Tvardi Therapeutics (TVRD) Q1 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q1 2026 earnings summary
8 May, 2026Executive summary
Focused on developing oral STAT3 inhibitors for inflammatory and proliferative diseases, with lead candidates TTI-101 (in Phase 1b/2 for HCC) and TTI-109 (in Phase 1 for healthy volunteers); topline results for TTI-109 expected June 2026 and TTI-101 HCC data in 2H 2026.
Reported topline data from a Phase 2 trial in IPF for TTI-101 did not meet primary goals, but subset analysis showed promising exploratory biomarker reductions, including a 9.4% reduction in fibrosis score versus 2.4% for placebo and a 4.5-fold greater decline in IL-6 levels.
Merger with Cara Therapeutics completed in April 2025, resulting in a new public entity, recapitalization, and conversion of preferred stock and $28.3 million in convertible notes to common stock.
Interim findings from the REVERT LIVER CANCER trial demonstrated clinically meaningful activity for TTI-109, which is positioned as a next-generation STAT3 inhibitor with potential for improved tolerability and broader application.
Cash runway projected to fund operations through clinical readouts and into Q4 2026.
Financial highlights
Net loss for Q1 2026 was $6.8 million, a 29% improvement from $9.6 million in Q1 2025.
Operating expenses increased 62% year-over-year to $7.1 million, driven by higher R&D and G&A costs.
R&D expenses for Q1 2026 were $4.9 million, up from $3.1 million in Q1 2025, mainly due to higher TTI-109 development costs.
G&A expenses rose to $2.1 million from $1.2 million year-over-year, driven by higher personnel and professional fees.
Cash, cash equivalents, and short-term investments totaled $25.0 million as of March 31, 2026, down from $30.8 million at year-end 2025.
Outlook and guidance
Expects continued significant operating losses and negative cash flows as R&D investment continues.
Substantial doubt exists about ability to continue as a going concern without additional funding.
Plans to seek additional capital through equity, debt, or strategic partnerships; filed a $200 million shelf registration in May 2026.
Topline data for TTI-109 healthy volunteer study and clinical development strategy expected in June 2026; TTI-101 Phase 1b/2 HCC topline data anticipated in 2H 2026.
Current cash runway expected to support operations through clinical milestones and into Q4 2026.
Latest events from Tvardi Therapeutics
- Up to $200M in securities registered, including $12.5M ATM equity, to fund clinical pipeline.TVRD
Registration filing5 May 2026 - Annual meeting to elect directors, approve pay, and ratify auditor, with board support.TVRD
Proxy filing29 Apr 2026 - Annual meeting to vote on directors, executive pay, auditor, and key governance policies.TVRD
Proxy filing29 Apr 2026 - Net loss narrowed, cash runway extended, and key clinical milestones expected in 2026.TVRD
Q4 202531 Mar 2026 - All-stock merger forms a STAT3-focused biotech with key clinical milestones expected in 2025.TVRD
M&A Announcement10 Jan 2026 - Biotech developing oral STAT3 inhibitors for fibrosis and cancer faces high risk, no revenue, and urgent capital needs.TVRD
Registration Filing28 Nov 2025 - Reverse merger, $5.5M Q3 loss, $36.5M cash, and key 2026 clinical milestones ahead.TVRD
Q3 202513 Nov 2025 - Biotech developing oral STAT3 inhibitors for fibrosis and cancer, with no IPO proceeds to the company.TVRD
Registration Filing20 Oct 2025 - Q2 revenue fell 86% as NP program ended, staff cut 70%, and a strategic review began.TVRD
Q2 202413 Oct 2025