PYXS
Pyxis Oncology, Inc.4.0000
-0.2000-4.76%
Dec 16, 4:00:00 PM EST
Earnings Call Transcripts
This Quarter (Q4 '25)
No earnings call transcript available yet
Last Quarter (Q3 '25)
No earnings call transcript available
Key Stats
Market Cap
249.06MP/E (TTM)
-Basic EPS (TTM)
-1.58Dividend Yield
0%Recent Filings
8-K
10-Q
10-Q
Q2 FY2025 results
Pyxis Oncology posted Q2 revenue of $2.8M from a milestone on Suvemcitug approval in China, up from zero y/y, yet R&D costs climbed 23% y/y to $17.1M on micvotabart pelidotin trials while G&A dipped 11% y/y to $5.4M, yielding a $19.8M operating loss (derived) versus $20.0M last year. Net loss widened to $18.4M from $17.3M y/y, with EPS at -$0.30 on 61.9M shares, consistent with diluted weighting. Cash and equivalents fell to $10.7M from $19.5M at year-end, but $78.2M in short-term securities bolster liquidity to $88.9M total, funding operations into H2 2026 amid no debt. No M&A or non-GAAP metrics disclosed in the 10-Q. Competition from ADCs like those from Gilead and Pfizer threatens micvotabart pelidotin's edge in HNSCC.
8-K
Pyxis Q2 earnings and MICVO update
Pyxis Oncology reported Q2 2025 results, booking $2.8 million in milestone revenue from suvemcitug's China approval, while R&D expenses climbed to $17.1 million on MICVO trial advances. Cash stands at $90.4 million, funding operations into late 2026. MICVO monotherapy and KEYTRUDA combo studies in R/M HNSCC progress steadily. Preliminary data arrives second half 2025. Trials face inherent clinical risks.
8-K
Trial enrollment revisions posted
Pyxis Oncology updated patient enrollment caps for its Phase 1 monotherapy trial of micvotabart pelidotin (MICVO) on ClinicalTrials.gov on July 31, 2025, aligning with standard protocol practices for the first-in-human study in advanced solid tumors. The revisions set maximum participants without altering prior guidance on head and neck squamous cell carcinoma enrollment in the dose expansion phase. This ensures trial efficiency amid ongoing safety and efficacy assessments.
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