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Amgen's VESALIUS-CV Data Push Repatha Into Earlier Cardiovascular Prevention

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Amgen’s VESALIUS-CV Data Push Repatha Into Earlier Cardiovascular Prevention

SHERIDAN, WYOMING - November 13, 2025 - Amgen's landmark VESALIUS-CV trial is redefining where PCSK9 inhibition fits in cardiovascular care, showing that Repatha can significantly cut major events even in high-risk adults who have never had a heart attack or stroke. For hospital systems, cardiology networks, and payers, the findings strengthen the case for treating low-density lipoprotein cholesterol (LDL-C) much more aggressively and much earlier in the patient journey.

Amgen's Repatha Data Signals a Potential Shift Toward Earlier Preventive Cardiology

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Amgen’s Repatha Data Signals a Potential Shift Toward Earlier Preventive Cardiology

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Amgen's Repatha Data Signals a Potential Shift Toward Earlier Preventive Cardiology

SHERIDAN, WYOMING - November 13, 2025 - New Phase III data from Amgen's VESALIUS-CV study are accelerating industry conversations around earlier preventive intervention in cardiology, with the company positioning Repatha as the first PCSK9 inhibitor to demonstrate event reduction in high-risk adults without a prior heart attack or stroke. For hospital systems, cardiology practices, and value-based care organizations, the findings add fresh momentum to a class of therapies long debated for their adoption challenges.

J&J's Darzalex Faspro Wins First-Ever FDA Approval for Smoldering Multiple Myeloma

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J&J’s Darzalex Faspro Wins First-Ever FDA Approval for Smoldering Multiple Myeloma

SHERIDAN, WYOMING - November 10, 2025 - Johnson & Johnson has secured a major regulatory milestone for its oncology portfolio, with the U.S. Food and Drug Administration granting approval for Darzalex Faspro in patients with high-risk smoldering multiple myeloma. The expansion marks the first-ever therapy authorized for this pre-malignant stage of the disease, reinforcing J&J's leadership in hematologic oncology and enabling earlier clinical intervention to delay disease progression.

A Landmark Step Toward Early Intervention in Myeloma

Darzalex Faspro's new indication targets adults with high-risk smoldering multiple myeloma-patients statistically more likely to develop active disease within two years of diagnosis. By offering the first approved option at this pre-symptomatic stage, J&J is advancing a proactive "disease interception" approach that could reshape treatment timelines for oncologists and hematology practices.

Illinois’ Life Sciences Sector Shows Steady Job Market Growth

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SHERIDAN, WYOMING – July 21, 2025 – Illinois' life sciences industry continues to demonstrate resilience and growth, underlining the state's standing as a regional powerhouse in biopharma employment. According to 2024 data from BIO and TEConomy Partners, Illinois employed 93,402 bioscience professionals across 4,926 businesses, marking a 7.5% increase in employment since 2019 — a growth trajectory that positions the state as a key hub within the BioMidwest Hotbed.

Steady Hiring Momentum in 2025

Biopharma Talent Strategies Shift as Fractional Roles Gain Momentum

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SHERIDAN, WYOMING – July 21, 2025 – Facing industry-wide uncertainty and hiring slowdowns, biopharma companies are increasingly turning to fractional roles to fill critical talent gaps—an emerging trend reshaping workforce strategies across the sector. Recent insights from recruiters and professionals reveal a growing openness to flexible, project-based roles that offer companies agility while providing experienced professionals with continued engagement in the field.

Fractional Work Gains Traction Amid Market Challenges

A July LinkedIn poll conducted by BioSpace indicated that 22% of respondents have experience with fractional roles, while an additional 54% are considering them. This shift is driven largely by a tightening job market and prolonged hiring timelines.

AI-Driven Biotech Unicorns Face Tough Market as IPO Pathways Remain Uncertain

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SHERIDAN, WYOMING – July 21, 2025 – The latest generation of biotech unicorns is navigating a challenging financial landscape, as AI-powered drug discovery ventures encounter tight investment conditions and a shrinking pool of exit opportunities. While their billion-dollar valuations once promised swift IPOs, today's market demands more strategic flexibility, operational discipline, and differentiated technologies.

Valuations Under Pressure in a Binary Outcome Industry

Valuations in biotech remain inherently speculative, often hinging on clinical outcomes that may take over a decade to materialize. “Biotech valuations remain speculative bets on binary clinical outcomes that typically take 10 to 15 years to materialize,” said Kaz Helal, senior biotech analyst at PitchBook. “Most biotechs only prove their true worth when Big Pharma writes the check at exit.”

Women Leaders Driving Billion-Dollar Biotech M&A Deals

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SHERIDAN, WYOMING – July 21, 2025 – In a market often defined by bold strategies and high-stakes negotiations, five biotech CEOs have recently steered their companies into billion-dollar acquisitions — and each of them is a woman. These industry leaders not only shaped breakthrough therapies but also orchestrated some of the most high-profile M&A deals of recent years, underscoring the growing influence of women in biotech leadership.

Intra-Cellular Therapies: Sharon Mates’ Strategic Vision Realized in $14.6 Billion J&J Acquisition

Sharon Mates, founder, chairman, and CEO of Intra-Cellular Therapies, led the company from its 2002 inception to this year’s landmark $14.6 billion acquisition by Johnson & Johnson. Mates guided Intra-Cellular through key milestones, including FDA approvals for its atypical antipsychotic Caplyta in 2019 and 2021.

Acadia Charts Growth with Leadership Duo, Pipeline Push, and Strategic Focus on Rare Neurological Diseases

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SHERIDAN, WYOMING – July 21, 2025 – Acadia Pharmaceuticals has presented an ambitious vision to transform itself from a small biotech player into a recognized powerhouse, leveraging a sharpened leadership focus and a pipeline with multi-billion-dollar potential. Marking a milestone in its 32-year history, the company recently hosted its inaugural R&D Day, unveiling strategic plans aimed at driving up to $12 billion in annual pipeline-driven revenue.

Leadership Duo Drives Strategic Realignment

Obesity Drug Development Shifts Toward Muscle Preservation and Next-Generation Targets

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SHERIDAN, WYOMING – July 21, 2025 – The American Diabetes Association’s 2025 Scientific Sessions spotlighted the evolving priorities of obesity drug development, emphasizing muscle preservation, improved tolerability, and novel molecular targets. With global analysts projecting the anti-obesity market to exceed $150 billion annually by the early 2030s, biopharmaceutical companies are racing to innovate beyond first-generation GLP-1 therapies.

Obesity Treatment Leaders Refocus on Patient Experience

Audrey Greenberg Joins Mayo Clinic Ventures After Pioneering Biomanufacturing Success

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SHERIDAN, WYOMING – July 21, 2025 – Audrey Greenberg, known for transforming the cell and gene therapy manufacturing landscape, has embarked on a new chapter as partner at Mayo Clinic’s newly established venture arm. Her move follows a career of strategic pivots across finance, real estate, and biomanufacturing — each driven by an unwavering focus on creating meaningful impact.

From Wall Street to Purpose-Driven Ventures

Greenberg’s professional journey began on Wall Street, a path she reconsidered after witnessing the 9/11 attacks firsthand. "I watched the towers fall, and I thought, what do I want to do that actually makes an impact on society, instead of just moving other people’s money around?" she reflected. This question led her to launch a real estate venture focused on tax credit housing, developing shelters for battered women and affordable housing for seniors in underserved communities.