
|Articles|June 1, 2014
- BioPharm International-06-01-2014
- Volume 27
- Issue 6
TOC Analyzer Increases Productivity
TOC Analyzer Increases Productivity
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GE’s Sievers M9 Total Organic Carbon (TOC) Analyzer is designed to measure TOC in a range of samples from ultrapure water to process waters. GE offers the Sievers M9 TOC Analyzer in three versions: portable, online, or laboratory. The M9 Analyzer increases productivity by producing TOC results in two minutes. According to the company, the M9 enhancements promote simple operation and optimal data utilization. In addition, the M9 Analyzer can measure conductivity in grab sample or autosampler modes, an upgrade from the 900 TOC Analyzer series.
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A Sampling of New Tools for Downstream Processingover 12 years ago
Finished Product Monographs in the European Pharmacopoeiaover 12 years ago
Global Expansion Shapes Drug Oversightover 12 years ago
Bureaucratic Roadblocks Threaten Biopharma Growthover 12 years ago
Outsourcing No Longer Just for Cost-Cuttingover 12 years ago
Challenges in Analytical Method Development and Validationover 12 years ago
Brunei's Potential Pharmaceutical Market Growthover 12 years ago
Assuring Equivalency of Alternative Lot-Release Test Methodsover 12 years ago
Handheld Analyzer Improves AccuracyAdvertisement
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argenx agrees to acquire macrocyclic peptide developer Unnatural Products for up to about $1.15 billion, Johnson & Johnson’s pasritamig and JNJ-9401 bispecific regimen achieves a 73% PSA response in phase 1 in metastatic castration-resistant prostate cancer, and Janux Therapeutics’ TRBV6-targeted T-cell engager JANX011 shows deep B-cell depletion in healthy volunteers.

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argenx's acquisition of Unnatural Products adds macrocyclic peptides that could yield oral or long-acting treatments for immune-mediated diseases.

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In a phase 1 study, Johnson & Johnson’s combination of pasritamig and JNJ-9401, two bispecific antibodies targeting KLK2 and PSMA, cut PSA by at least 50% in 73% of patients with metastatic castration-resistant prostate cancer. The regimen is now in phase 3.

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FDA grants accelerated approval to Johnson & Johnson’s subcutaneous EGFR/MET bispecific Rybrevant Faspro for previously treated head and neck squamous cell carcinoma, T-Therapeutics raises a $133 million Series B to take TCR-CD3 bispecifics into clinical trials, and Alethio Therapeutics raises a $90 million Series A to advance its first-in-class G6B antibody for essential thrombocythemia.
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