Pliant Therapeutics experienced a net loss of $49.7 million in the fourth quarter of 2024, an increase from the prior-year quarter, mainly driven by higher research and development costs associated with the BEACON-IPF Phase 2b/3 clinical trial, which was discontinued following DSMB recommendation.
BEACON-IPF Phase 2b trial was discontinued due to an imbalance in unadjudicated IPF-related adverse events, despite early signs of efficacy on FVC.
Research and development expenses increased to $38.8 million, up from $33.2 million in the prior-year quarter, primarily due to the BEACON-IPF trial.
General and administrative expenses rose to $14.5 million, from $13.9 million, due to increased employee-related expenses.
The company reported a net loss of $49.7 million, compared to $41.1 million in the prior-year quarter.
Pliant Therapeutics expects its current cash, cash equivalents, restricted cash, and short-term investments to be sufficient to fund operations for the next 12 months and beyond.