1. Efficacy and safety of an inactivated whole-virion SARS-CoV-2 vaccine (CoronaVac): interim results of a double-blind, randomised, placebo-controlled, phase 3 trial in Turkey
- Author
-
Mine Durusu Tanriover, Hamdi Levent Doğanay, Murat Akova, Hatice Rahmet Güner, Alpay Azap, Sıla Akhan, Şükran Köse, Fatma Şebnem Erdinç, Emin Halis Akalın, Ömer Fehmi Tabak, Hüsnü Pullukçu, Özgür Batum, Serap Şimşek Yavuz, Özge Turhan, Mustafa Taner Yıldırmak, İftihar Köksal, Yeşim Taşova, Volkan Korten, Gürdal Yılmaz, Mustafa Kemal Çelen, Sedat Altın, İlhami Çelik, Yaşar Bayındır, İlkay Karaoğlan, Aydın Yılmaz, Aykut Özkul, Hazal Gür, Serhat Unal, Bircan Kayaaslan, İmran Hasanoğlu, Ayça Dalkıran, Ömer Aydos, Güle Çınar, İrem Akdemir-Kalkan, Ahmet Çağkan İnkaya, Mehtap Aydin, Hatice Çakir, Jale Yıldız, Özenir Kocabıyık, Sonay Arslan, Bayram Nallı, Ömer Demir, Sarp Singil, Çiğdem Ataman-Hatipoğlu, Günay Tuncer-Ertem, Sami Kınıklı, Uğur Önal, Bilgül Mete, Gözde Dalgan, Meltem Taşbakan, Tansu Yamazhan, Berna Kömürcüoğlu, Enver Yalnız, Aysun Benli, Çağla Keskin-Sarıtaş, Mustafa Gökhan Ertosun, Özlenen Özkan, Salih Emre, Seçil Arıca, Ferit Kuşçu, Aslıhan Candevir, Buket Ertürk-Şengel, Fadime Ayvaz, Firdevs Aksoy, Çiğdem Mermutluoğlu, Yakup Demir, Gülşah Günlüoğlu, Seda Tural-Önür, Ayşin Kılıç-Toker, Esma Eren, Barış Otlu, Ayşe Özlem Mete, Kübra Koçak, Hale Ateş, İlkay Koca-Kalkan, Kurtuluş Aksu, and Acibadem University Dspace
- Subjects
medicine.medical_specialty ,education.field_of_study ,business.industry ,Population ,Administrative Personnel ,General Medicine ,Articles ,Placebo ,Vaccine efficacy ,Antibodies, Viral ,Antibodies, Neutralizing ,law.invention ,Clinical trial ,Vaccination ,Randomized controlled trial ,Tolerability ,law ,Internal medicine ,Cohort ,medicine ,Humans ,education ,business - Abstract
Background CoronaVac, an inactivated whole-virion SARS-CoV-2 vaccine, has been shown to be well tolerated with a good safety profile in individuals aged 18 years and older in phase 1/2 trials, and provided a good humoral response against SARS-CoV-2. We present the interim efficacy and safety results of a phase 3 clinical trial of CoronaVac in Turkey. Methods This was a double-blind, randomised, placebo-controlled phase 3 trial. Volunteers aged 18-59 years with no history of COVID-19 and with negative PCR and antibody test results for SARS-CoV-2 were enrolled at 24 centres in Turkey. Exclusion criteria included (but were not limited to) immunosuppressive therapy (including steroids) within the past 6 months, bleeding disorders, asplenia, and receipt of any blood products or immunoglobulins within the past 3 months. The K1 cohort consisted of health-care workers (randomised in a 1:1 ratio), and individuals other than health-care workers were also recruited into the K2 cohort (randomised in a 2:1 ratio) using an interactive web response system. The study vaccine was 3 mu g inactivated SARS-CoV-2 virion adsorbed to aluminium hydroxide in a 0.5 mL aqueous suspension. Participants received either vaccine or placebo (consisting of all vaccine components except inactivated virus) intramuscularly on days 0 and 14. The primary efficacy outcome was the prevention of PCR-confirmed symptomatic COVID-19 at least 14 days after the second dose in the per protocol population. Safety analyses were done in the intention-to-treat population. This study is registered with ClinicalTrials.gov (NCT04582344) and is active but no longer recruiting. Findings Among 11 303 volunteers screened between Sept 14, 2020, and Jan 5, 2021, 10 218 were randomly allocated. After exclusion of four participants from the vaccine group because of protocol deviations, the intention-to-treat group consisted of 10 214 participants (6646 [65.1%] in the vaccine group and 3568 [34.9%] in the placebo group) and the per protocol group consisted of 10 029 participants (6559 [65.4%] and 3470 [34.6%]) who received two doses of vaccine or placebo. During a median follow-up period of 43 days (IQR 36-48), nine cases of PCR-confirmed symptomatic COVID-19 were reported in the vaccine group (31.7 cases [14.6-59.3] per 1000 person-years) and 32 cases were reported in the placebo group (192.3 cases [135.7-261.1] per 1000 person-years) 14 days or more after the second dose, yielding a vaccine efficacy of 83.5% (95% CI 65.4-92.1; p, TUSEB, We are grateful to all participants who volunteered to be part of this study and to all members of the clinical research teams of the participating sites. We thank TUSEB for funding the study and Omega-CRO for the statistical analyses and production of figures, and providing the study protocol. We also thank the members of the data and safety monitoring board for their contributions in the safe execution of this study.
- Published
- 2021