10-Q · May 11, 2026
SCYNEXIS, Inc. reported a significant increase in net loss to $21.3 million for Q1 2026, compared to a net loss of $5.4 million in Q1 2025, largely driven by increased research and development costs. The company…
Earnings analysis · 10-Q
Filed August 10, 2026 · Our reading of the company's report
The latest report
SCYNEXIS reported a Q2 2026 accounting profit of $7.397 million, or $0.63 diluted EPS, versus a $6.885 million loss in the prior-year quarter, but the result was driven primarily by a $14.152 million noncash…
SCYNEXIS reported a Q2 2026 accounting profit of $7.397 million, or $0.63 diluted EPS, versus a $6.885 million loss in the prior-year quarter, but the result was driven primarily by a $14.152 million noncash warrant-liability gain. Revenue declined to $235,000 from $1.364 million, while six-month operating losses widened to $24.715 million and operating cash use increased to $22.986 million. The March private placement improved liquidity to $71.1 million of cash and investments and management expects funding into 2029, supporting planned SCY-770 milestones, although substantial future financing and clinical-development risks remain.
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Q2 2026 net income was $7.397 million, or $0.63 diluted EPS, versus a $6.885 million net loss, or $(1.11) diluted EPS, in Q2 2025. The improvement was driven primarily by a $14.152 million warrant-liability fair-value gain, which was largely noncash.
Cash, cash equivalents and investments totaled $71.1 million at June 30, 2026 versus $56.3 million at December 31, 2025. Management stated that these resources are expected to fund ongoing operations into 2029.
The March 2026 private placement generated $40.0 million of gross proceeds and $36.9 million of net proceeds. The company may receive up to an additional $52.2 million in gross proceeds if the warrants are fully exercised for cash.
Q2 research and development expense fell 45.5% year over year to $3.891 million from $7.141 million, primarily due to lower CMC, preclinical and legacy MARIO Phase 3 costs. Six-month R&D expense nevertheless rose 32.3% to $16.243 million because of the $8.0 million SCY-770 acquired IPR&D charge.
Management anticipates completing the SCY-770 Phase 1 confirmatory study in Q3 2026 and initiating a Phase 2 ADPKD proof-of-concept study in Q4 2026. An early efficacy readout is expected in the second half of 2027.
The company regained Nasdaq minimum-bid compliance after its closing bid price was at least $1.00 for 10 consecutive business days from June 1 through June 12, 2026. The matter was closed on June 15, 2026.
Operating cash outflow was $22.986 million in the six months ended June 30, 2026, up from $14.960 million in the prior-year period. Management states that substantial additional funding will be required and that capital needs could exceed current estimates.
The March 2026 financing increased common shares outstanding to 9,949,609 at June 30, 2026 from 5,442,688 at December 31, 2025. The transaction also added warrants for 5,437,464 shares and pre-funded warrants for 1,093,744 shares, creating substantial potential dilution.
Revenue was only $235,000 in Q2 2026, down from $1.364 million in Q2 2025, and consists of license agreement revenue associated with GSK. The company therefore remains dependent on licensing economics and future milestones rather than recurring product sales.
Six-month net loss widened to $13.902 million from $12.276 million despite the Q2 profit. The six-month operating loss increased to $24.715 million from $18.190 million, reflecting continued substantial development and corporate expenses.
SCY-770 requires additional clinical development, including a planned Phase 2 study in Q4 2026, while SCY-247 Phase 2 development is subject to Phase 1 results and available funding. The company has not established that either program will achieve clinical or regulatory success.
The company recorded an accumulated deficit of $399.0 million at June 30, 2026 and stated that liquidity could be materially affected by negative regulatory events, unanticipated development costs, strategic-alliance costs or an inability to raise additional capital.
No quantitative revenue or EPS guidance was provided. Management expects cash and cash equivalents and investments of $71.1 million at June 30, 2026 to fund ongoing operations into 2029. Management anticipates completing the SCY-770 Phase 1 confirmatory study in Q3 2026, initiating a Phase 2 proof-of-concept study in Q4 2026, and obtaining an early efficacy readout in the second half of 2027. SCY-247 Phase 1 IV data are anticipated in Q3 2026, with a potential Phase 2 study in the first half of 2027 subject to results and funding.
SCYNEXIS, Inc. reported a significant increase in net loss to $21.3 million for Q1 2026, compared to a net loss of $5.4 million in Q1 2025, largely driven by increased research and development costs. The company…
SCYNEXIS reported a Q4 2025 revenue surge (Q4 revenue $18,646,000) and GAAP diluted EPS of $0.25 driven by one-time, non‑refundable payments from GSK totaling $24.8 million (Binding 2025 MOU). Operationally the company…
SCYNEXIS reported Q2 2025 license agreement revenue of $1,364,000 (up $628,000 or +85% vs Q2 2024 $736,000) and a narrower loss per share of $(0.14) vs $(0.30) in Q2 2024. Operating loss remained sizable at $(9,561,000)…
SCYNEXIS reported license agreement revenue of $257 (thousands) and GAAP net loss of $(5,391) (thousands), or $(0.11) per share, for Q1 2025 versus license revenue of $1,373 (thousands) and net income of $411…
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