First Tracks Biotherapeutics Announces Second Quarter 2026 Financial Results and Provides Business Update
Rhea-AI Summary
First Tracks Biotherapeutics (Nasdaq: TRAX) reported second quarter 2026 results and updated progress across its pipeline. Lead asset ANB033/b) received U.S. FDA Fast Track designation for celiac disease and completed enrollment of Cohort 1 in its Phase 1b gluten‑challenge trial, with top‑line data reaffirmed for Q4 2026 and Cohort 2 mucosal‑healing data expected in Q1 2027. A separate 50‑patient Phase 1b trial in eosinophilic esophagitis is enrolling, with top‑line data anticipated in Q3 2027. ANB101’s Phase 1a in healthy volunteers is complete, while strategic options are being evaluated for rosnilimab. Following its April 20, 2026 separation from AnaptysBio, the company reported
Positive
- Cash, cash equivalents and investments $168.0M as of June 30, 2026; runway into Q2 2028
- R&D expenses reduced to $25.6M in Q2 2026 from $39.3M in Q2 2025
- Net loss improved to $33.4M in Q2 2026 from $42.4M in Q2 2025
- U.S. FDA granted Fast Track designation to ANB033 for treatment of celiac disease
- Phase 1b ANB033 Cohort 1 enrollment completed; data expected Q4 2026
- Phase 1a trial of ANB101 completed in healthy volunteers
Negative
- Net loss $83.9M for the six months ended June 30, 2026
- G&A expenses increased to $9.3M in Q2 2026 from $6.6M in Q2 2025
- Total assets declined to $183.1M at June 30, 2026 from $330.5M at December 31, 2025
News Explained
Q2 financials still include combined-company allocations through April 19, 2026, so the six-month expense history is not wholly standalone.
The First Tracks Biotherapeutics separation from AnaptysBio was completed on
However, the reported 2026 six-month results include assets, liabilities, and expenses of both companies through
The disclosed share count establishes a post-separation common-equity structure, but it does not by itself establish how any existing holder's percentage ownership changed.
The next specified clinical checkpoints are top-line Cohort 1 celiac-disease data in
Market reaction after 2Q26 earnings report: TRAX -4.55% in the Aug 13 session
In the Aug 13 session, TRAX declined 4.55%, reflecting a moderate negative market reaction. Argus tracked a trough of -2.3% from its starting point during tracking. Our momentum scanner triggered 21 alerts that day, indicating elevated trading interest and price volatility.
Data tracked by StockTitan Argus on the day of publication.
Key Figures
Previous Earnings Reports
| Date | Event | Sentiment | 24h Move | Catalyst |
|---|---|---|---|---|
| May 14 | Q1 earnings report | Negative | -6.9% | Reported net loss alongside higher general and administrative expenses after separation. |
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
The tag-specific record shows the prior earnings event followed by a -6.94% 24-hour reaction.
Key Terms
fast track designation regulatory
cd122 antagonist medical
histologic medical
AI-generated analysis. How Rhea-AI works. Not financial advice.
- Completed enrollment for Cohort 1 (gluten challenge) of Phase 1b ANB033 trial in celiac disease (CeD); top-line Cohort 1 data reaffirmed for Q4 2026
- Cohort 2 (mucosal healing) enhanced to enroll up to 40 patients including those with a broad range of histologic (Vh:Cd ratio ≤ 2.5) and symptom severity to further inform future development; top-line Cohort 2 data anticipated in Q1 2027
- U.S. FDA granted Fast Track designation for ANB033 for the treatment of CeD
- Enrollment ongoing for Phase 1b ANB033 trial in eosinophilic esophagitis (EoE); top-line data anticipated in Q3 2027
- Reiterating cash-runway into Q2 2028, including the expansion of ANB033 into two additional indications in H1 2027
SAN DIEGO, Aug. 12, 2026 (GLOBE NEWSWIRE) -- First Tracks Biotherapeutics, Inc. (Nasdaq: TRAX), a clinical-stage biotechnology company advancing antibody therapeutics that modulate immune pathways implicated in autoimmune and inflammatory diseases, today reported financial results for the second quarter ended June 30, 2026, and provided a business update.
“First Tracks continues to execute against a broad development strategy for our potentially best-in-class CD122 antagonist, ANB033, and anticipates treating patients across four indications in 2027. We believe ANB033 is uniquely positioned to deliver differentiated clinical and biological outcomes across multiple immune-mediated diseases,” said Daniel Faga, president and chief executive officer. “In celiac disease, FDA’s Fast Track designation for ANB033 underscores both the urgency of the significant unmet need for patients and the potential of this program. We will report top-line data from Cohort 1 of the Phase 1b trial in Q4 2026, evaluating ANB033's potential to prevent gluten-induced mucosal injury. Cohort 2 of this study is enrolling patients with disease across a wide range of histologic and symptom severity at baseline with the goal of generating deeper insights into timing to mucosal healing and disease biology. We anticipate reporting these data in Q1 2027, followed by top-line data from our Phase 1b trial of ANB033 in eosinophilic esophagitis in Q3 2027.”
