
Furmonertinib is in development for the treatment of advanced or metastatic non-small cell lung cancer with epidermal growth factor receptor exon 20 insertion mutations.

CRISPR Therapeutics Announces Completion of FDA Advisory Committee Meeting for Exagamglogene Autotemcel for Severe Sickle Cell Disease

Furmonertinib is in development for the treatment of advanced or metastatic non-small cell lung cancer with epidermal growth factor receptor exon 20 insertion mutations.

The approval of pembrolizumab (Keytruda; Merck) combined with gemcitabine and cisplatin for the treatment locally advanced unresectable or metastatic biliary tract cancer is the sixth sixth indication for the anti-PD-1 therapy for gastrointestinal cancers.

In the ever-evolving landscape of healthcare, it's vital for organizations to take steps toward bridging the gap between their clinical and marketing teams.

Surge acted as a precursor for the RSV-marketed drug landscape in 2023, says GlobalData.

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Gill discusses her continuing work to transform clinical trials and improve the patient experience through DCTs.

Clinical studies are increasingly designed to satisfy evidentiary needs.

In this Q&A with Pharmaceutical Executive®, Andrew Hopkins, founder and CEO of Exscientia, reveals how artificial intelligence (AI) is currently being utilized in the pharma industry, predictions for where AI can be implemented in the future, and what pharma fears most about AI.

The current vaccine pipeline brings promise of significant global health advancements—yet development gaps remain, and the future delivery challenges must be considered.

Companies that understand the regulatory environment in Europe can keep their trials on budget and on schedule.

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In this Q&A, Matt Smith, vice president of research site development, Slope, discusses the competition pharma companies and trial sponsors face when trying to become a sponsor of choice and build trust with sites and patients.

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Expansion aims to continue to create programs that address health and education inequities.

Elizabeth (Beth) Garner, chief scientific officer for Ferring Pharmaceuticals, discusses what it was like transitioning from working as a gynecologic oncologist and seeing patients to working in pharma, specifically clinical trials.

First guidance in this area from the Agency addresses the unique challenges when designing clinical studies for these drugs

Christon Hill, chief innovation officer, SERB Pharmaceuticals, reveals the demand for antidotes, the process of financial backing, administration needs, as well as antidotes the company is working on, including antidotes for toxins, infectious diseases, biological agents, and drug toxicities.

When deciding on the right commercialization model, organizations must consider multiple factors, including the asset or platform they possess, the launch timing, the funding required, and staffing expertise.

O'Neill discusses the company's place in the global market and recent advancements to improve the patient experience.

Panel discusses what real-world evidence—and related patient-reporting technology—need to achieve to better influence payer decision-making.

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