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Velocity Expands to 17 Sites in Europe

Velocity Clinical Research

The acquisition of KO-MED is Velocity’s first foray into Oncology research, which accounts for roughly 40-50% of clinical trials globally. In most cases, the participant of a clinical trial benefits from taking part, which is of great importance, especially in oncological trials. and Europe.

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MUSC is first in nation to enroll kids in trial of novel MIS-C therapy

Scienmag

Using an investigational cell therapy, Medical University of South Carolina pediatricians successfully treated two patients with multisystem inflammatory syndrome in children, a rare but life-threatening complication of COVID-19.

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Existing heart drugs may help cancer patients respond better to PD(L)1 immunotherapy

Scienmag

Researchers have found that a class of commonly-used heart drugs may also improve patients’ responses to anti-cancer immunotherapies called PD(L)1 inhibitors, according to preliminary findings to be presented at the 32th EORTC-NCI-AACR [1] Symposium on Molecular Targets and Cancer Therapeutics, which is taking place online.

Drugs 73
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Octapharma presents results of study on Octagam® 10% for severe COVID-19 patients at ASH

Scienmag

IVIg portfolio also featured in study design poster on primary infection prophylaxis in patients with chronic lymphocytic leukemia PARAMUS, N.J.

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Amarin Reports Third Quarter 2020 Financial Results and Provides Business Update

The Pharma Data

Expanded m edical society recommendations in support of the efficacy and safety of VASCEPA : The European Society of Cardiology expanded their guidelines to recommend use of VASCEPA in treating acute coronary syndrome patients. Patients with such allergies should discontinue VASCEPA if any reactions occur. VASCEPA.

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Octapharma presents research on congenital & acquired bleeding disorders at ASH Meeting

Scienmag

Research evaluates use of fibryga®, Octaplas™, and Octaplex® as investigational therapies PARAMUS, N.J.

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Top 30 Pharma and Biotech Companies in 2023: Statistics and Trends

XTalks

This is largely due to failed trials as a prophylaxis resulting in the European Committee for Medical Products (CHMP) recommending against the approval of Lagevrio. There was a record 34 approvals in major markets, and late-stage trials are commencing for medications including camizestrant, datopotamab deruxtecan and volrustomig.

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