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ANGO Stock Down Despite Q4 Earnings Beat, Gross Margin Declines
ZACKS· 2025-07-16 17:36
Key Takeaways ANGO posted Q4 FY25 revenues of $80.2 million, up 12.9% and ahead of the consensus mark by 7.5%. Adjusted Q4 loss per share of 3 cents narrowed from 6 cents and beat the consensus mark of 13 cents. Gross margin fell 161 bps to 52.7% despite 9.4% growth in pro forma gross profit.AngioDynamics, Inc. (ANGO) reported an adjusted loss per share of 3 cents for fourth-quarter fiscal 2025, narrower than the year-ago quarter’s adjusted loss per share of 6 cents and the Zacks Consensus Estimate of a l ...
JNJ Begins Drug Sector Q2 Earnings With a Beat & Guidance Raise
ZACKS· 2025-07-16 15:55
Core Insights - Johnson & Johnson (JNJ) reported second-quarter 2025 earnings of $2.77 per share, exceeding the Zacks Consensus Estimate of $2.66, but reflecting a 1.8% decline year over year [1] - Total sales reached $23.74 billion, surpassing the Zacks Consensus Estimate of $22.80 billion, with a year-over-year increase of 5.8% [2] - The company raised its 2025 sales forecast to a range of $93.2 billion to $93.4 billion, indicating a growth of 5.1% to 5.6% compared to previous expectations [18][19] Financial Performance - Adjusted earnings, excluding intangible amortization and special items, were reported at $2.77 per share, while reported earnings, including these items, were $2.29 per share, up 18.7% year over year [1] - Domestic sales increased by 7.8% to $13.54 billion, while international sales rose by 3.2% to $10.2 billion [3] Segment Performance - The Innovative Medicines segment saw sales rise by 4.9% year over year to $15.2 billion, driven by strong performances from key products like Darzalex and Erleada [5][6] - The MedTech segment reported sales of $8.54 billion, up 7.3% from the previous year, benefiting from operational growth and currency impacts [16] Product Highlights - Darzalex sales increased by 23.0% to $3.54 billion, outperforming estimates [7] - Stelara sales declined by 42.7% to $1.65 billion due to biosimilar competition [11][12] - New drugs such as Carvykti and Tecvayli contributed significantly to sales growth, with Carvykti recording $439 million in sales [10] Future Outlook - JNJ anticipates operational sales growth in both the Innovative Medicine and MedTech segments to be higher in the second half of 2025 [25] - The company considers 2025 a "catalyst year" for growth, despite challenges such as the Stelara patent cliff and ongoing legal issues [26]
Abbott Earnings Are Imminent; These Most Accurate Analysts Revise Forecasts Ahead Of Earnings Call
Benzinga· 2025-07-16 15:43
Core Insights - Abbott Laboratories is set to release its second-quarter earnings results on July 17, with expected earnings of $1.25 per share, an increase from $1.14 per share in the same period last year [1] - The company anticipates quarterly revenue of $11.02 billion, up from $10.38 billion a year earlier [1] - Abbott received FDA approval for its Tendyne™ transcatheter mitral valve replacement system, which positively impacted its stock price [2] Analyst Ratings - Morgan Stanley analyst David Lewis maintained an Equal-Weight rating and raised the price target from $127 to $137 [5] - Raymond James analyst Jayson Bedford maintained an Outperform rating and increased the price target from $132 to $142 [5] - Barclays analyst Matt Miksic maintained an Overweight rating and slightly raised the price target from $158 to $159 [5] - Stifel analyst Rick Wise maintained a Buy rating and increased the price target from $135 to $145 [5] - Jefferies analyst Matthew Taylor maintained a Hold rating and raised the price target from $135 to $137 [5]
GMED Unveils Next-Gen Oscillating System DuraPro: Stock to Gain?
