Remove 2024 Remove Immunization Remove Labelling
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Valneva submits application seeking FDA approval for IXCHIQ for adolescent use

Pharmaceutical Business Review

The label extension application is supported by positive Phase III data from adolescent trials reported in May this year. In the US and Canada, the application also includes two-year antibody persistence data, demonstrating that 97% of subjects maintained their immune response after 24 months.

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Getting Quality Supplements

The Thyroid Pharmacist

This is because I had learned about various adulterants found in supplements, how some supplement manufacturers don’t actually put the products that are on the label in the bottle, or that the dosages listed on the label may be completely different from what’s in the products. We have 95 expiring in March 2024.)

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Developing a new treatment paradigm for chronic kidney disease

European Pharmaceutical Review

To mark World Kidney Day 2024, Dr Marshall Fordyce, CEO of Vera Therapeutics, spoke with EPR about the challenges of treating kidney diseases, specifically IgAN, a condition caused by dysfunctional B cells. IgAN is the most common primary glomerulonephritis worldwide. Internet] Vera Therapeutics. cited 2024Mar].

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Developing a new treatment paradigm for IgAN

European Pharmaceutical Review

To mark World Kidney Day 2024, Dr Marshall Fordyce, CEO of Vera Therapeutics, spoke with EPR about the challenges of treating kidney diseases, specifically IgAN, a condition caused by dysfunctional B cells. IgAN is the most common primary glomerulonephritis worldwide. Internet] Vera Therapeutics. cited 2024Mar].

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Ichnos Glenmark Innovation presents first clinical data from phase 1 study of Trispecific TREAT Antibody, ISB 2001

Express Pharma

Initial results from 20 patients treated as of October 1, 2024, demonstrated an overall response rate (ORR) of 75 per cent (15/20) across all doses tested (0.005 to 1.2mg/kg), with a stringent complete remission (sCR) and complete remission (CR) rate of 20 per cent. No immune cell-associated neurotoxicity syndrome (ICANS) was observed.

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Eric Halioua, President & CEO at PDC*line Pharma Shares Insights on the Results from P-I/II Trial with PDC*lung01

PharmaShots

We are conducting an open-label, dose-escalation, phase I/II study PDC-LUNG-101 assessing the safety, tolerability, immunogenicity, and the preliminary clinical activity of therapeutic cancer vaccine PDC*lung, associated or not with anti-PD1 treatment in patients with non-small-cell lung cancer (NSCLC). 2015; Zhu et al., 2015; Zhu et al.,

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Covid-19 vaccine success bolsters nanoparticle drug delivery research

Pharmaceutical Technology

With early nanoparticle studies, researchers often found the human body’s innate immune response to drugs and the short-lasting effects of drugs challenging, as they can also reduce a drug’s efficacy. Since then, the drug has been used off-label in breast cancer and other types of cancer.