Loading...
Access earnings results, analyst expectations, report, slides, earnings call, and transcript.
The earnings report shows strong financial performance, with record high gross margins and a new partnership with J&J MedTech, enhancing growth prospects. Despite some declines in specific product sales, the overall outlook remains optimistic with raised guidance and shareholder-friendly actions like stock repurchase. The Q&A revealed some management evasiveness, but the positive aspects outweigh these concerns, suggesting a positive stock price movement.
EXPAREL sales $142.9 million in Q2 2025, up from $136.9 million in Q2 2024, representing a 4% growth. This growth was driven by a 6% increase in volume, partially offset by a shift in vial mix and discounting.
ZILRETTA sales $31.3 million in Q2 2025, up from $30.7 million in Q2 2024, showing a slight increase. The growth is attributed to the new partnership with J&J MedTech and other programs.
iovera° sales $5.6 million in Q2 2025, slightly down from $5.7 million in Q2 2024. No specific reasons for the decline were mentioned.
Non-GAAP gross margin Improved to 82% in Q2 2025 from 76% in Q2 2024. This improvement was due to enhanced manufacturing efficiencies and the use of large-scale manufacturing suites.
Non-GAAP R&D expense $24.7 million in Q2 2025, up from $18.4 million in Q2 2024. The increase is related to strong enrollment in the Phase II study of PCRX-201 and expenses associated with ZILRETTA and iovera° registrational studies.
Non-GAAP SG&A expense $77.2 million in Q2 2025, up from $59 million in Q2 2024. The increase is due to investments in commercial, medical, and market access organizations, targeted marketing initiatives, and field force expansion.
Adjusted EBITDA $54.3 million in Q2 2025. This reflects significant operating cash flow, but no year-over-year comparison or reasons for change were provided.
EXPAREL: Achieved 6% year-over-year volume growth, the highest in 8 quarters. Enhanced market opportunity due to CMS policy changes for outpatient settings. Expanded commercial coverage to over 40 million lives, aiming for 60 million by year-end.
ZILRETTA: Entered a transformative collaboration with Johnson & Johnson MedTech, doubling sales calls and expanding reach to various physician specialists. Sales increased to $31.3 million in Q2 2025 from $30.7 million in 2024.
PCRX-201: Presented 3-year follow-up data showing sustained efficacy and tolerability. Phase II ASCEND study enrollment on track to conclude by year-end.
Market Access for EXPAREL: Expanded commercial coverage to over 40 million lives, targeting 60 million by year-end. Focused on key markets with high procedural volumes, particularly in top 5 states accounting for 40% of EXPAREL volumes.
Strategic Partnerships: Formed a collaboration with Johnson & Johnson MedTech for ZILRETTA, significantly expanding market reach and patient access.
Manufacturing Efficiencies: Improved gross margins to 82% in Q2 2025 from 76% in 2024 due to enhanced manufacturing efficiencies and decommissioning of older facilities.
Capital Allocation: Repurchased $50 million in common stock and reduced debt with a new $300 million revolving credit facility.
5x30 Strategy: Focused on achieving 5 partnerships by 2030 and advancing leadership in musculoskeletal pain treatments.
Pipeline Development: Progressed registrational studies for ZILRETTA and iovera° and advanced the PCRX-201 Phase II ASCEND study.
Regulatory Changes: CMS's proposed policy to phase out the inpatient-only list and add procedures to ambulatory surgical centers could impact the market dynamics for EXPAREL, requiring adaptation to new reimbursement structures.
Patent Challenges: The reexamination and amendment of the 495 patent claims indicate ongoing legal and intellectual property risks, which could affect product exclusivity and market position.
Competitive Pressures: The collaboration with J&J MedTech for ZILRETTA highlights the need to address competitive pressures in the OA pain solutions market, requiring effective execution to leverage the partnership.
Manufacturing Adjustments: Decommissioning the 45-liter suite and optimizing workforce could pose short-term operational risks during the transition to larger-scale manufacturing suites.
