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Leaving Johnson & Johnson to Join a Startup, This Scientist Aims to 'Revolutionize' Small-Molecule Drug Discovery

Murray McKinnon, who helped bring blockbuster drugs such as Stelara, Tremfya, and Remicade to market, has chosen to join Empress Therapeutics, a startup with fewer than 40 employees, after over 35 years at major pharmaceutical companies. The company, incubated by Flagship Pioneering, aims to use genetics to find small-molecule drugs within the human body. Its platform has already produced 15 molecules, with plans to submit multiple IND applications over the next 24 months.

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Rare disease researcher challenges disability discrimination in new lawsuit

Dr. Vivian Cheung is a rare disease researcher who herself has a rare disease, and she has filed a discrimination lawsuit against the Howard Hughes Medical Institute after her contract was not renewed in 2018. The case will go to trial on December 4. This article recounts her personal experiences, her laboratory's discoveries in RNA research, and the systemic neglect of disabled scientists in academia.

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Purpose Beyond Profit: This Pharmaceutical Company Tackles Critical Issues in Women's Health

On the first anniversary of the overturning of Roe v. Wade, Afaxys, a privately held pharmaceutical company named for 'affordability and accessibility,' is supplying oral contraceptives and other products to 8,400 health centers within the U.S. public health system through its unique low-margin, high-coverage model. CEO Ronda Dean, drawing from her own adolescent healthcare experiences, emphasizes the urgency of preserving the FDA approval system and the accessibility of reproductive health services.

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A Former Heavyweight Pharma Company Sets Out Again: The New Journey of Anti-TNF Therapy

This article reviews the journey of anti-TNF drugs from Centocor's failure to Remicade's success, and focuses on how 180 Life Sciences is extending this mature mechanism to new indications such as Dupuytren's contracture, postoperative cognitive decline, and frozen shoulder, while also developing synthetic cannabidiol analogs.

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What the 2014 Ebola Outbreak Taught This Biotech CEO About Communication

Colleen Acosta, CEO of Freya Biosciences, served as a WHO epidemiologist during the 2014 Ebola outbreak in West Africa. She applies the communication and persuasion skills learned from that experience to biotech entrepreneurship, including explaining science to investors, addressing skepticism, and advancing the development of microbial immunotherapy for women's health.

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From Battlefield to Pharma: An Army Officer's Mission Journey at GSK

From a tank commander in the Saudi desert to Senior Vice President of GSK's US Anti-Infectives and Respiratory business, Court Horncastle's career spans two seemingly disparate worlds. In the military, he learned to navigate and lead in extreme environments; in pharma, he has channeled that sense of purpose into relentless drive to advance antibiotic innovation and serve patients. This article reviews his transition journey, leadership philosophy, and GSK's strategic re-entry into infectious diseases in the era of antimicrobial resistance.

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Is the United States ready for a new type of opioid?

Against the backdrop of the lingering aftermath of the opioid crisis, Tris Pharma is advancing clinical development of the new painkiller cebranopadol. The drug targets both NOP and MOP receptors, aiming to provide analgesic effects similar to traditional opioids while reducing side effects such as euphoria, respiratory depression, and physical dependence. The company's founder and CEO, Ketan Mehta, states that rebuilding industry trust is the biggest challenge and plans to present the drug's value through transparent data.

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BIO Interim Leader Rachel King: Stabilizing the Organization, Focusing on IRA and Accelerated Approval Are Top Priorities

Rachel King had already retired, but BIO's call brought her back to the industry frontline. Facing the turmoil following the former CEO's departure, her primary task is to stabilize the organization. Now, she is leading BIO in addressing the treatment disparities between small-molecule and large-molecule drugs under the Inflation Reduction Act, defending the FDA's accelerated approval pathway, while also paying attention to capital formation, workforce diversity, and PBM transparency.

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A Day in the Life of a Pharma Executive: Lyndra CEO Patricia Hurter

In the 'A Day in the Life of a Pharma Executive' series, we follow Lyndra Therapeutics CEO Patricia Hurter to see how she balances her equestrian hobby with company management, and review the company's recent progress in the Phase III trial of an oral once-weekly schizophrenia treatment, as well as her experience responding to the Silicon Valley Bank crisis.

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