Welcome to our dedicated page for Cvs Health SEC filings (Ticker: CVS), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
CVS Health’s integrated model—retail pharmacies, a leading PBM and a major insurer—produces sprawling SEC documents that mix drug-pricing mechanics with insurance risk metrics. Finding where opioid litigation reserves sit in a 10-K or tracking when executives sell shares before material announcements can feel impossible.
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CVS Health’s Q2-25 10-Q shows top-line strength but margin pressure. Total revenue rose 8.4% YoY to $98.9 bn on higher pharmacy volumes (+9% Pharmacy & Consumer Wellness) and PBM growth (+10% Health Services). Six-month revenue is up 7.7% to $193.5 bn.
Profitability weakened. Q2 operating income fell 22% to $2.38 bn and net income attributable to CVS dropped 42% to $1.02 bn; diluted EPS slid to $0.80 (vs $1.41). For the first half, EPS declined 3% to $2.21, reflecting cost inflation, $448 mn premium deficiency on individual exchange products (recorded Q1) and an additional $471 mn reserve for Group Medicare Advantage in Q2. The Health Services unit also booked $288 mn of losses tied to exiting ACO REACH and selling its MSSP operations (including a $236 mn loss on divestiture).
Cash & balance sheet. Operating cash flow fell to $6.45 bn (-19% YoY). Cash & equivalents climbed to $11.8 bn (from $8.6 bn) aided by lower CapEx and debt repayments ($0.8 bn repaid; no new long-term debt issued). Net debt fell ~2 %, while equity rose to $77.4 bn. No share buybacks YTD; dividends of $0.665 per share continue.
Management confirms four-segment structure and notes planned exit from ACA individual exchanges by Jan-26. 1.268 bn shares were outstanding at 7/23/25.
COMPASS Pathways plc (Nasdaq: CMPS) filed its Q2-25 Form 10-Q. The clinical-stage biotech remains pre-revenue and focuses on COMP360 psilocybin for treatment-resistant depression (TRD) and post-traumatic stress disorder (PTSD).
- Phase 3 progress: Trial COMP005 (n=258) hit its primary MADRS endpoint (p<0.001; −3.6 vs placebo) with top-line 6-week data; 26-week read-outs will follow COMP006 Part A completion (H2-26).
- Operating results: Q2 net loss widened slightly to $38.4 m (-$0.41/sh) versus $38.1 m prior-year; six-month loss narrowed to $56.3 m from $73.3 m as G&A fell 12% and R&D rose 13%.
- Cash position: Cash & equivalents rose to $221.9 m (31 Dec-24: $165.1 m) after a $149.8 m January equity/warrant financing and $140.5 m H1 financing cash inflow. Management projects runway into 2027.
- Balance sheet: Warrant liabilities introduced at $74.4 m; total debt $31.0 m under Hercules loan (14.8% EIR) with $22.5 m minimum-cash covenant. Share count expanded to 95.9 m ADS equivalents.
- Cash flow: H1 operating cash burn $84.3 m offset by $140.5 m financing inflow; cap-ex immaterial.
Outlook: Key near-term catalysts are FDA dialogue on COMP005 data and continued enrollment of COMP006. Management is designing a late-stage PTSD program. Despite ample cash, future dilution risk persists via 35.1 m outstanding pre-funded & 2025 ADS warrants and $122 m of PIPE warrants.