Market Adoption: Broader market adoption of EXPAREL is expected to take time, with some facilities indicating a 6-12 month timeline for implementing CMS reimbursement guidelines, potentially delaying revenue growth.
Economic Pressures: Discounting and vial mix shifts have partially offset sales growth, indicating pricing pressures that could impact profitability.
R&D and Pipeline Risks: Increased R&D expenses for pipeline advancements, such as PCRX-201 and ZILRETTA studies, represent financial risks if these initiatives do not yield expected results.
Revenue Guidance: The company has narrowed its full-year revenue guidance range to $730 million to $750 million for 2025.
Gross Margin Guidance: The company has increased its full-year non-GAAP gross margin guidance to 78%-80%, up from the previous range of 76%-78%, driven by manufacturing efficiencies and favorable production volumes.
EXPAREL Market Opportunity: CMS is proposing to phase out the inpatient-only list over the next three years, starting in 2026, which is expected to enhance the market opportunity for EXPAREL in outpatient settings.
EXPAREL Utilization Growth: The company expects EXPAREL utilization to grow steadily, with a target of reaching 60 million covered commercial lives by the end of 2025 and a total covered population of nearly 100 million lives across commercial and government payers.
ZILRETTA Growth: The partnership with Johnson & Johnson MedTech is expected to significantly accelerate ZILRETTA's growth trajectory by doubling sales calls and expanding patient access.
Pipeline Development: The company is advancing its Phase II ASCEND study for PCRX-201, with enrollment in Part A expected to conclude by year-end 2025. It is also progressing registrational studies for ZILRETTA in shoulder OA and iovera° in spasticity.
Capital Allocation: The company plans to continue opportunistic stock repurchases, with $250 million remaining under its current buyback authorization through 2026.
Share Repurchase: During the second quarter, the company executed $50 million in share repurchases, retiring approximately 2 million shares of common stock. This is in addition to the $25 million repurchase executed last year. The company has approximately $250 million remaining under its current buyback authorization, which runs through the end of 2026. The company plans to continue being opportunistic with stock repurchases.
The earnings call shows strong financial performance with growth in sales and improved margins. The company's strategic partnerships, especially with J&J, are poised to boost future growth. The market opportunity for EXPAREL and positive feedback on the pipeline reinforce optimism. Share repurchases signal confidence in undervaluation. Despite some unclear management responses, overall guidance and strategic initiatives support a positive sentiment.
The earnings report shows strong financial performance, with record high gross margins and a new partnership with J&J MedTech, enhancing growth prospects. Despite some declines in specific product sales, the overall outlook remains optimistic with raised guidance and shareholder-friendly actions like stock repurchase. The Q&A revealed some management evasiveness, but the positive aspects outweigh these concerns, suggesting a positive stock price movement.
The earnings call indicates strong financial performance with increased EXPAREL sales and improved gross margins. The stock repurchase program signals confidence in future growth, while guidance aligns with strategic goals. Despite concerns in the Q&A about adoption and competition, the optimistic guidance and strategic initiatives suggest a positive outlook. The positive impact of financial metrics and shareholder returns outweighs the uncertainties, leading to a predicted stock price increase of 2% to 8% over the next two weeks.
All transcripts are sourced directly from the official live webcast or the company’s official investor relations website. We use the exact words spoken during the call with no paraphrasing of the core discussion.
Full verbatim transcripts are typically published within 4–12 hours after the call ends. Same-day availability is guaranteed for all S&P 500 and most mid-cap companies.
No material content is ever changed or summarized in the “Full Transcript” section. We only correct obvious spoken typos (e.g., “um”, “ah”, repeated 10 times”, or clear misspoken ticker symbols) and add speaker names/titles for readability. Every substantive sentence remains 100% as spoken.
When audio quality is poor or multiple speakers talk over each other, we mark the section instead of guessing. This ensures complete accuracy rather than introducing potential errors.
They are generated by a specialized financial-language model trained exclusively on 15+ years of earnings transcripts. The model extracts financial figures, guidance, and tone with 97%+ accuracy and is regularly validated against human analysts. The full raw transcript always remains available for verification.