StockWatch
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Keros Therapeutics, Inc. Q3 FY26 Results

KROSQ3 FY26 Results
Filing
MetricValue ($ M)Q3 FY25
Revenue40.01180.6%
Total Income40.01180.6%
Expenditure27.198.3%
PBT14.93271.6%
Net Profit14.15294.4%
OPM32.04%
NPM35.38%86.42pp
EPS0.71494.4%
View full financials

Keros Therapeutics Reports Q3 2026 Financial Results and Business Highlights

06 Nov 2026 · 13h ago

Summary

Keros Therapeutics reported a net income of $14.2 million for the third quarter of 2026, a substantial improvement from a net loss of $7.3 million in the prior year's quarter, largely due to license revenue from Takeda. Total revenue for the quarter reached $40.0 million. The company also provided updates on its pipeline, including the dosing of the first patient in a Phase 2 trial for Duchenne muscular dystrophy and the nomination of a new preclinical asset, KER-206. Keros anticipates its current cash position will support operations into the second half of 2028.

Key Highlights

  1. 1

    Keros Therapeutics reported net income of $14.2 million for the third quarter of 2026, a significant increase from a net loss of $7.3 million in the third quarter of 2025.

  2. 2

    Total revenue for the third quarter of 2026 was $40.0 million, primarily driven by license revenue recognized from the agreement with Takeda.

  3. 3

    Research and development expenses for Q3 2026 were $20.5 million, an increase from $19.5 million in Q3 2025, supporting pipeline advancement.

  4. 4

    General and administrative expenses decreased to $6.7 million in Q3 2026 from $10.1 million in Q3 2025.

  5. 5

    The company expects its cash and cash equivalents to fund operations into the second half of 2028.

  6. 6

    The first patient was dosed in the Phase 2 clinical trial of rinvatercept for Duchenne muscular dystrophy in September 2026.

  7. 7

    A novel ligand trap, KER-206, was nominated from the nonclinical pipeline for further investigation.

Management Comments

J

Jasbir S. Seehra

We are excited to continue advancing our pipeline across both clinical and nonclinical development, building on our understanding of TGF-β biology to develop potential new treatments for patients. We remain focused on disciplined execution of our strategic priorities as we work to advance our programs and build on the potential of our pipeline.

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