Skip to main content

Helixgate

Skip to main content

Helixgate

Uncategorized

STAT+: Pharmalittle: We’re reading about a big Roche investment in the U.S., estrogen patch shortages, and more

And so, another working week will soon draw to a close. Not a moment too soon, yes? This is, you may recall, our treasured signal to daydream about weekend plans. Our agenda is still in the works, but we do plan to promenade extensively with the official mascots, catch up on our reading, welcome our vacuum cleaner back home, and hunt for the perfect iced coffee. We also hope to hold yet another listening party, where the rotation will likely include this, this, this, this and this. And what about you? If weather permits, the possibilities are endless — you could hike trails, stroll boardwalks, stop by a favorite restaurant, or take a long drive to nowhere. Well, whatever you do, have a grand time. But be safe. Enjoy, and see you soon. …

Heidi Overton’s years of loyalty to President Trump helped her become his pick to lead the U.S. Food and Drug Administration, but that devotion could ruin her chances at Senate confirmation, Politico explains.  Sen. Bill Cassidy (R-La.), a vaccination proponent who chairs the Health, Education, Labor and Pensions Committee, already signaled she may not have his vote. Another stumbling block: Many in the Make America Healthy Again coalition dislike her for backing Trump’s decision to protect the manufacturing of a weedkiller they believe causes cancer.

Drugmakers continue to face severe supply constraints for transdermal estrogen patches as demand surges, The Hill writes. The problem began last November, when the FDA began removing some of the strongest safety label warnings from hormone replacement therapy, which triggered a surge in prescriptions. But the patches are complicated to make and take considerably longer to manufacture than traditional pills. Limited manufacturing capacity has meant that many women are switching brands and dosages.

Continue to STAT+ to read the full story…

Read More

Published

on

And so, another working week will soon draw to a close. Not a moment too soon, yes? This is, you may recall, our treasured signal to daydream about weekend plans. Our agenda is still in the works, but we do plan to promenade extensively with the official mascots, catch up on our reading, welcome our vacuum cleaner back home, and hunt for the perfect iced coffee. We also hope to hold yet another listening party, where the rotation will likely include this, this, this, this and this. And what about you? If weather permits, the possibilities are endless — you could hike trails, stroll boardwalks, stop by a favorite restaurant, or take a long drive to nowhere. Well, whatever you do, have a grand time. But be safe. Enjoy, and see you soon. …

Heidi Overton’s years of loyalty to President Trump helped her become his pick to lead the U.S. Food and Drug Administration, but that devotion could ruin her chances at Senate confirmation, Politico explains.  Sen. Bill Cassidy (R-La.), a vaccination proponent who chairs the Health, Education, Labor and Pensions Committee, already signaled she may not have his vote. Another stumbling block: Many in the Make America Healthy Again coalition dislike her for backing Trump’s decision to protect the manufacturing of a weedkiller they believe causes cancer.

Drugmakers continue to face severe supply constraints for transdermal estrogen patches as demand surges, The Hill writes. The problem began last November, when the FDA began removing some of the strongest safety label warnings from hormone replacement therapy, which triggered a surge in prescriptions. But the patches are complicated to make and take considerably longer to manufacture than traditional pills. Limited manufacturing capacity has meant that many women are switching brands and dosages.

Continue to STAT+ to read the full story…

Read More

Continue Reading
Click to comment

Leave a Reply

Your email address will not be published. Required fields are marked *

Uncategorized

New webinar: Tackling drug discovery challenges in cancer research

Published

on

Cancer cells

Hosted by Drug Discovery World and supported by Sartorius and BioIVT, this webinar will explore the opportunities and challenges that exist within cancer research drug discovery and development.

You will hear from Dr Sudha Rao, Chief Scientific Officer of Kazia Therapeutics, Karol Budzik, PhD, Business Development Associate at Vyriad Therapeutics and Lars van der Veen, Chief Scientific Officer at iOnctura.

Presentations will cover how cancer treatments have shifted towards reprogramming the biology driving tumour growth, immune escape and treatment resistance, the trajectory that in vivo CAR-T treatments are taking, and how challenging tumours burdened by stroma and immune-mediated resistance can be tackled.

Q&A with the speakers follows the presentations.

Register for free now.

The post New webinar: Tackling drug discovery challenges in cancer research appeared first on Drug Discovery World (DDW).

Continue Reading

Uncategorized

Psilocybin proves promising in neuropathic pain mouse study

Published

on

Amid the rise of psychedelics in the mental health space, researchers have begun to explore psilocybin as a treatment for chemotherapy-induced peripheral neuropathy.

Continue Reading

Uncategorized

New Spectrometry Technique Could Aid Formulation Development

New Spectrometry Technique Could Aid Formulation Development

Published

on

A new technique combining two forms of spectrometry could help biopharmaceutical companies improve their choice of formulation buffer for antibody manufacturing by revealing how molecular forms and three-dimensional shapes of complex biologics respond to their environment. That’s the view of Christian Bleiholder, PhD, a professor at Florida State University who helped develop the technique.

According to Bleiholder, what happens structurally when a complex biological molecule, such as an antibody or viral spike protein, binds to its target is currently poorly understood.

“This is where [this approach] can help with the bioprocessing and formulation,” he says, as structural changes “can affect the lifespan [of the product] and lead to issues, such as aggregation.”

Because antibodies are complex, existing techniques tend to be powerful at different levels of complexity, he explains. Mass spectrometry is particularly powerful for distinguishing molecular composition, while structural approaches such as X-ray crystallography and cryo-electron microscopy can provide high-resolution structural information.

The challenge is understanding the link between these things within a heterogeneous sample, he says.

To overcome this, Bleiholder and his team worked with Bruker Daltonics to develop Tandem-Trapped Ion Mobility Spectrometry (Tandem-TIMS). This combines tandem ion mobility spectrometry with tandem mass spectrometry to disentangle three overlapping layers of molecular complexity: molecular form, three-dimensional shape, and binding or assembly state, he says.

He explains that, if the proteins have different structures, they can be characterized with tandem ion mobility spectrometry, and then mass spectrometry can be used to look at their molecular forms and binding states.

Going forward, Bleiholder hopes the technique can be used for formulation development but also earlier, during drug discovery of new products, such as multi-specific antibodies, to determine which molecular states are important and how those change when a biologic engages its target. He also plans to look at automating the technique.

Bleiholder spoke about using Tandem-TIMS at the Bioprocessing Summit in Boston earlier this year.

The post New Spectrometry Technique Could Aid Formulation Development appeared first on GEN – Genetic Engineering and Biotechnology News.

Continue Reading

Trending

Helixgate Biotech Review July Issue QR CodeScan to Read