SCYNEXIS(US:SCYX) Globenewswire·2025-05-15 20:20Core Insights - SCYNEXIS, Inc. reported its financial results for Q1 2025, highlighting significant developments in its clinical programs and financial performance [1][6]. Clinical Developments - The FDA lifted the clinical hold on ibrexafungerp, allowing the Phase 3 MARIO study to resume, which evaluates ibrexafungerp for invasive candidiasis treatment [4][7]. - SCYNEXIS is addressing a disagreement with GSK regarding the termination of the MARIO study, asserting that GSK does not have the right to unilaterally terminate it under their license agreement [4][7]. - The company is also advancing its second-generation fungicide candidate, SCY-247, with Phase 1 study results expected in Q3 2025 [2][8]. Financial Performance - For Q1 2025, SCYNEXIS reported license agreement revenue of $0.3 million, a decrease from $1.4 million in Q1 2024 [9]. - Research and development expenses decreased to $5.1 million in Q1 2025 from $7.2 million in Q1 2024, a reduction of 29% [10]. - The net loss for Q1 2025 was $5.4 million, or $(0.11) per share, compared to a net income of $0.4 million, or $0.01 per share, in Q1 2024 [13]. Cash Position - As of March 31, 2025, SCYNEXIS had cash, cash equivalents, and investments totaling $53.8 million, down from $75.1 million at the end of 2024 [14][20]. - The company projects a cash runway into Q3 2026 based on its current operating plan [14][17]. Market Context - SCYNEXIS is focused on developing antifungal solutions to combat the rising threat of drug-resistant fungal infections, particularly invasive candidiasis, which has limited treatment options [3][15]. - The company’s first antifungal agent, ibrexafungerp, is already approved in the U.S. for vulvovaginal candidiasis and is in late-stage development for other indications [15][16].