Randomised Evaluation of COVID-19 Therapy (RECOVERY)

• ClinicalTrials.gov Identifier: NCT04381936
• Recruitment Status: Recruiting
• First Posted: May 11, 2020
• Last Update Posted: June 5, 2020
• Sponsor: University of Oxford
• Collaborators: UK Research and Innovation; National Institute for Health Research, United Kingdom; Wellcome; Bill and Melinda Gates Foundation; Department for International Development, United Kingdom; Health Data Research UK; Medical Research Council Population Health Research Unit; NIHR Clinical Trials Unit Support Funding
• Information provided by (Responsible Party): University of Oxford

Tracking Information

• First Submitted Date: May 7, 2020
• First Posted Date: May 11, 2020
• Last Update Posted Date: June 5, 2020
• Actual Study Start Date: March 19, 2020
• Estimated Primary Completion Date: December 2020 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: May 7, 2020)

All-cause mortality [ Time Frame: Within 28 days after randomisation ]

For each pairwise comparison with the 'no additional treatment' arm, the primary objective is to provide reliable estimates of the effect of study treatments on all-cause mortality.

• Original Primary Outcome Measures: Same as current

Current Secondary Outcome Measures (submitted: June 3, 2020)

• Duration of hospital stay [ Time Frame: Within 28 days and up to 6 months after the main randomisation ]
  To assess the effects of study treatment on number of days stay in hospital
• Need for (and duration of) ventilation [ Time Frame: Within 28 days and up to 6 months after the main randomisation ]
  To assess the effects of study treatment on number of patients who needed ventilation and the number of days it was required
• Composite endpoint of death or need for mechanical ventilation or ECMO [ Time Frame: Within 28 days and up to 6 months after the main randomisation ]
  Among patients not on ventilation at baseline, the number of patients with a composite endpoint of death or need for mechanical ventilation or ECMO.

Original Secondary Outcome Measures (submitted: May 7, 2020)

• Duration of hospital stay [ Time Frame: Within 28 days after randomisation ]
  To assess the effects of study treatment on number of days stay in hospital
• Need for (and duration of) ventilation [ Time Frame: Within 28 days after randomisation ]
  To assess the effects of study treatment on number of patients who needed ventilation and the number of days it was required
• Need for renal replacement [ Time Frame: Within 28 days after randomisation ]
  To assess the effects of study treatment on number of patients who needed renal replacement therapy

Current Other Pre-specified Outcome Measures (submitted: June 3, 2020)

• Need for renal replacement [ Time Frame: Within 28 days and up to 6 months after the main randomisation ]
  To assess the effects of study treatment on number of patients who needed renal replacement therapy
• Development of new major cardiac arrythmias [ Time Frame: Within 28 days and up to 6 months after the main randomisation ]
  To assess the effects of study treatment on number of patients who develop new major cardiac arrythmias

• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Randomised Evaluation of COVID-19 Therapy
• Official Title: Randomised Evaluation of COVID-19 Therapy
• Brief Summary: RECOVERY is a randomised trial investigating whether treatment with either Lopinavir-Ritonavir, Hydroxychloroquine, Corticosteroids, Azithromycin, Convalescent plasma or Tocilizumab prevents death in patients with COVID-19.

Detailed Description

BACKGROUND: In early 2020, as this protocol was being developed, there were no approved treatments for COVID-19, a disease induced by the novel coronavirus SARSCoV-2 that emerged in China in late 2019. The UK New and Emerging Respiratory Virus Threats Advisory Group (NERVTAG) advised that several possible treatments should be evaluated, including Lopinavir-Ritonavir, low-dose corticosteroids, and Hydroxychloroquine. These groups also advised that other treatments will soon emerge that require evaluation. A World Health Organization (WHO) expert group issued broadly similar advice.

ELIGIBILITY AND RANDOMISATION: This protocol describes a randomised trial among patients hospitalised for COVID-19. All eligible patients are randomly allocated between several treatment arms, each to be given in addition to the usual standard of care in the participating hospital: No additional treatment vs Lopinavir-Ritonavir vs Low-dose Corticosteroids vs Hydroxychloroquine vs Azithromycin. In a factorial design, eligible patients are allocated simultaneously to no additional treatment vs convalescent plasma. The study allows a subsequent randomisation for patients with progressive COVID-19 (evidence of hyper-inflammatory state): No additional treatment vs Tocilizumab. For patients for whom not all the trial arms are appropriate or at locations where not all are available, randomisation will be between fewer arms.

