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Forte Biosciences (FBRX) investor relations material
Forte Biosciences Q3 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
FB102 advanced with positive Phase 1b celiac disease data; Phase 2 celiac and Phase 1b vitiligo and alopecia areata trials ongoing, with topline data for all three expected in 2026.
US IND for FB102 is open, enabling expanded enrollment in the celiac disease Phase 2 trial at US sites.
$93.4 million in cash and cash equivalents as of September 30, 2025, following $75 million public offering and $53 million private placement.
No commercial revenue; focus remains on clinical development and expanding indications for FB102.
Financial highlights
Net loss of $17.7 million for Q3 2025, up from $8.4 million in Q3 2024; net loss of $44.6 million for the nine months ended September 30, 2025, compared to $28.3 million in the prior year period.
Research and development expenses rose to $15.2 million in Q3 2025 (from $5.9 million in Q3 2024), mainly due to increased clinical and manufacturing costs.
General and administrative expenses were $3.2 million in Q3 2025 (up from $2.8 million), driven by higher personnel costs.
Net loss per share was $(0.99) for Q3 2025 versus $(4.54) for Q3 2024; for the nine months ended September 30, 2025, net loss per share was $(3.26) compared to $(15.35) in 2024.
Ended Q3 2025 with $93.4 million in cash and cash equivalents.
Outlook and guidance
Topline results for FB102 in celiac disease, vitiligo, and alopecia areata expected in 2026.
Cash runway expected to fund operations for at least 12 months from the filing date.
Additional capital will be required to complete development and commercialization of FB102.
R&D expenses may increase as clinical programs expand and new indications are pursued.
General and administrative expenses may fluctuate with infrastructure and advisory needs.
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