EMA Recommends Gohibic for ARDS Induced by SARS-CoV-2

You May Be Interested In:Match Day: Anesthesiology Still Hot, Family Med Is Not


Following a consultation with its emergency task force, the European Medicines Agency (EMA) has backed a drug for adult patients with acute respiratory distress syndrome (ARDS) induced by the SARS‑CoV-2 virus.

As a result, the EMA’s Committee for Medicinal Products for Human Use recommended granting a marketing authorization “under exceptional circumstances” for Gohibic (vilobelimab).

Gohibic is a recombinant chimeric monoclonal IgG4 antibody that binds to and blocks activity of the human complement factor C5a receptor. In reaching its decision, the committee considered evidence that showed patients with ARDS who also receive corticosteroids had reduced mortality at days 28 and 60 after starting treatment with Gohibic when compared with standard of care.

Side Effects and Administration

The most common side effect associated with Gohibic is pneumonia, reported in 21.7% of patients. Other negative effects are herpes simplex (6.3%), bronchopulmonary aspergillosis (5.7%), and sepsis (5.1%).

The full indication for Gohibic is as a treatment for adult patients with SARS‑CoV-2‑induced ARDS who are receiving systemic corticosteroids as part of standard of care as well as invasive mechanical ventilation with or without extracorporeal membrane oxygenation.

Gohibic will be available in the form of a 200 mg concentrate for solution for infusion. 

The committee specified that injection with Gohibic should be initiated and monitored by a physician experienced in the management of patients treated in an intensive care unit setting.

Exceptional Authorizations

Marketing authorizations can be recommended by the EMA in exceptional circumstances when an applicant can show that provision of comprehensive data on a medicine is not possible due to the rarity of the condition it is intended for, limited scientific knowledge, or ethical considerations in collecting data.

A final decision on a marketing authorization is now in the hands of the European Commission.

Peter Russell has been a journalist for 40 years covering international news, health, medicine, and national politics on radio, TV, and online. He is based in the UK. 

share Paylaş facebook pinterest whatsapp x print

Similar Content

Readers Embrace 'Going It Alone' Series on Aging and Chastise Makers of Pulse Oximeters - KFF Health News
Readers Offer Their Takes on the Opioid Crisis, Family Doctor Shortage, and Vaccine Policies – KFF Health News
A digital illustration of the United States where 12 states are highlighted and a magnifying glass focuses on Missouri where text from an opioid settlement fund report is shown within the state borders.
12 States Promised To Open the Books on Their Opioid Settlement Funds. We Checked Up on Them. – KFF Health News
T-DM1 Boosts Survival in HER2-Positive Breast Cancer
T-DM1 Boosts Survival in HER2-Positive Breast Cancer
Will Stem Cell Clinics Flourish Under RFK Jr.?
Will Stem Cell Clinics Flourish Under RFK Jr.?
FDA updates food import alerts for unapproved drugs, heavy metals and more
Sunway Medical to test surgical robots and more robotics briefs
Sunway Medical to test surgical robots and more robotics briefs
Today's Insight | © 2024 | News