ADAPTIVE DESIGN: The interim trial results will be monitored by an independent Data Monitoring Committee (DMC). The most important task for the DMC will be to assess whether the randomised comparisons in the study have provided evidence on mortality that is strong enough (with a range of uncertainty around the results that is narrow enough) to affect national and global treatment strategies. In such a circumstance, the DMC will inform the Trial Steering Committee who will make the results available to the public and amend the trial arms accordingly. New trial arms can be added as evidence emerges that other candidate therapeutics should be evaluated.

OUTCOMES: The main outcomes will be death, discharge, need for ventilation and need for renal replacement therapy. For the main analyses, follow-up will be censored at 28 days after randomisation. Additional information on longer term outcomes may be collected through review of medical records or linkage to medical databases such as those managed by NHS Digital and equivalent organisations in the devolved nations.

SIMPLICITY OF PROCEDURES: To facilitate collaboration, even in hospitals that suddenly become overloaded, patient enrolment (via the internet) and all other trial procedures are greatly streamlined. Informed consent is simple and data entry is minimal. Randomisation via the internet is simple and quick, at the end of which the allocated treatment is displayed on the screen and can be printed or downloaded. Follow-up information is recorded at a single timepoint and may be ascertained by contacting participants in person, by phone or electronically, or by review of medical records and databases.

DATA TO BE RECORDED: At randomisation, information will be collected on the identity of the randomising clinician and of the patient, age, sex, major co-morbidity, pregnancy, COVID-19 onset date and severity, and any contraindications to the study treatments. The main outcomes will be death (with date and probable cause), discharge (with date), need for ventilation (with number of days recorded) and need for renal replacement therapy. Reminders will be sent if outcome data have not been recorded by 28 days after randomisation. Suspected Unexpected Serious Adverse Reactions (SUSARs) to one of the study medication (eg, Stevens-Johnson syndrome, anaphylaxis, aplastic anaemia) will be collected and reported in an expedited fashion. Other adverse events will not be recorded but may be available through linkage to medical databases.

NUMBERS TO BE RANDOMISED: The larger the number randomised the more accurate the results will be, but the numbers that can be randomised will depend critically on how large the epidemic becomes. If substantial numbers are hospitalised in the participating centres then it may be possible to randomise several thousand with mild disease and a few thousand with severe disease, but realistic, appropriate sample sizes could not be estimated at the start of the trial.

HETEROGENEITY BETWEEN POPULATIONS: If sufficient numbers are studied, it may be possible to generate reliable evidence in certain patient groups (e.g. those with major comorbidity or who are older). To this end, data from this study may be combined with data from other trials of treatments for COVID-19, such as those being planned by the WHO.

ADD-ON STUDIES: Particular countries or groups of hospitals, may well want to collaborate in adding further measurements or observations, such as serial virology, serial blood gases or chemistry, serial lung imaging, or serial documentation of other aspects of disease status. While well-organised additional research studies of the natural history of the disease or of the effects of the trial treatments could well be valuable (although the lack of placebo control may bias the assessment of subjective side-effects, such as gastrointestinal problems), they are not core requirements.

• Study Type: Interventional
• Study Phase: Phase 2; Phase 3

Study Design

Allocation: Randomized
Intervention Model: Factorial Assignment
Intervention Model Description:

Main randomisation (part A): Eligible patients will be randomly allocated between the available 5 treatment arms.

Main randomisation (part B): Simultaneously, eligible patients will be randomly allocated between convalescent plasma or no additional treatment.

Subsequent randomisation: Participants with progressive COVID-19 (as evidenced by hypoxia and an inflammatory state) may undergo an optional second randomisation.

