The Skyrizi approval pairs an interleukin-23 antibody with an on-body injector for 720 mg subcutaneous induction in adults, per phase 3 AFFIRM data.
|Articles|January 15, 2002
- BioPharm International-01-01-2002
- Volume 15
- Issue 1
Systematic Troubleshooting for LC/MS/MS: Part 2, Large-Scale LC/MS/MS and Automation
Author(s)Timothy D.J. Halls, Naidong Weng
by Naidong Weng and Timothy D.J. Halls, Covance Laboratories, Inc. Meeting the challenges of large-scale LC/MS/MS can improve the analytical processes that support biopharmaceutical drug development. The conclusion of this article presents troubleshooting techniques for LC/MS/MS and illustrates an automation strategy.
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Outsourcing Outlook: E-Sourcing, Internet Facilitates Flexible Collaborationalmost 25 years ago
Inside Washington: Biotechnology in the Limelight, the Year Aheadalmost 25 years ago
Your Vested Interests: The War of the Westalmost 25 years ago
Statistics for Laboratory Method Comparison Studiesalmost 25 years ago
From the Editor: Farewell to 2001 . . . Our Biotech Odyssey Continuesalmost 25 years ago
Liposomes (a Review): Part Two, Drug Delivery Systemsalmost 25 years ago
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Gilead agrees to acquire PepStar’s oral IL-23R peptide program for $1.275 billion, Zymeworks licenses its DLL3-targeted trispecific T-cell engager ZW209 to Roche, and the US Treasury proposes adding biotechnology to its outbound investment restrictions.
FNIH CEO Dr Julie Gerberding will open the October 25-28 meeting with a talk on using AI, adaptive trials, and alternative methods in drug development.
Insilica's Dr Thomas Luechtefeld argues process traceability, not benchmark accuracy alone, determines whether AI toxicology decisions can be trusted.
Phase 1 HCXT-2001, an oral macrocyclic IL-23R peptide, could be paired with emvistegrast as a daily oral IBD treatment, according to Gilead.
Roche gains exclusive global rights to ZW209, a DLL3×CD3×CD28 trispecific T-cell engager designed for CD28 co-stimulation. A phase 1 study in small cell lung cancer and other neuroendocrine tumors is underway.
A Treasury proposed rule would restrict certain US investments in biotechnology in China and other countries of concern, raising questions about how cross-border licensing and joint venture deals will be treated.
Nate Edwards of Arya Consulting moderates a discussion with Elisabeth Gardiner of Tevard Biosciences and Donny Xu of the RTW Institute about the regulatory and manufacturing hurdles facing rare disease drug developers.
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