What good is working without a window to look out of? As I look out of mine (at my work-in-progress back garden), it’s good to see the early signs of Spring.
A similar optimism, I’m noticing, is getting around the pharmaceutical industry as players and stakeholders continue to band together in the aim of making lives around the world better, despite ongoing challenges such as COVID-19, and emerging challenges such as the Marburg outbreak being witnessed in Equatorial Guinea, for which the WHO has intensified its vigilance. Bird flu strains being found in other species will present another challenge, but these are the reasons why young researchers chose a profession in medicine; these are the challenges that drive them. These are the legacies they hope to leave to the new generations that follow. I’m looking forward to hearing more of the new ideas and approaches from young scientists and CEOs as the days begin to get warmer, brighter, and fresher.
New European Union (EU) Health Technology Assessment (HTA) regulation was enacted in January 2022 to help streamline the clinical assessment process for EU member states' HTA bodies. Read how manufacturers can navigate these changes effectively during clinical development & market access planning.
Breaches of code lead to APBI President resignation
Pinder Sahota, General Manager, Novo Nordisk UK, has stepped down as President of the ABPI over concerns that an ongoing process concerning Novo Nordisk breaches of the ABPI Code of Practice would distract from the ABPI’s work. ABPI Vice President Susan Rienow will temporarily assume responsibilities. Novo Nordisk was found to be in violation of the ABPI code recently, in addition to “multiple breaches” reported last year. Continue reading
Technology to take on brain cancer
A joint research project between Yale and the University of Connecticut has developed a nanoparticle-based treatment that targets multiple culprits in glioblastoma. Published in Science Advances, results show that the new treatment uses bioadhesive nanoparticles that adhere to the site of the tumor before releasing synthesized peptide nucleic acids, which target the overexpressed microRNAs “oncomiRs” that cause the proliferation of cancer cells and tumor growth. The researchers are seeking to improve therapeutic approaches for targeting the molecular genetic mediators of glioblastoma. Continue reading
Also in the News...
Gavi approves appointment of Muhammad Ali Pate as CEO; Seth Barkley to step down in August after 12 years as the Vaccine Alliance chief.
FDA grants full approval for GSK’s Jemperli for adults with recurrent or advanced mismatch repair-deficient endometrial cancer.
Takeda announces acquisition of all shares of Nimbus Lakshmi from Nimbus Therapeutics, following clearance from US FTC.
Catalent completes $2.2 million expansion to clinical supply facility in Singapore. The CDMO will install 35 freezers for storage for the support of advanced modalities, including mRNA-based vaccines.
FDA grants pediatric approval of Regeneron’s EYLEA (aflibercept) injection to treat preterm infants with retinopathy of prematurity. EYLEA is now indicated to treat five retinal conditions.
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