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Merck and Moderna partner to develop and sell cancer vaccine

Pharmaceutical Technology

The mRNA-4157/V940 has been designed to stimulate an immune response by producing T-cell responses depending on the mutational signature of a patient's tumour.

Vaccines 115
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Positive results for mRNA vaccine in melanoma patients

European Pharmaceutical Review

When administered in the body, the RNA-encoded neoantigen sequences are endogenously translated and undergo natural cellular antigen processing and presentation, a key step in adaptive immunity. Keytruda is an immunotherapy that works by increasing the ability of the body’s immune system to help detect and fight tumour cells.

Vaccines 115
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Merck to develop mAb through $10.8b acquisition

European Pharmaceutical Review

I look forward to working with the Prometheus team to establish a new paradigm of precision treatment for immune diseases,” commented Dr Dean Y Li, President of Merck Research Laboratories. Prometheus is a clinical-stage biotechnology company. “I

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Show 1344: Managing Meat Allergy and Other Tick-Borne Diseases

The People's Pharmacy

Commins sees patients in the UNC allergy clinic and maintains an active research laboratory. His primary research and clinical interest is alpha-gal syndrome. Patients in the allergy clinic often have difficult to diagnose food allergies or allergic reactions. Photo by Chris Polydoroff.

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Japan grants approvals for Merck’s Keytruda to treat different cancers

Pharmaceutical Technology

An anti-programmed death receptor-1 (PD-1) therapy, Keytruda acts by boosting the immune system’s ability to find and fight tumour cells. With the latest development, the antibody is indicated for 23 usages in 13 different cancer types of cancer in the country.

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Keytruda approved as first-line advanced cervical cancer therapy

pharmaphorum

Some cancer cells contain large amounts of PD-L1, which helps them to evade the body’s immune system. Dr Roy Baynes, senior vice president and head of global clinical development, chief medical officer, Merck Research Laboratories, said the data showing a 36% reduction in the risk of death “are compelling”.

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US FDA grants approval for Merck’s pneumococcal vaccine for children

Pharmaceutical Technology

According to findings from a pivotal study, a four-dose paediatric regimen of Vaxneuvance induced immune responses non-inferior to the presently available 13-valent pneumococcal conjugate vaccine (PCV13) for the 13 shared serotypes.