ANB033 (CD122 antagonist)
- Phase 1b trial in celiac disease ongoing
- U.S. FDA granted Fast Track designation to ANB033 for the treatment of people with CeD on a gluten-free diet
- 70-patient trial assessing one dose level of subcutaneously administered ANB033 vs. placebo (randomized 1:1) across two different cohorts
- Cohort 1 (n=30) is a gluten-challenge study to assess the prevention of mucosal damage through six weeks
- Top-line Cohort 1 data reaffirmed for Q4 2026
- Cohort 2 (n=40) assesses the possibility of mucosal healing through 12 weeks
- Cohort enhanced to enroll up to 40 patients including those with a broad range of histologic (Vh:Cd ratio ≤ 2.5) and symptom severity to further inform future development
- Enrollment ongoing with top-line Cohort 2 data anticipated in Q1 2027
- Cohort 1 (n=30) is a gluten-challenge study to assess the prevention of mucosal damage through six weeks
- Phase 1b trial in EoE ongoing
- 50-patient cohort assessing one dose level of subcutaneously administered ANB033 vs. placebo (randomized 1:1) through 12 weeks
- Top-line Phase 1b data anticipated in Q3 2027
- Plan to initiate Phase 2 trials in two additional indications in H1 2027
ANB101 (BDCA2 modulator)
- Phase 1a trial in healthy volunteers completed
- Currently evaluating potential development approach informed by clinical and translational evidence, as well as competitor registrational data in systemic lupus erythematosus (SLE) and cutaneous lupus erythematosus (CLE) anticipated in Q4 2026 and early 2027, respectively
- Currently evaluating potential development approach informed by clinical and translational evidence, as well as competitor registrational data in systemic lupus erythematosus (SLE) and cutaneous lupus erythematosus (CLE) anticipated in Q4 2026 and early 2027, respectively
Rosnilimab (Pathogenic T cell depleter)
- Currently assessing ROE-maximizing strategic options to progress the potential development of rosnilimab in rheumatoid arthritis (RA) and other indications
Second Quarter 2026 Financial Results
- The separation of AnaptysBio and First Tracks Biotherapeutics was completed on April 20, 2026. As a result, from January 1, 2026 to April 19, 2026 and the three and six months ended June 30, 2025, the financial results include assets, liabilities and expenses related to both companies. The combined financial statements reflect allocations of certain expenses from the financial statements of Anaptys including research and development expenses and administrative expenses. These allocations include, but are not limited to, executive management, employee compensation and benefits, facilities and operations, information technology, business development, financial services (such as accounting, audit, and tax), legal, insurance and stock-based compensation.
- Cash, cash equivalents and investments totaled
$168.0 million as of June 30, 2026. - Research and development expenses were
$25.6 million and$59.6 million for the three and six months ended June 30, 2026, compared to$39.3 million and$80.7 million for the three and six months ended June 30, 2025. The decrease for the three and six months ended June 30, 2026 was primarily due to decreased development costs for rosnilimab and ANB032 offset by increased costs relating to the Phase 1 trials for ANB033. - General and administrative expenses were
$9.3 million and$28.1 million for the three and six months ended June 30, 2026, compared to$6.6 million and$16.4 for the three and six months ended June 30, 2025. The increase was due primarily to the allocation of legal costs for the separation of the company. - Net loss was
$33.4 million and$83.9 million for the three and six months ended June 30, 2026, or a net loss per share of$0.95 and$2.40 , compared to a net loss of$42.4 million and$89.6 million for the three and six months ended June 30, 2025, or a net loss per share of$1.47 and$3.02 .
