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Rapid Experimental Medicine for COVID-19 (DEFINE)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04473053
Recruitment Status : Recruiting
First Posted : July 16, 2020
Last Update Posted : August 21, 2020
Sponsor:
Collaborators:
University of Oxford
Latus Therapeutics
Information provided by (Responsible Party):
University of Edinburgh

Brief Summary:

COVID-19 is a community acquired pneumonia caused by infection with a novel coronavirus, SARS CoV2 and is a serious condition with high mortality in hospitalised patients, for which there is no currently approved treatment other than supportive care. Urgent investigation of potential treatments for this condition is required.

This protocol describes an overarching and adaptive trial designed to provide safety, pharmacokinetic (PK)/ pharmacodynamic (PD) information and exploratory biological surrogates of efficacy which may support further development and deployment of candidate therapies in larger scale trials of COVID-19 positive patients receiving normal standard of care.

Given the spectrum of clinical disease, community based infected patients or hospitalised patients can be included. Products requiring parenteral administration will only be investigated in hospitalised patients. Patients will be divided into cohorts, a) community b) hospitalised patients with new changes on a chest x-ray (CXR) or a computed tomography (CT) scan or requiring supplemental oxygen and c) hospitalised requiring assisted ventilation. Participants may be recruited from all three of these cohorts, depending on the experimental therapy, its route of administration and mechanism of action. The relevant cohort(s) for any given therapy will be detailed in the therapy-specific appendix.

Candidate therapies can be added to the protocol and previous candidates removed from further investigation as evidence emerges. The trial will be monitored by an independent Data Monitoring Committee (DMC) to ensure patient safety.

Each candidate cohort will include a small cohort of patients randomised to candidate therapy or existing standard of care management dependent on disease stage at entry. Cohort numbers will be defined in the protocol appendices.

This is a Phase IIa experimental medicine trial and as such formal sample size calculations are not appropriate.


Condition or disease Intervention/treatment Phase
COVID-19 Drug: Nafamostat Mesilate Drug: TD139 Other: Standard care Phase 2 Phase 3

Detailed Description:

This trial platform aims to support the repurposing of promising therapeutic assets with prior use in humans but without prior information on use in COVID-19, to determine the PK-PD profile of the agent, compared to standard of care supportive therapy, in small cohorts of COVID-19 patients. The results of these studies are intended to provide initial safety, pharmacokinetic and pharmacodynamic data and experimental medicine data to support further evaluation in existing national and international trial networks for candidates demonstrating appropriate impact on the dynamic marker of interest. The key interception is to mitigate the lung damage in patients with COVID-19 that leads to respiratory failure. As such, the assets in this programme will focus on abrogating putative mechanisms implicated in COVID-19 respiratory disease.

Existing approaches in clinical trials involve novel or repurposed antivirals or immunomodulatory approaches involving agents such as corticosteroids, interferon-β or hydroxychloroquine. A major limitation in the design of many early clinical trials is the limited amount of mechanistic data from patients with COVID-19. Mechanisms have been inferred from animal models, related infections or clinical syndromes. These approaches have infrequently translated to human disease. For example, remdesivir efficacy in animal models of Ebola Virus Disease (EVD) did not translate to human disease and hydroxychloroquine antiviral affects in vitro have not translated to humans against other viruses. Some drugs, such as repurposing of the anti-retroviral protease Kaletra, are still being pursued despite uncertain mechanism and despite evidence that this aspartyl protease cannot bind to the cysteine chymotrypsin-like protease that is Kaletra's putative target in COVID-19.

There is a clear and urgent need to pursue experimental medicine studies in humans to establish a solid mechanistic basis for rapid evaluation, including in existing clinical trial platforms against COVID-19 (e.g DoH RECOVERY and NIHR-CLRN industry adopted studies).

The trial will be as flexible as possible to ensure a broad range of patients can be recruited and candidate therapies can be added or removed as evidence emerges. The interim trial results will be monitored by an independent DMC to evaluate any patient safety signals.

