Tempest Therapeutics Q2 loss narrows to $5.2m; advances CAR-T pipeline

3 min read     Updated on 14 Aug 2026, 04:20 AM
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Tempest Therapeutics reported a Q2 2026 net loss of $5.2 million, down from $7.9 million YoY, driven by lower R&D expenses. Year-to-date losses widened to $32.9 million due to $22.1 million in acquired in-process R&D charges. The company advanced its CAR-T pipeline with a new partnership for TPST-4003 and positive interim data for TPST-2003, while cash reserves declined to $0.8 million.

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Tempest Therapeutics (NASDAQ: TPST) reported a second-quarter 2026 net loss of $5.2 million, or $(0.34) per share, narrowing significantly from the $7.9 million loss, or $(2.07) per share, recorded in the corresponding period of 2025. The company also provided updates on its clinical-stage pipeline, announcing a strategic partnership to advance its lead in vivo CAR-T candidate, TPST-4003, and reporting positive interim data for TPST-2003.

Financial Performance

The reduction in the quarterly net loss was driven by lower research and development (R&D) expenses, which fell to $1.8 million from $3.9 million in Q2 2025. This decrease resulted from the re-prioritization of efforts following an asset acquisition completed in February 2026. General and administrative (G&A) expenses also declined slightly to $3.4 million from $4.1 million year-over-year, primarily due to lower one-time separation costs compared to the prior year.

For the six months ended June 30, 2026, Tempest reported a net loss of $32.9 million, compared to $18.7 million in the same period of 2025. The year-to-date increase in losses was largely attributable to $22.1 million in acquired in-process R&D expenses related to the February 2026 asset acquisition, a non-recurring item not present in the prior year.

Metric Q2 2026 Q2 2025 H1 2026 H1 2025
Net Loss $5.2 million $7.9 million $32.9 million $18.7 million
Net Loss Per Share $(0.34) $(2.07) $(2.52) $(5.17)
R&D Expenses $1.8 million $3.9 million $1.9 million $11.5 million
G&A Expenses $3.4 million $4.1 million $8.9 million $7.4 million

Cash and cash equivalents decreased to $0.8 million as of June 30, 2026, from $7.7 million at the end of December 2025. The decline was offset partially by net proceeds of $1.7 million from a private placement and $1.7 million from a warrant inducement in the second quarter.

Pipeline and Corporate Updates

Tempest advanced its next-generation in vivo CAR-T platform with several key developments:

  • TPST-4003: The company unveiled its lead product candidate, a dual-targeting CD19/BCMA CAR-T therapy using CD7-targeted mRNA/LNP delivery. Tempest entered a strategic partnership with Hebei Senlang Biotechnology to develop this candidate, beginning with an investigator-initiated trial in China for approximately 10 patients with myasthenia gravis or multiple sclerosis. First patient dosing is anticipated in the fourth quarter of 2026.
  • TPST-2003: Positive interim results were reported for ongoing trials in relapsed/refractory multiple myeloma (rrMM) and POEMS syndrome. The therapy achieved a 100% complete response rate among 15 CAR-T-naïve efficacy evaluable patients across two trials, with no Grade ≥3 cytokine release syndrome or neurotoxicity observed in the rrMM trial. Additionally, Cincinnati Children’s AGCTC was selected as the lead contract development and manufacturing partner to support a potentially registrational study later this year.

On the corporate front, Tempest appointed Drake Richey and John Yee, MD, MPH, to its Board of Directors, and named Andrew Fang, Ph.D., as Head of Business Development to focus on global partnerships, particularly in China.

What the Numbers Show

The divergence between the quarterly and year-to-date financial results highlights the impact of non-recurring acquisition costs. While the Q2 operating performance improved with a narrower loss driven by reduced R&D spend, the H1 2026 net loss more than doubled year-over-year due to the $22.1 million charge for acquired in-process R&D. This suggests that the core operational burn rate has stabilized post-acquisition, but the balance sheet remains under pressure, evidenced by cash reserves dropping to $0.8 million, necessitating continued capital raising efforts as indicated by the recent warrant inducement and private placement.

Given the critically low cash balance of $0.8 million, what specific capital raising strategies or partnership milestones does Tempest need to achieve to ensure operational continuity through 2027?

How might the strategic partnership with Hebei Senlang Biotechnology for TPST-4003 impact Tempest's long-term revenue potential and regulatory pathway in the Chinese market?

What are the key risks associated with advancing TPST-2003 to a potentially registrational study, particularly regarding manufacturing scalability with the new CDMO partner?

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Tempest Therapeutics secures $50M equity purchase agreement with Lincoln Park

1 min read     Updated on 14 Aug 2026, 02:58 AM
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Tempest Therapeutics entered into a $50.0 million equity purchase agreement with Lincoln Park Capital on August 13, 2026. The deal allows for sales up to $25.0 million initially, with an automatic increase to the full amount subject to conditions. A registration statement must be filed with the SEC within 10 days.

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Tempest Therapeutics, Inc. has secured a capital infusion mechanism through a purchase agreement with Lincoln Park Capital Fund, LLC, committing to buy up to $50.0 million of the company’s common stock. The deal, executed on August 13, 2026, provides Tempest with flexible access to equity funding over a 24-month period, starting with an initial available amount of $25.0 million.

The agreement includes a registration rights agreement, ensuring that shares issued to Lincoln Park can be resold in the public market. Tempest has agreed to file a registration statement with the Securities and Exchange Commission (SEC) within 10 days of the execution date.

Deal Structure and Terms

The transaction is structured as an at-the-market offering, giving Tempest the right, but not the obligation, to sell shares at its sole discretion. Key terms include:

  • Total Commitment: Up to $50.0 million.
  • Initial Availability: $25.0 million.
  • Additional Amount: An automatic increase of $25.0 million, subject to limitations and satisfaction of conditions.
  • Duration: Up to 24 months from the Commencement Date.
  • Commencement Date: Defined as the date when all conditions, including the effectiveness of the SEC registration statement, are satisfied.
Term Detail
Counterparty Lincoln Park Capital Fund, LLC
Total Commitment $50.0 million
Initial Available Amount $25.0 million
Duration Up to 24 months
Stock Par Value $0.001 per share

Regulatory Filings

Tempest is obligated to file a registration statement under the Securities Act of 1933, as amended, no later than 10 days after executing the Purchase Agreement and Registration Rights Agreement. This filing is a prerequisite for the commencement of share sales, as it registers the resale of shares by Lincoln Park.

What the Numbers Show

The structure of the deal reveals a phased approach to capital raising. By setting the initial available amount at $25.0 million—exactly half of the total $50.0 million commitment—Tempest retains flexibility while securing a defined floor for potential proceeds. The automatic increase to the full amount suggests confidence in meeting the specified conditions, likely centered on regulatory approval and market stability, without requiring immediate renegotiation.

How might the potential dilution from issuing up to $50 million in new shares impact existing shareholders' equity value over the next 24 months?

What specific clinical or operational milestones is Tempest Therapeutics likely targeting with this capital infusion to justify the valuation and investor confidence?

Could the requirement to file an SEC registration statement within 10 days signal any underlying regulatory scrutiny or delays in Tempest's compliance history?

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