ZACKS· 2025-07-16 14:05
Company Developments - Globus Medical, Inc. (GMED) has launched DuraPro, a next-generation oscillating system with Excelsius navigation capabilities, aimed at enhancing procedural workflows through improved safety and efficiency [1][8] - The company has introduced 18 new products in 2024, including the ExcelsiusHub and ExcelsiusFlex surgical navigation systems, and expanded its Advanced Materials Science implant portfolio with the COHERE ALIF Spacer in Q1 2025 [3] - The DuraPro system features advanced oscillating technology that prevents soft tissue wrapping and allows for accurate bone removal while protecting delicate tissue [5][8] - GMED has also launched Verzera, a navigated high-speed drill system that integrates with ExcelsiusGPS and ExcelsiusHub, enhancing surgical workflows [6] Financial Performance and Market Outlook - GMED has a market capitalization of $7.56 billion, with 2025 revenue expected to rise by 12.8% year over year according to the Zacks Consensus Estimate [4] - The company has delivered an average earnings surprise of 10.1% over the trailing four quarters [4] - Despite recent product launches, GMED shares have declined by 23.2% over the past year, compared to a 13.7% decline in the industry [11] Industry Trends - The global high-speed surgical drill market is projected to grow from $2.44 billion in 2025 at a compound annual growth rate of 7.8% from 2025 to 2033, driven by the rise in minimally invasive surgical procedures and technological advancements [9]
Hologic Rides on AI-Powered Breast Health Innovations: What's Next?
ZACKS· 2025-07-16 13:55
Key Takeaways HOLX leads in mammography with AI-powered tools like Genius 3D and Genius Detection 2.0. Hologic's Genius Detection PRO promises fewer false positives and earned a top innovation award. HOLX plans to launch Envision, the fastest 3D mammography platform with a 2.5-second scan.Breast cancer continues to be a significant global health challenge and the leading cause of cancer-related deaths among women. Artificial Intelligence is playing an increasingly vital role in addressing this issue, whic ...
J&J(JNJ) - 2025 Q2 - Earnings Call Transcript
2025-07-16 13:30
Financial Data and Key Metrics Changes - In Q2 2025, worldwide sales reached $23.7 billion, reflecting a 4.6% increase despite a headwind from Stellara [23][24] - Net earnings for the quarter were $5.5 billion, with diluted earnings per share of $2.29, compared to $1.93 a year ago [24] - Adjusted net earnings were $6.7 billion, with adjusted diluted earnings per share of $2.77, representing a decrease of 2.1% year-over-year [25][32] Business Line Data and Key Metrics Changes - Innovative Medicine reported worldwide sales of $15.2 billion, increasing by 3.8% despite an 11.7% headwind from Stellara [25][26] - MedTech achieved worldwide sales of $8.5 billion, growing by 6.1%, with strong performance in cardiovascular, surgery, and vision [29][30] - In oncology, DARZALEX grew by 21.5%, while CARVICTI saw over 100% growth [26][27] - Tremfya in immunology grew by 30.1%, while Stellara declined by 43.2% due to biosimilar competition [28] Market Data and Key Metrics Changes - U.S. sales growth was 7.6%, while international sales saw a decline of 1.6% due to Stellara biosimilars and COVID-19 vaccine impacts [25][26] - Cardiovascular segment delivered over 22% operational sales growth, driven by new product performance [17][29] - Surgical vision grew by 8.9%, supported by strong performance in contact lenses and intraocular lenses [21][30] Company Strategy and Development Direction - The company aims to become the number one oncology company by 2030, targeting over $50 billion in sales [10][11] - Focus areas for growth include oncology, immunology, neuroscience, cardiovascular, surgery, and vision, with a commitment to innovation [8][12] - The company