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Seaport Therapeutics Holds $403.8 Million, Enough Cash to Run Into 2029

Seaport Therapeutics ended Q3 with $403.8 million in cash, up 73% since December, and says it is funded into 2029. Its net loss widened 17% to $26.4 million.

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Streets and buildings of Boston's Seaport District at twilight, March 2019
Boston’s Seaport District, where Seaport Therapeutics is based, at twilight in March 2019. The photo shows the neighborhood, not the company. Photo: Sergey Galyonkin, Wikimedia Commons, CC BY-SA 2.0 (file photo).

Seaport Therapeutics ended September with $403.8 million in cash, cash equivalents and investments. That is 73% more than it held at the end of 2025, and the Boston drug developer says the money will last into 2029. The company reported third-quarter results Monday, Nov. 2, six months after it went public on Nasdaq. Its net loss widened 17% to $26.4 million, according to the results release filed with the SEC.

Seaport (Nasdaq: SPTX) develops oral medicines for depression, anxiety and other neuropsychiatric disorders. The company said its cash runway covers three mid-to-late-stage clinical readouts. The first is expected in the first half of 2027, from a Phase 2b trial of its lead drug in major depressive disorder.

Key figures: Cash and investments $403.8M · Q3 net loss $26.4M ($0.49/share) · R&D $23.9M (up 17%) · G&A $6.5M (up 29%) · Runway into 2029

The quarter by the numbers

Research and development spending rose to $23.9 million from $20.5 million a year earlier. Seaport said the $3.4 million increase came mainly from its BUOY-1 Phase 2b trial. General and administrative costs rose to $6.5 million from $5.0 million, which the company tied mainly to the costs of operating as a public company. Total operating expenses were $30.3 million, up from $25.4 million, according to the Form 8-K filing.

The net loss per share fell to $0.49 from $9.43, even though the dollar loss grew. That is because the share count changed after the IPO: weighted-average shares outstanding rose from about 2.4 million to about 53.5 million. Other income, mostly from the cash pile, added $4.1 million in the quarter.

For the first nine months of 2026, the net loss was $114.4 million, compared with $50.7 million a year earlier. Most of that gap came from general and administrative costs, which reached $53.8 million for the nine months. That figure includes $39.1 million of non-cash stock-based compensation, compared with $3.5 million in the same period of 2025.

Data analysis: spending up, runway longer

The Boston Report compared the third quarter with the same quarter of 2025, using the company’s reported figures. R&D and the net loss each grew about 17%, and G&A grew about 29%. R&D was 79% of operating expenses, roughly the same share as a year earlier (80%). The extra spending is going mostly to clinical work, not overhead.

Bar chart of Seaport Therapeutics third-quarter results: R&D expense rose 17% to $23.9 million, G&A expense rose 29% to $6.5 million and net loss widened 17% to $26.4 million versus Q3 2025.
Source: Seaport Therapeutics Q3 2026 results, SEC Form 8-K Exhibit 99.1 (Nov. 2, 2026); percent changes are TBR calculations; chart: The Boston Report.

The cash balance rose $170.1 million from $233.7 million on Dec. 31, 2025. The main reason was the initial public offering. On April 30, Seaport priced an upsized IPO of about 14.2 million shares at $18 each, raising about $254.9 million before fees. Its shares began trading May 1. At the third quarter’s operating-expense pace of about $30 million, the balance equals a little over three years of spending, in line with the company’s guidance of funding into 2029. That simple estimate does not account for future changes in trial costs.

Pipeline milestones

  • GlyphAllo (SPT-300), major depressive disorder: In September, a Phase 1 driving-simulation trial met its main goal. An evening dose of 375 mg did not impair next-morning driving compared with placebo, and the company plans to submit the results to the FDA. Enrollment in the Phase 2b BUOY-1 trial is on track, with topline data expected in the first half of 2027.
  • GlyphAgo (SPT-320), generalized anxiety disorder: The first patient was dosed in October in a Phase 2a trial in patients with anxiety and sleep disturbance, with data expected in early 2028. A Phase 2/3 trial is planned for the first half of 2027, with data by the end of 2028. Earlier data showed a 6.8-fold increase in agomelatine bioavailability, the company said.
  • Glyph2BLSD (SPT-348): This non-hallucinogenic version of a psychedelic compound is in preclinical work. First-in-human-enabling studies are expected to finish by the end of 2027.

A Seaport District biotech

The company is based in Boston’s Seaport District, the South Boston waterfront neighborhood that is also home to other life sciences companies. Its results join a busy Boston earnings season, which we track in our roundup of third-quarter earnings from Boston companies. The local biotech IPO market has stayed active, too: Bambusa Therapeutics recently made its Nasdaq debut. For more company coverage, see the business section of our Boston news page.

“Seaport is well-capitalized, with cash runway through all three of our upcoming mid-to-late-stage clinical data readouts,” co-founder and CEO Daphne Zohar said in the release. “There are a billion people living with mental illness – waiting and hoping for better medicines.”

The company noted that clinical results are uncertain. Its forward-looking statements list risks including trial outcomes, regulatory review and the need for more funding.

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