As COVID-19 follows a variable clinical path in individual patients, the protocol is designed to enable inclusion of patients across the disease stages. The trial is intended to provide mechanistic data from patients receiving standard of care therapy and from patients treated with the therapy candidates. The study will enable delivery of pharmacokinetic information and effects of standard of care and candidate agents on surrogate biomarkers of the disease process and the specific drug target.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 60 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Randomised clinical trial - currently two treatment arms and one standard of care arm
Masking: Single (Outcomes Assessor)
Masking Description: The biomarker analysis team will be masked to the trial treatment.
Primary Purpose: Treatment
Official Title: Rapid Experimental Medicine for COVID-19 - DEFINE COVID-19
Actual Study Start Date : July 3, 2020
Estimated Primary Completion Date : July 3, 2021
Estimated Study Completion Date : December 3, 2021

Arm Intervention/treatment
Experimental: Nafamostat
It is intended that the licensed dose (0.2mg/kg/hr) in Japan will be used. Patients randomised to Nafamostat will receive a continuous intravenous infusion at 0.2 mg/kg/hr for 7 days. If a participant is discharged from hospital or can no longer receive this treatment, the treatment will be stopped.
Drug: Nafamostat Mesilate
Nafamostat has been shown to have potential antiviral effects against MERS CoV and is thought to possibly inhibit SARS CoV2 infection via inhibition of viral entry due to inhibition of TMPRSS2. In addition, nafamostat has potent anticoagulant properties which may provide benefit in patients with DIC, a common finding in serious cases of COVID-19. Nafamostat has been broadly well tolerated in clinical trials in patients with DIC and acute pancreatitis.

Experimental: TD139

Patients will inhale 5mg x 2 (10 mg) twice daily for the first 48 hrs and then subsequently 5mg x 2 (10 mg) once daily for the remaining 12 days. Unless a participant is discharged from hospital or can no longer use an inhaler - in which case treatment will be stopped at such time.

CE marked inhalers will be provided by the Manufacturer. All patients will receive guidance on how to use the inhaler by an appropriately trained member of the research team. Two individual inhalers will be used by each patient over the course of the 14 day study period (each inhaler will be used by one patient for 7 days) and will be thoroughly cleaned with an antiseptic wipe before and after each use.

Drug: TD139
TD139 is a specific inhibitor of galectin-3 which has been investigated in healthy volunteers and patients with IPF. No serious drug related serious adverse events have been reported to date. TD139 had no impact on cardiac, haematological or biochemical measures of safety during trials in humans to date. Beneficial effects on biomarker measures of lung inflammation were observed in patients with IPF. It is the purpose of this investigation to examine the potential for delivery of this inhibitor in pre-ventilator patients hospitalised with COVID-19 to examine whether this may lead to detectable changes in blood biomarkers, reduce viral load and also reduce disease severity such as time to ventilation.

Active Comparator: Standard of Care
All treatment arms will be compared to the Standard of Care arm.
Other: Standard care
Patients will receive standard care.




Primary Outcome Measures :
  1. The safety of the candidate therapies in COVID-19 patients by measuring physiological changes in the circulatory and respiratory system. [ Time Frame: Up to 16 days post treatment ]
    Measure vital signs (blood pressure/heart rate/temperature and respiratory rate)

  2. The safety of the candidate therapies in COVID-19 patients by recording the number of treatment related adverse events. [ Time Frame: Up to 90 days post treatment ]
    Record number of participants With treatment-related adverse events


Secondary Outcome Measures :
  1. Measuring the PK of the proposed trial treatments in COVID-19 patients. [ Time Frame: 6 months ]
    Measure maximum plasma concentration [Cmax] in blood samples.

  2. Measure a change in the expression of key coagulation biomarkers in the blood of COVID-19 patients during and after treatment period. [ Time Frame: 6 months ]
    Change in expression or activity of coagulation markers in serial blood samples taken before, during and after treatment.

  3. Measure a change in the expression of key cytokines in the blood of COVID-19 patients during and after treatment period. [ Time Frame: 6 months ]
    Change in expression or activity of inflammatory cytokines in serial blood samples taken before, during and after treatment.

  4. To evaluate the improvement or deteroriation of patients in each treatment arm. [ Time Frame: 16 days ]
    Record changes in National Early Warning Score (NEWS) 2 score. Scale is from 0-20, with a higher number indicating a higher risk of morbidity.