plans to launch several new products and expand its pipeline, including TAR200 for bladder cancer and icotrokinra for psoriasis [47][48] Management's Comments on Operating Environment and Future Outlook - Management expressed confidence in achieving and potentially exceeding growth targets for 2025, driven by strong performance in both Innovative Medicine and MedTech [36][39] - The company anticipates an acceleration in operational sales growth in the second half of the year, supported by new product launches and market share gains [40][46] - Management highlighted the importance of navigating external challenges, including tariffs and competition, while maintaining a focus on innovation and market leadership [88] Other Important Information - The company ended Q2 with $19 billion in cash and marketable securities and $51 billion in debt, resulting in a net debt position of $32 billion [38] - The effective tax rate for the quarter was 14.7%, down from 18.5% in the previous year [33] - The company is committed to investing $55 billion in the U.S. over the next four years, driven by favorable tax policies [39] Q&A Session Summary Question: Drivers of upside to guidance for the year - Management indicated that both Innovative Medicine and MedTech contributed to strong performance, with notable growth in oncology and cardiovascular segments [52][53] Question: Oncology target of $50 billion by the end of the decade - Management expressed confidence in achieving this target, citing strong growth in multiple myeloma and the potential of TAR200 for bladder cancer [68][71] Question: Guidance for operational growth and operating margin improvement - Management expects 2026 to show better growth rates than 2025, with ongoing efforts to improve operating margins [81][83] Question: Impact of pharma tariffs and manufacturing capacity - Management acknowledged uncertainty regarding tariffs but emphasized ongoing investments in U.S. manufacturing and job creation [88]
Intuitive demonstrates telesurgery capabilities
Globenewswire· 2025-07-16 13:16
Core Viewpoint - Intuitive has successfully demonstrated its telesurgery capabilities by connecting two surgeons remotely to perform a transatlantic surgery at the Society of Robotic Surgery conference, showcasing advancements in robotic-assisted surgery technology [1][2][4]. Company Overview - Intuitive, headquartered in Sunnyvale, California, is a leader in minimally invasive care and robotic surgery, with a focus on improving patient outcomes and care delivery efficiency [11]. - The company has developed the da Vinci surgical system, which has been used in nearly 17 million procedures over 30 years, training almost 90,000 surgeons [8]. Telesurgery Demonstration - The demonstration involved Dr. Doug Stoddard in Georgia and Dr. Andrea Pakula in France, using a dual console da Vinci 5 system to perform surgery on an advanced tissue model [2][3]. - The surgeons were able to exchange control of surgical instruments remotely, utilizing Force Feedback technology to simulate the sensation of operating on live tissue despite being over 4,000 miles apart [3]. Future of Telesurgery - Intuitive's CEO emphasized the potential of telesurgery to enhance patient access to care, while also noting the importance of careful development in infrastructure and technology to ensure safety and reliability [4][6]. - The company is focused on building a robust network infrastructure to support telesurgery, rather than being the first to market [7]. Technology Development - The telesurgery software demonstrated is still in development and not yet cleared for sale or use in the U.S. or EU, indicating ongoing efforts to ensure safety and effectiveness [9]. - Intuitive's telecollaboration suite includes telementoring and teleproctoring, aimed at improving clinical outcomes and reducing care costs [6].
