matters...
4 hours ago
by Clark kent
2
Are any new numerical results expected in that Tuesday morning’s ASH/Kontro presentation, or does it only generally reflect the follow-ups made...
6 hours ago
by Kulkuri
3
This is a Yale professor. He is indeed one of Faron’s scientific advisors, but he is not solely an employee of Faron. He is likely involved ...
7 hours ago
by Ville Kuoksa
12
In my opinion, the essential observations: R/R mOS increased to 14.5 months Now, different subgroups are better understood, which is important...
7 hours ago
16
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