Masking: None (Open Label)
Primary Purpose: Treatment

• Condition: Severe Acute Respiratory Syndrome

Intervention

• Drug: Lopinavir-Ritonavir
  Lopinavir 400mg-Ritonavir 100mg by mouth (or nasogastric tube) every 12 hours for 10 days.
• Drug: Corticosteroid
  Corticosteroid in the form of dexamethasone administered as an oral (liquid or tablets) or intravenous preparation 6 mg once daily for 10 days. In pregnancy or breastfeeding women, prednisolone 40 mg administered by mouth (or intravenous hydrocortisone 80 mg twice daily) should be used instead of dexamethasone.
• Drug: Hydroxychloroquine
  Hydroxychloroquine by mouth for a total of 10 days (see Protocol for timing and dosage).
• Drug: Azithromycin
  Azithromycin 500mg by mouth (or nasogastric tube) or intravenously once daily for 10 days.
• Biological: Convalescent plasma
  Single unit of ABO compatible convalescent plasma (275mls +/- 75 mls) intravenous per day on study days 1 (as soon as possible after randomisation) and 2 (with a minimum of 12 hour interval between 1st and 2nd units).
• Drug: Tocilizumab
  Tocilizumab by intravenous infusion with the dose determined by body weight (see Protocol for dosage)

Study Arms

• No Intervention: Standard Care
  Patient receives usual hospital care
• Active Comparator: Low dose corticosteroids
  First (main) randomisation part A
  Intervention: Drug: Corticosteroid
• Active Comparator: Hydroxychloroquine
  First (main) randomisation part A
  Intervention: Drug: Hydroxychloroquine
• Active Comparator: Lopinavir-Ritonavir
  First (main) randomisation part A
  Intervention: Drug: Lopinavir-Ritonavir
• Active Comparator: Azithromycin
  First (main) randomisation part A
  Intervention: Drug: Azithromycin
• Active Comparator: Convalescent plasma
  First (main) randomisation part B
  Intervention: Biological: Convalescent plasma
• Active Comparator: Tocilizumab
  Participants with progressive COVID-19 (as evidenced by hypoxia and an inflammatory state) may undergo an optional subsequent randomisation between Tocilizumab and no additional treatment.
  Intervention: Drug: Tocilizumab

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Recruiting
• Estimated Enrollment (submitted: May 7, 2020): 12000
• Original Estimated Enrollment: Same as current
• Estimated Study Completion Date: June 2021
• Estimated Primary Completion Date: December 2020 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• (i) Hospitalised
• (ii) SARS-CoV-2 infection (clinically suspected or laboratory confirmed)
• (iii) No medical history that might, in the opinion of the attending clinician, put the patient at significant risk if he/she were to participate in the trial

Exclusion Criteria:

• If the attending clinician believes that there is a specific contra-indication to one of the active drug treatment arms (see Protocol Appendix 2; section 8.2 and Appendix 3; section 8.3 for children) or that the patient should definitely be receiving one of the active drug treatment arms then that arm will not be available for randomisation for that patient. For patients who lack capacity, an advanced directive or behaviour that clearly indicates that they would not wish to participate in the trial would be considered sufficient reason to exclude them from the trial.

Sex/Gender

• Sexes Eligible for Study: All

• Ages: Child, Adult, Older Adult
• Accepts Healthy Volunteers: No

Contacts

Contact: Richard Haynes; +44 (0)1865 743743; recoverytrial@ndph.ox.ac.uk

• Listed Location Countries: United Kingdom

Administrative Information

• NCT Number: NCT04381936
• Other Study ID Numbers: NDPHRECOVERY; 2020-001113-21 ( EudraCT Number ); ISRCTN50189673 ( Registry Identifier: ISRCTN )
• Has Data Monitoring Committee: Yes

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Product Manufactured in and Exported from the U.S.: No

IPD Sharing Statement

• Plan to Share IPD: Yes
• Plan Description: The data-sharing plans for this study will be made available at a later date.
• Supporting Materials: Study Protocol
• Supporting Materials: Statistical Analysis Plan (SAP)
• Supporting Materials: Informed Consent Form (ICF)
• Access Criteria: Proposals for substudies must be approved by the Trial Steering Committee. Procedures for accessing the data for this study are available on https://www.ndph.ox.ac.uk/data-access
• URL: https://www.ndph.ox.ac.uk/data-access

• Responsible Party: University of Oxford
• Study Sponsor: University of Oxford

Collaborators

• UK Research and Innovation
• National Institute for Health Research, United Kingdom
• Wellcome
• Bill and Melinda Gates Foundation
• Department for International Development, United Kingdom
• Health Data Research UK
• Medical Research Council Population Health Research Unit
• NIHR Clinical Trials Unit Support Funding

Investigators

• Principal Investigator: Peter W Horby; University of Oxford

• PRS Account: University of Oxford
• Verification Date: June 2020