About First Tracks Biotherapeutics
First Tracks Biotherapeutics is a clinical stage biotechnology company advancing antibody therapies that modulate immune pathways implicated in autoimmune and inflammatory diseases. Its pipeline includes ANB033, a CD122 antagonist in development for celiac disease and eosinophilic esophagitis; rosnilimab, a pathogenic T cell depleter in development for rheumatoid arthritis; and ANB101, a BDCA2 modulator. To learn more, visit www.FirstTracksBio.com or follow us on LinkedIn.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995, including, but not limited to: the timing of the release of data from the Company’s clinical trials, including initial data from ANB033's Phase 1b clinical trial in celiac disease and initial data from ANB033's Phase 1b clinical trial in eosinophilic esophagitis; potential benefits, efficacy, and safety profile of the Company’s product candidates and the Company’s projected cash runway. Statements including words such as “plan,” “continue,” “expect,” or “ongoing” and statements in the future tense are forward-looking statements. These forward-looking statements involve risks and uncertainties, as well as assumptions, which, if they do not fully materialize or prove incorrect, could cause its results to differ materially from those expressed or implied by such forward-looking statements. Forward-looking statements are subject to risks and uncertainties that may cause the company’s actual activities or results to differ significantly from those expressed in any forward-looking statement, including risks and uncertainties related to the company’s ability to advance its product candidates, obtain regulatory approval of and ultimately commercialize its product candidates, the timing and results of preclinical and clinical trials, the company’s ability to fund development activities and achieve development goals, the company’s ability to protect intellectual property and other risks and uncertainties described under the heading “Risk Factors” in documents the company files from time to time with the Securities and Exchange Commission. These forward-looking statements speak only as of the date of this press release, and the company undertakes no obligation to revise or update any forward-looking statements to reflect events or circumstances after the date hereof.
Investor Contact:
Nick Montemarano
Vice President, Investor Relations
858.732.0178
investors@firsttracksbio.com
| First Tracks Biotherapeutics, Inc. Balance Sheets (in thousands, except share and par value) (unaudited) | ||||||||
| June 30, 2026 | December 31, 2025 | |||||||
| ASSETS | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 168,018 | $ | 238,196 | ||||
| Short-term investments | — | 73,442 | ||||||
| Prepaid expenses and other current assets | 9,727 | 4,762 | ||||||
| Total current assets | 177,745 | 316,400 | ||||||
| Property and equipment, net | 1,071 | 1,370 | ||||||
| Operating lease right-of-use assets | 4,324 | 12,519 | ||||||
| Other long-term assets | — | 256 | ||||||
| Total assets | $ | 183,140 | $ | 330,545 | ||||
| LIABILITIES AND STOCKHOLDERS’ EQUITY | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 2,553 | $ | 3,111 | ||||
| Accrued expenses | 7,458 | 25,832 | ||||||
| Current portion of operating lease liability | 2,436 | 2,080 | ||||||
| Total current liabilities | 12,447 | 31,023 | ||||||
| Operating lease liability, net of current portion | 1,897 | 12,032 | ||||||
| Stockholders’ equity: | ||||||||
| Preferred stock | — | — | ||||||
| Common stock, | 35 | — | ||||||
| Additional paid-in capital | 193,337 | — | ||||||
| Accumulated other comprehensive loss | — | (24 | ) | |||||
| Accumulated deficit | (24,576 | ) | — | |||||
| Net former parent investment | — | 287,514 | ||||||
| Total stockholders’ equity | 168,796 | 287,490 | ||||||
| Total liabilities and stockholders’ equity | $ | 183,140 | $ | 330,545 | ||||
| First Tracks Biotherapeutics, Inc. Statements of Operations and Comprehensive Loss (in thousands) (unaudited) | ||||||||||||||||
| Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
| 2026 | 2025 | 2026 | 2025 | |||||||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | 25,644 | 39,272 | 59,599 | 80,737 | ||||||||||||
| General and administrative | 9,293 | 6,626 | 28,149 | 16,441 | ||||||||||||
| Total operating expenses | 34,937 | 45,898 | 87,748 | 97,178 | ||||||||||||
| Loss from operations | (34,937 | ) | (45,898 | ) | (87,748 | ) | (97,178 | ) | ||||||||
| Other income (expense), net: | ||||||||||||||||
| Interest income | 1,564 | 3,466 | 3,892 | 7,557 | ||||||||||||
| Other expense, net | (1 | ) | (13 | ) | (2 | ) | (20 | ) | ||||||||
| Total other income (expense), net | 1,563 | 3,453 | 3,890 | 7,537 | ||||||||||||
| Net loss | (33,374 | ) | (42,445 | ) | (83,858 | ) | (89,641 | ) | ||||||||
| Other comprehensive loss: | ||||||||||||||||
| Unrealized gain (loss) on available-for-sale securities | 146 | (167 | ) | 24 | (311 | ) | ||||||||||
| Comprehensive loss | $ | (33,228 | ) | $ | (42,612 | ) | $ | (83,834 | ) | $ | (89,952 | ) | ||||
| Net loss per common share: | ||||||||||||||||
| Basic and diluted | $ | (0.95 | ) | $ | (1.47 | ) | $ | (2.40 | ) | $ | (3.02 | ) | ||||
| Weighted-average number of shares outstanding: | ||||||||||||||||
| Basic and diluted | 35,003 | 28,810 | 35,003 | 29,722 | ||||||||||||
