Nuvation Bio (NYSE:NUVB – Get Free Report) issued its quarterly earnings results on Monday. The company reported ($0.11) earnings per share for the quarter, meeting analysts’ consensus estimates of ($0.11), FiscalAI reports. Nuvation Bio had a negative net margin of 813.07% and a negative return on equity of 54.99%. The firm had revenue of $41.87 million for the quarter, compared to analyst estimates of $36.82 million.
Here are the key takeaways from Nuvation Bio’s conference call:
- IBTROZI secured full FDA approval (June 11, 2025) and the launch shows strong early adoption—432 new patients started in 2025 (216 in Q4) at a pace ~6x faster than the two prior ROS1 TKI launches.
- Management highlights an unusually durable clinical profile for IBTROZI—pooled median duration of response of ~50 months in TKI‑naive patients and an 89% confirmed ORR—attributing potential intracranial control to measured TRKB inhibition while preserving tolerability.
- Financial and corporate progress includes Q4 total revenue of $41.9M (including milestones), IBTROZI net U.S. product revenue of $15.7M in Q4 ($24.7M for 2025), approximately $529M in cash and marketable securities, and substantial ex‑U.S. partnerships (ASI/Eisai) that provide upfront proceeds and milestone/royalty upside.
- Near‑term revenue growth lagged patient starts because the early launch mix was heavily weighted to later‑line patients who discontinue quickly, and management expects gross‑to‑net (~25% now) to rise slightly, which may constrain short‑term sales momentum.
- Safusidenib advancement—global phase 3 SIGMA trial in high‑risk/high‑grade IDH1 mutant glioma is enrolling with a 2029 readout and a separate grade‑3 oligodendroglioma cohort expected in 2027 that could support accelerated approval discussions if ORR is compelling.
Nuvation Bio Stock Down 1.2%
Shares of NYSE NUVB opened at $5.84 on Tuesday. The firm’s 50-day moving average is $6.65 and its two-hundred day moving average is $5.53. The company has a market capitalization of $2.00 billion, a PE ratio of -9.13 and a beta of 1.51. Nuvation Bio has a 12-month low of $1.54 and a 12-month high of $9.75. The company has a debt-to-equity ratio of 0.14, a current ratio of 8.48 and a quick ratio of 8.39.
Analyst Upgrades and Downgrades
Check Out Our Latest Research Report on Nuvation Bio
Institutional Investors Weigh In On Nuvation Bio
Institutional investors and hedge funds have recently bought and sold shares of the stock. Man Group plc acquired a new position in shares of Nuvation Bio in the 2nd quarter valued at about $75,000. Kestra Advisory Services LLC purchased a new position in Nuvation Bio in the fourth quarter valued at approximately $71,000. Mackenzie Financial Corp lifted its position in Nuvation Bio by 38.8% during the third quarter. Mackenzie Financial Corp now owns 15,746 shares of the company’s stock valued at $58,000 after buying an additional 4,400 shares in the last quarter. Prudential Financial Inc. grew its stake in Nuvation Bio by 112.3% during the second quarter. Prudential Financial Inc. now owns 28,905 shares of the company’s stock worth $56,000 after buying an additional 15,290 shares during the period. Finally, BNP Paribas Financial Markets grew its stake in Nuvation Bio by 113.9% during the second quarter. BNP Paribas Financial Markets now owns 28,152 shares of the company’s stock worth $55,000 after buying an additional 14,989 shares during the period. Hedge funds and other institutional investors own 61.67% of the company’s stock.
Nuvation Bio Company Profile
Nuvation Bio is a clinical-stage biotechnology company dedicated to discovering and developing small-molecule therapies for patients with cancer. The company employs an integrated research and development platform that spans target identification, preclinical evaluation, process chemistry, and early-stage clinical trials. By centralizing these capabilities, Nuvation Bio aims to accelerate the translation of promising drug candidates from laboratory research to first-in-human studies.
The company’s pipeline comprises multiple oncology programs, with small-molecule kinase inhibitors and targeted agents in Phase 1 development for both hematologic malignancies and solid tumors.
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