24/7 Market News Snapshot 13 February, 2025 – Pliant Therapeutics, Inc. Common Stock (NASDAQ:PLRX)

DENVER, Colo., 13 February, 2025 (247marketnews.com) – (NASDAQ:PLRX) are discussed in this article.
Pliant Therapeutics, Inc. (PLRX) is experiencing a notable bullish trend, with shares trading at $3.107 in the pre-market, reflecting a 14.23% increase over the last closing value of $2.720. This surge is accompanied by robust trading activity, with a volume of approximately 1.32 million shares exchanged, indicating heightened investor interest. Analysts suggest that if PLRX can sustain this upward movement and surpass crucial resistance levels, it may attract further buying interest, potentially leading to additional gains. Traders are advised to remain vigilant for any pullbacks at support levels to identify favorable buying opportunities. The technical indicators currently suggest a positive outlook for PLRX in the near term.

In tandem with its promising market performance, Pliant Therapeutics is advancing its clinical endeavors with the BEACON-IPF Phase 2b trial, which evaluates the investigational treatment bexotegrast for idiopathic pulmonary fibrosis (IPF). The company has established an expert panel at the recommendation of the independent Data Safety Monitoring Board (DSMB) to conduct an unblinded review of key trial data. This panel consists of distinguished specialists in pulmonary diseases and biostatistics who will assess the efficacy and safety data to guide potential enrollment resumption.

The panel’s assessment is anticipated to be completed within two to four weeks, following which their insights will be provided to the DSMB to determine the next steps for the trial. Prior to this development, Pliant had paused patient enrollment to perform a thorough analysis to maintain the study’s integrity. The ongoing efforts underline Pliant’s commitment to pioneering therapeutic advancements for fibrotic diseases, with bexotegrast positioned as a critical component of its portfolio, recently acknowledged for its potential by both the FDA and EMA.

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