Treatment of Middle East Respiratory Syndrome with a combination of lopinavir-ritonavir and interferon-[beta]1b : study protocol for a randomized controlled trial

• Published in: Trials 2018-01, Vol.19 (1)
• Main Authors: Arabi, Yaseen M, Alothman, Adel, Balkhy, Hanan H, Al-Dawood, Abdulaziz, AlJohani, Sameera, Al Harbi, Shmeylan, Kojan, Suleiman, Al Jeraisy, Majed, Deeb, Ahmad M, Assiri, Abdullah M, Al-Hameed, Fahad, AlSaedi, Asim, Mandourah, Yasser, Almekhlafi, Ghaleb A, Sherbeeni, Nisreen Murad, Elzein, Fatehi Elnour, Memon, Javed, Taha, Yusri, Almotairi, Abdullah, Maghrabi, Khalid A, Qushmaq, Ismael, Al Bshabshe, Ali, Kharaba, Ayman, Shalhoub, Sarah, Jose, Jesna, Fowler, Robert A, Hayden, Frederick G, Hussein, Mohamed A,
• Format: Article
• Language: English
• Subjects: Comparative analysis; Complications and side effects; Dosage and administration; Drug therapy; Health aspects; Interferon beta; Lopinavir; Middle East respiratory syndrome; Ritonavir
• ISSN: 1745-6215; 1745-6215
• DOI: 10.1186/s13063-017-2427-0

Background It had been more than 5 years since the first case of Middle East Respiratory Syndrome coronavirus infection (MERS-CoV) was recorded, but no specific treatment has been investigated in randomized clinical trials. Results from in vitro and animal studies suggest that a combination of lopinavir/ritonavir and interferon-[beta]1b (IFN-[beta]1b) may be effective against MERS-CoV. The aim of this study is to investigate the efficacy of treatment with a combination of lopinavir/ritonavir and recombinant IFN-[beta]1b provided with standard supportive care, compared to treatment with placebo provided with standard supportive care in patients with laboratory-confirmed MERS requiring hospital admission. Methods The protocol is prepared in accordance with the SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) guidelines. Hospitalized adult patients with laboratory-confirmed MERS will be enrolled in this recursive, two-stage, group sequential, multicenter, placebo-controlled, double-blind randomized controlled trial. The trial is initially designed to include 2 two-stage components. The first two-stage component is designed to adjust sample size and determine futility stopping, but not efficacy stopping. The second two-stage component is designed to determine efficacy stopping and possibly readjustment of sample size. The primary outcome is 90-day mortality. Discussion This will be the first randomized controlled trial of a potential treatment for MERS. The study is sponsored by King Abdullah International Medical Research Center, Riyadh, Saudi Arabia. Enrollment for this study began in November 2016, and has enrolled thirteen patients as of Jan 24-2018. Trial registration ClinicalTrials.gov, ID: NCT02845843. Registered on 27 July 2016. Keywords: Coronavirus, MERS, Antiviral, Saudi Arabia, Clinical trial, Lopinavir/ritonavir, Interferon-[beta]1b