|
26-03-2021 15:03 |
|
EMA
issues advice on use of regdanvimab for treating COVID-19 |
|
EMA’s human medicines committee (CHMP) has completed its review on the use of the monoclonal antibody regdanvimab (also known as CT-P59) to treat patients with COVID-19. This review was undertaken to provide a harmonised scientific opinion at EU level to support national decision-making on the possible use of the antibody prior to marketing authorisation. The Agency concluded that regdanvimab can be used for the treatment of confirmed COVID-19 in adult patients who do not require supplemental oxygen therapy and who are at high risk of progressing to severe COVID-19. The medicine is given by
infusion (drip) into a vein and the proposed conditions of use are available here. EMA made its recommendations
following a review of data from an ongoing study looking into the effects of
regdanvimab in adult outpatients with COVID-19 symptoms described as mild to
moderate who do not need supplemental oxygen. Results from the first part of
the study indicate that regdanvimab may lower the rate of hospitalisation.
However, the results were not robust enough to reach a firm conclusion on the
medicine’s benefits at this point in time. In terms of safety, most side
effects reported were mild or moderate. Reactions related to the infusion
(including allergic reactions) cannot be excluded and healthcare
professionals should monitor patients for these reactions. Despite the uncertainties, the
CHMP concluded that regdanvimab can be considered a treatment option for
patients at high risk of progressing to severe COVID-19, based on a
reasonable likelihood that the medicine may provide clinical benefit, and a
low likelihood of harm. EMA’s recommendations can now
be used to support national advice on the possible use of this monoclonal
antibody before a marketing authorisation is issued. While the current evaluation
has concluded, a rolling
review of regdanvimab, which started on 24 February, is currently
ongoing. Once finalised, the rolling review will be the basis for an EU
marketing authorisation application for this medicine. More about the medicine Regdanvimab is a monoclonal
antibody with activity against SARS-CoV-2, the virus that causes COVID‑19. A
monoclonal antibody is a type of protein that has been designed to attach to
a specific structure (called an antigen). Regdanvimab has been designed to
attach to the spike protein of SARS-CoV-2. When it attaches to the spike
protein, the ability of the virus to enter the body’s cells is reduced. This
is expected to reduce the need for hospitalisation in patients with mild to
moderate COVID-19. More about the procedure The review of regdanvimab was
started at the request of the EMA Executive Director under Article
5(3) of Regulation 726/2004 following preliminary discussion with the
COVID-19 EMA pandemic task force (COVID-ETF), which brings together experts
from across the European medicines regulatory network to advise on the
development, authorisation and safety monitoring of medicines and vaccines
for COVID-19. The review of regdanvimab was
carried out by EMA’s Committee for Medicinal Products for Human Use (CHMP),
responsible for questions concerning medicines for human use, which has now
issued its scientific opinion. The CHMP’s scientific opinion can be taken
into account by EU member states and EMA when evaluating this medicine for
the treatment of COVID-19. (ΜΚΥ) |
