Celltrion COVID-19 drug Regkirona (regdanvimab) was approved by EU
- Early Biomarker for Multiple Sclerosis Development Identified Years in Advance
- Aspirin Found Ineffective in Improving Recurrence Risk or Survival Rate of Breast Cancer Patients
- Child Products from Aliexpess and Temu Contain Carcinogens 3026x Over Limit
- Daiichi Sankyo/AstraZeneca’s Enhertu Shows Positive Results in Phase III DESTINY-Breast06 Clinical Trial
- Mn007 Molecules Offer Potential for Combating Streptococcus pyogenes Infection
- Popular Indian Spices Banned in Hong Kong Over Carcinogen Concerns
Celltrion COVID-19 drug Regkirona (regdanvimab) was approved by EU
- AstraZeneca Admits for the First Time that its COVID Vaccine Has Blood Clot Side Effects
- Was COVID virus leaked from the Chinese WIV lab?
- HIV Cure Research: New Study Links Viral DNA Levels to Spontaneous Control
- FDA has mandated a top-level black box warning for all marketed CAR-T therapies
- Can people with high blood pressure eat peanuts?
- What is the difference between dopamine and dobutamine?
- How long can the patient live after heart stent surgery?
Celltrion COVID-19 drug Regkirona (regdanvimab) was approved by EU. Celltrion monoclonal antibody drug Regkirona (regdanvimab) was approved by EU to treat high-risk COVID-19 patients!
Regkirona is used to treat adult patients who do not require supplemental oxygen and are at high risk of developing severe COVID-19 disease.
According to Baidu’s “New Coronavirus Pneumonia Epidemic Real-time Big Data Report”, as of 01:00 on November 17, 2021, more than 250 million cases (254 million) have been diagnosed globally . There were more than 5.12 million deaths.
Recently, the Korean biopharmaceutical company Celltrion Group announced that the European Commission (EC) has approved Regkirona (regdanvimab, CT-P59) for the treatment of COVID-19 adult patients who do not require supplemental oxygen and have an increased risk of developing serious diseases .
Currently, Regkirona has not been approved by the US FDA, but Celltrion is discussing with the FDA to submit an emergency use authorization (EUA) application.
Regkirona is one of the first monoclonal antibody drugs granted marketing authorization by the European Union .
In the same week, the European Union approved the Roche/Regeneron antibody cocktail therapy Ronapreve (casirivimab and imdevimab, formerly known as REGN-COV2) :
(1) For the treatment of COVID-19 that does not require oxygen supplementation and has an increased risk of developing a serious disease Adults and adolescents (age ≥ 12 years old, weight ≥ 40 kg) patients;
(2) For people ≥ 12 years old and weight ≥ 40 kg to prevent COVID-19 (pre-exposure or post-exposure prevention).
Regkirona and Ronapreve’s approval decision was made immediately after the European Medicines Agency (EMA) Committee for Medicinal Products for Human Use (CHMP) issued a positive review opinion on November 11, reflecting that EMA and EC will Shortening the review time for safe, effective, and high-quality therapies is a priority.
Under normal circumstances, if the CHMP issues a positive review opinion on the drug, the EC will usually make a review decision within 1-2 months.
A monoclonal antibody is a protein designed to attach to a specific target. In this case, it is the spike protein of the new coronavirus (SARS-CoV-2). Its role is to block the virus’s way into human cells. .
The EU approved Regkirona, based on data from a global phase 3 clinical trial . The trial involved 1,315 people in 13 countries including the United States, Spain, and Romania, and evaluated the efficacy and safety of Regkirona.
Data show that for patients who are at high risk of developing severe COVID-19, Regkirona treatment significantly reduces the risk of COVID-19-related hospitalization or death by 72% .
(source:internet, reference only)
Disclaimer of medicaltrend.org
Important Note: The information provided is for informational purposes only and should not be considered as medical advice.