APVO
Aptevo Therapeutics Inc.1.1000
+0.0600+5.77%
Dec 16, 4:00:01 PM EST
Earnings Call Transcripts
This Quarter (Q1 '26)
No earnings call transcript available yet
Last Quarter (Q4 '25)
No earnings call transcript available
Key Stats
Market Cap
18.54MP/E (TTM)
0.00Basic EPS (TTM)
1950.74Dividend Yield
0%Recent Filings
8-K
Mipletamig AML data shines
Aptevo unveiled preliminary Phase 1b/2 RAINIER trial data at ASH 2025, showing mipletamig plus AZA/VEN delivered 93% ORR and 87% CR/CRi in frontline AML patients unfit for intensive chemo, with 100% CRS-free. Median age 75; 43% had poor-prognosis TP53 mutations. No CRS sets it apart. Trial enrollment continues.
8-K
89% AML remission, trispecifics launched
Aptevo Therapeutics reported Q3 2025 results, highlighting 89% remission among evaluable frontline AML patients on mipletamig combo therapy across two trials—no CRS observed. It unveiled trispecifics APVO451 and APVO452 for solid tumors, expanding its CD3 portfolio to five. Cash hit $21.1M after $18.7M raised; runway extends into 4Q26. Net loss widened to $7.5M.
10-Q
Q3 FY2025 results
Aptevo's Q3 losses widened to $7.6M from $5.2M y/y (derived), driven by R&D up 30% to $4.0M on mipletamig acceleration and G&A up 69% to $3.6M from higher employee costs; net loss hit $7.5M while a $1.5M warrant down-round dividend pushed common loss to $9.0M. Cash swelled to $21.1M on $32.7M equity raises via SEPA/ATM, funding ops into 4Q26. Operating cash burn was $20.4M YTD, up from $18.0M. Shares exploded post-reverse split. Dilution fuels the burn.
8-K
Rights plan extended one year
Aptevo Therapeutics extended its shareholder rights plan by one year, pushing the final expiration date to October 29, 2026, via Amendment No. 5 signed on October 30, 2025. This tweak to the 2020 Rights Agreement, which issues preferred stock rights against hostile takeovers, bolsters defenses amid biotech volatility. Yet the board eyes stability. No financial impacts disclosed.
8-K
100% remission in AML trial cohort
Aptevo Therapeutics announced a 100% remission rate in Cohort 3 of its Phase 1b/2 RAINIER trial, testing mipletamig with venetoclax and azacitidine in newly diagnosed AML patients unfit for intensive chemotherapy. No dose-limiting toxicities or cytokine release syndrome emerged across cohorts, highlighting mipletamig's clean safety profile. This bolsters mipletamig's frontline potential in a multibillion-dollar AML market. Cohort 4 enrollment is underway.
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