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Beyond the Lab: Cell & Gene Therapy

Drug Target Review

Dear Readers, I am thrilled to announce the launch of our new series, “Beyond the Lab,” which promises to deliver high-level insights commissioned exclusively by Drug Target Review magazine. Emerging Trends and Technologies The report highlights the latest emerging trends and technologies in cell and gene therapy.

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Mediating BRAF-mutant melanoma resistance

Drug Target Review

Regarding therapy resistant melanomas, why is the alteration of the epigenetic landscape considered significant, and what has been lacking in terms of validated targetable epigenetic mechanisms? What is remarkable here is that we show that the addition of corin to BRAFi-resistant tumour cells resensitises them to BRAFi therapies.

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Women in Stem with Leila Jaafar

Drug Target Review

He would return from his travels with an assortment of magazines, often including a scientific journal in the mix. As CEO, Leila focuses on shaping and the execution of NUCLIDIUM`s international strategy towards its primary goal of improving the availability and affordability of radiopharmaceuticals in cancer diagnosis and therapy worldwide.

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The Art of Recruitment and Talent Development in FSPs

PPD

In addition, functional and therapeutic area tools (like our comprehensive cell and gene therapy training and forums), resources and role-specific trainings (including our CRA Academy) support employees throughout the entire project life cycle — from startup and maintenance to closeout — to provide ongoing guidance and support.

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Tomorrow’s Innovators to Create Custom Biopharma Educational Programming and Increase Recruitment of Black Talent in the Biopharma Industry

The Pharma Data

and the Doctor of Physical Therapy. About North Carolina Agricultural and Technical State University North Carolina Agricultural and Technical State University is the nation’s largest historically Black university, as well as its top ranked (Money magazine, Best Colleges). The three professional degrees include the J.D.,

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Rapid delivery of toxicological material

Drug Target Review

Network Pharma Magazine. Alejandro has over 15 years of experience in Biopharma working in R&D and commercial areas, where he has supported the development of a wide range of products (eg, complex recombinant proteins, AAV and cell-based therapies) and led efforts for smart biomanufacturing. 2023 Jan-Dec;15(1):2220150.

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Article FDA Thank You The FDA rejected a psychedelic sponsor’s bid for approval. Here are six industry takeaways

Agency IQ

However, the agency can describe a concomitant therapy in labeling for a product it has authority to regulate if it is essential for the therapeutic effect. While the ability to describe and specify aspects of the therapy is limited, the agency can specify the number and licensure of therapists who would participate in the MDMA treatment.

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