SeaStar Medical Grows Customer Base and Expands QUELIMMUNE Surveillance Registry
Globenewswire· 2025-07-16 12:45
Core Insights - SeaStar Medical Holding Corporation has expanded its QUELIMMUNE therapy user base by adding a recognized Texas-based children's hospital, which is significant for treating pediatric patients with ultra-rare Acute Kidney Injury (AKI) [1][5] - The QUELIMMUNE therapy was approved by the FDA in 2024 under a Humanitarian Device Exemption to address life-threatening AKI due to sepsis or septic conditions [1][5] - The SAVE Surveillance Registry has been established to monitor safety and outcomes for pediatric patients treated with QUELIMMUNE compared to standard care, with early data analysis expected to be presented at an upcoming medical conference [2][3] Company Developments - SeaStar Medical is making progress in introducing QUELIMMUNE to top children's hospitals in the U.S. and is collecting significant data on its performance through the SAVE Surveillance Registry [3] - The company is conducting the NEUTRALIZE-AKI pivotal trial, which is evaluating the safety and efficacy of the Selective Cytopheretic Device (SCD) therapy in adults with AKI, with 119 out of 200 planned subjects enrolled [3][9] - SeaStar Medical has received FDA Breakthrough Device Designation for QUELIMMUNE and five other indications, which may facilitate faster approval and better reimbursement dynamics [11] Clinical Outcomes - Data from clinical studies indicate a 77% survival rate for patients treated with QUELIMMUNE, representing a 50% reduction in loss of life compared to historical data, with 87.5% of survivors achieving normal kidney function by Day 60 post-ICU discharge [7] - The NEUTRALIZE-AKI trial's primary endpoint includes a composite of 90-day mortality or dialysis dependency, with secondary endpoints assessing various health outcomes [9] Industry Context - AKI is characterized by a sudden loss of kidney function and can lead to severe complications, including multi-organ dysfunction and increased healthcare costs due to prolonged ICU stays and reliance on dialysis [4] - The QUELIMMUNE therapy is specifically designed for pediatric patients weighing 10 kilograms or more who are on antibiotics and receiving Renal Replacement Therapy in the ICU [5][10] - SeaStar Medical's SCD therapy aims to modulate the immune response to prevent destructive hyperinflammation, which is critical for improving outcomes in patients with AKI and other related conditions [10]
J&J(JNJ) - 2025 Q2 - Earnings Call Presentation
2025-07-16 12:30
Q2 2025 Financial Performance - Worldwide sales reached $23.7 billion, a 5.8% increase compared to Q2 2024, with operational sales growth of 4.6%[47] - U S sales increased by 7.8% to $13.5 billion in Q2 2025 from $12.6 billion in Q2 2024[47] - Adjusted earnings were $6.7 billion, and adjusted EPS was $2.77[49] - GAAP net earnings increased to $5.5 billion, a rise of 18.2%[49] Innovative Medicine - Innovative Medicine sales reached $15.202 billion, with operational growth of 3.8%[51] - Oncology sales grew by 22.3% operationally, reaching $6.312 billion[51] - Immunology sales declined by 16% operationally, totaling $3.993 billion, impacted by STELARA biosimilar competition[51] MedTech - MedTech sales were $8.541 billion, with operational growth of 6.1%[53] - Cardiovascular sales increased by 22.3% operationally, reaching $2.313 billion[53] - Orthopaedics sales decreased by 1.6% operationally, totaling $2.305 billion[53] Guidance - The company increased its operational sales guidance for 2025 to 4.8% and adjusted operational EPS guidance to 7.0% (midpoints)[62] - Operational sales are projected to be between $92.7 billion and $93.1 billion[62]
CVRx Announces Positive News on Outpatient Payment for Barostim
Globenewswire· 2025-07-16 11:30
Core Insights - CVRx, Inc. announced that the Centers for Medicare and Medicaid Services (CMS) proposed to maintain the Barostim implant procedure under the New Technology Ambulatory Payment Classification (APC) 1580, with an outpatient payment of approximately $45,000 [1] - The proposal follows positive reimbursement developments, including Barostim's assignment to a higher paying MS-DRG for inpatient procedures and its transition from Category III to Category I CPT codes for physician payments starting January 1, 2026 [2] - The updates in reimbursement are expected to enhance access to Barostim for patients with heart failure, supporting its broader market adoption and long-term growth [3] Company Overview - CVRx is a commercial-stage medical device company focused on innovative neuromodulation solutions for cardiovascular diseases [4] - Barostim is the first FDA-approved medical technology that uses neuromodulation to alleviate symptoms in heart failure patients, delivering electrical pulses to baroreceptors in the carotid artery [4] - Barostim has received FDA Breakthrough Device designation and is compliant with EU Medical Device Regulation, holding CE Mark approval for heart failure and resistant hypertension in the European Economic Area [4]