Sunday, July 05, 2020 11:10:46 AM
IL-6 hypothesis looking shaky as Kevzara fails COVID-19 trialPhil TaylorPhil TaylorJuly 3, 2020
Hopes that already-approved drugs targeting IL-6 could be repurposed to treat COVID-19 have been undermined by disappointing results from the first large-scale trial of Sanofi and Regeneron’s Kevzara.
The two drugmakers have revealed that adding a 400mg daily dose of Kevzara (sarilumab) to standard care for COVID-19 patients on mechanical ventilation didn’t improve the main outcome goal.
The primary measure in the study was the percentage of those who achieved at least a one-point change from baseline on a seven-point scale, ranging from death to discharge from hospital.
While there were “minor positive trends” in favour of Kevzara, none reached statistical significance and the trial – including a second cohort involving patients being treated with a higher 800mg dose of the antibody – has now been abandoned.
A previous study of 200mg and 400mg doses of the drug in less severely-ill patients also failed to show an impact when it was reported in April, causing Sanofi and Regeneron to refocus their efforts only in those who are considered critically ill with COVID-19.
Furthermore, last month, Roche’s IL-6 inhibitor Actemra/RoActemra (tocilizumab) also failed to show a benefit in an Italian study involving patients with early-stage COVID-19 pneumonia.
Roche’s drug remains in the phase 3 COVACTA trial for more severe coronavirus cases, and is also being tested in combination with Gilead’s remdesivir, which reduced the time to hospital discharge in clinical trials, in the REMDACTA study.
Meanwhile, Sanofi and Regeneron are also running another trial of Kevzara in hospitalised patients with severe and critical COVID-19 using a different dosing regimen. There’s no question however that the latest result further diminishes the prospects for IL-6 inhibitors as a coronavirus therapy.
The hypothesis behind the use of the drugs is that they interfere with a runaway immune system response or ‘cytokine storm’ that develops in the sickest people with COVID-19, leading to acute respiratory distress syndrome (ARDS) as well as damage to other organs.
There was much better news last month after the RECOVERY trial showed that a low dose of cheap steroid dexamethasone – which also dampens down inflammation – was able to reduce the chances of death by around a third in patients requiring mechanical ventilation, and 20% in those needing oxygen support.
Eli Lilly’ JAK inhibitor anti-inflammatory drug Olumiant (baricitinib) – already approved to treat rheumatoid arthritis – is also being tested as a potential treatment for hospitalised COVID-19 in two phase 3 trials.
Hopes that already-approved drugs targeting IL-6 could be repurposed to treat COVID-19 have been undermined by disappointing results from the first large-scale trial of Sanofi and Regeneron’s Kevzara.
The two drugmakers have revealed that adding a 400mg daily dose of Kevzara (sarilumab) to standard care for COVID-19 patients on mechanical ventilation didn’t improve the main outcome goal.
The primary measure in the study was the percentage of those who achieved at least a one-point change from baseline on a seven-point scale, ranging from death to discharge from hospital.
While there were “minor positive trends” in favour of Kevzara, none reached statistical significance and the trial – including a second cohort involving patients being treated with a higher 800mg dose of the antibody – has now been abandoned.
A previous study of 200mg and 400mg doses of the drug in less severely-ill patients also failed to show an impact when it was reported in April, causing Sanofi and Regeneron to refocus their efforts only in those who are considered critically ill with COVID-19.
Furthermore, last month, Roche’s IL-6 inhibitor Actemra/RoActemra (tocilizumab) also failed to show a benefit in an Italian study involving patients with early-stage COVID-19 pneumonia.
Roche’s drug remains in the phase 3 COVACTA trial for more severe coronavirus cases, and is also being tested in combination with Gilead’s remdesivir, which reduced the time to hospital discharge in clinical trials, in the REMDACTA study.
Meanwhile, Sanofi and Regeneron are also running another trial of Kevzara in hospitalised patients with severe and critical COVID-19 using a different dosing regimen. There’s no question however that the latest result further diminishes the prospects for IL-6 inhibitors as a coronavirus therapy.
The hypothesis behind the use of the drugs is that they interfere with a runaway immune system response or ‘cytokine storm’ that develops in the sickest people with COVID-19, leading to acute respiratory distress syndrome (ARDS) as well as damage to other organs.
There was much better news last month after the RECOVERY trial showed that a low dose of cheap steroid dexamethasone – which also dampens down inflammation – was able to reduce the chances of death by around a third in patients requiring mechanical ventilation, and 20% in those needing oxygen support.
Eli Lilly’ JAK inhibitor anti-inflammatory drug Olumiant (baricitinib) – already approved to treat rheumatoid arthritis – is also being tested as a potential treatment for hospitalised COVID-19 in two phase 3 trials.
Recent CYDY News
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 04/08/2026 09:15:18 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 04/08/2026 12:30:28 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 03/25/2026 09:16:10 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:24:23 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:23:14 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:22:42 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:21:33 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:20:57 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:20:20 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/24/2026 09:15:24 PM
- CytoDyn Presents at AACR Special Conference in Cancer Research: Brain Cancer • GlobeNewswire Inc. • 03/24/2026 12:30:00 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 03/09/2026 09:15:18 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/05/2026 01:35:02 PM
- CytoDyn Closes $17.5 Million Financing to Fund Continued Development of Leronlimab • GlobeNewswire Inc. • 03/05/2026 01:30:00 PM
- CytoDyn Presents Novel CCR5 Inhibition Mechanisms and Long-Term Survival Signals for Leronlimab in Metastatic Breast Cancer at AACR Immuno-Oncology Conference • GlobeNewswire Inc. • 02/20/2026 01:30:00 PM
- CytoDyn Announces Funding and Initiation of Expanded Access Program for Patients with Triple-negative Breast Cancer • GlobeNewswire Inc. • 01/27/2026 01:30:00 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 01/09/2026 10:15:22 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 01/09/2026 01:30:45 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 12/22/2025 10:15:23 PM
- Form EFFECT - Notice of Effectiveness • Edgar (US Regulatory) • 12/17/2025 05:15:14 AM
- December 2025 Letter to Shareholders • GlobeNewswire Inc. • 12/16/2025 01:30:00 PM
- Form POS AM - Post-Effective amendments for registration statement • Edgar (US Regulatory) • 12/10/2025 10:16:32 PM
- CytoDyn to Showcase PD-L1 Upregulation and Improved Survival in Metastatic Triple Negative Breast Cancer at the San Antonio Breast Cancer Symposium • GlobeNewswire Inc. • 12/08/2025 01:30:00 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 12/02/2025 10:15:21 PM

