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Forte Biosciences (FBRX) investor relations material
Forte Biosciences Q2 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Lead candidate FB102 advanced in clinical trials for celiac disease, vitiligo, and alopecia areata, with positive Phase 1b data in celiac and vitiligo and Phase 2 and 1b trials ongoing; topline readouts expected in H2 2026.
Entered into a definitive merger agreement with argenx BV for acquisition at $77.00 per share in cash, pending customary closing conditions.
Raised $172.5 million in April 2026 and $75 million in June 2025 through public offerings to fund clinical development.
Financial highlights
Cash, cash equivalents, and short-term investments totaled $198.5 million as of June 30, 2026.
Net loss was $45.5 million for the six months ended June 30, 2026, compared to $26.9 million for the same period in 2025.
Research and development expenses rose to $42.8 million for the six months ended June 30, 2026, up from $21.3 million year-over-year, driven by increased clinical activity and headcount.
General and administrative expenses decreased to $4.2 million for the six months ended June 30, 2026, from $6.4 million in 2025, primarily due to $4.8 million in legal settlement payments.
Net cash used in operating activities was $41.5 million for the six months ended June 30, 2026.
Outlook and guidance
Existing cash and investments expected to fund operations for at least twelve months from the filing date.
Ongoing clinical trials for FB102 in celiac disease (Phase 2) and alopecia areata (Phase 1b) with topline data expected in H2 2026.
Future capital requirements will depend on clinical progress, regulatory outcomes, and potential strategic transactions.
- FB102 shows strong efficacy and safety in celiac disease, with broad potential in autoimmune therapy.FBRX
Corporate presentation - FB102 produced significant, durable repigmentation in vitiligo with strong safety and outperformed JAK inhibitors.FBRX
Study result - Biotech seeks up to $500M for autoimmune drug pipeline, targeting major unmet needs.FBRX
Registration filing - Shelf registration enables up to $500M in offerings to fund autoimmune drug development.FBRX
Registration filing - FB102 won FDA Fast Track, posted $22.1M Q1 loss, and raised $172.5M to fund clinical trials.FBRX
Q1 2026 - Key votes include director elections, auditor ratification, say-on-pay, and equity plan expansion.FBRX
Proxy filing - FB102 clinical trials progress, R&D costs surge, and net loss widens amid strong cash position.FBRX
Q4 2025 - Registering 9.5M shares for resale post-$53M private placement; focus on autoimmune therapies.FBRX
Registration Filing - FB102 showed significant histological and symptom benefits with good safety in celiac disease.FBRX
Study Update
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