  5. To evaluate the number of oxygen-free days. [ Time Frame: 16 days ]
    Duration (days) of oxygen use

  6. To evaluate incidence of any form of new ventilation use. [ Time Frame: 16 days ]
    Duration (days) of ventilation

  7. To evaluate ventilator-free days [ Time Frame: 16 days ]

    Duration of ventilation-free days.

    • Incidence of any form of new ventilation use and duration (days) of new ventilation use.


  8. Change in the ratio of the oxygen saturation to fraction of inspired oxygen concentration (SpO2/FiO2) [ Time Frame: 16 days ]
    SpO2/FiO2, measured daily from randomisation to Day 15, hospital discharge, or death

  9. To evaluate SARS-CoV-2 viral load. [ Time Frame: 15 days ]
    Qualitative and quantitative polymerase chain reaction (PCR) determination of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in oropharyngeal/nasal/saliva swab while hospitalised on Days 1, 3, 5, 8, 11, 15.

  10. To evaluate time to discharge [ Time Frame: 16 days ]

    Duration of total hospital stay

    • Duration to discharge following treatment


  11. To evaluate the use of renal dialysis or haemofiltration for each treatment arm. [ Time Frame: 16 days ]
    Record requirement for renal dialysis or haemofiltration



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   16 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Provision of informed consent from the patient or representative
  • Aged at least 16 years
  • If the patient is of child bearing potential, the patient, and their partner(s), agree to use medically-accepted double-barrier methods of contraception (eg, barrier methods, including male condom, female condom or diaphragm with spermicidal gel) during the study (if randomised to a treatment arm) and for at least 90 days after termination of study therapy. A vasectomised partner would be considered an appropriate birth control method provided that the partner is the sole male sexual partner and the absence of sperm has been confirmed.
  • COVID-19 positive

Exclusion Criteria:

  • Current or recent history, as determined by the Investigator, of severe, progressive, and/or uncontrolled cardiac disease (NYHA class IV), uncontrolled renal disease (eGFR <30 mL/min/1.73 m2), severe liver dysfunction (ALT/AST >5x ULN) or bone marrow failure (Hb <80 g/L AND ANC<0.5 mm3 AND platelet count <50,000 uL)
  • Women who are pregnant or breastfeeding.
  • Participation in another clinical trial of an investigational medicinal product (CTIMP)
  • Known hypersensitivity to the IMP or excipients (e.g. lactose)
  • Pre-existing or Cconcomittant use of off-label treatments for COVID-19 that are not recognised as locally approved standard care.
  • Significant electrolyte disturbance (hyperkalaemia potassium >5.0 mmol/L or hyponatraemia sodium < 120mmol/L)
  • Patient currently receiving potassium sparing diuretics that cannot be reasonably withheld
  • Patient currently receiving prophylactic or therapeutic anticoagulantsanticoagulation or antiplatelet agents that cannot be reasonably withheld if randomised to Nafamostat
  • Patients (or their partners) planning on donating sperm/eggs during the trial period
  • Ongoing dialysis
  • History of serious liver disease (Child Pugh score > 10)
  • Hemoglobin < 80 g/L
  • Any known allergy to the IMP/excipients
  • Severe uncontrolled diabetes mellitus
  • In the Investigator's opinion, patient is unwilling or unable to comply with drug administration plan, laboratory tests or other study procedures.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04473053


Contacts
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Contact: Annya Bruce, PhD 01312429180 Annya.Bruce@ed.ac.uk
Contact: Kevin Dhaliwal 01312429180 kev.dhaliwal@ed.ac.uk

Locations
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United Kingdom
NHS Lothian Recruiting
Edinburgh, United Kingdom, EH16 4TJ
Contact: Kev Dhaliwal    01312426579    Kev.Dhaliwal@ed.ac.uk   
Contact: Annya Bruce    01312429180    Annya.Bruce@ed.ac.uk   
Sponsors and Collaborators
University of Edinburgh
University of Oxford
Latus Therapeutics
Investigators
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Principal Investigator: Kev Dhaliwal University of Edinburgh
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Responsible Party: University of Edinburgh
ClinicalTrials.gov Identifier: NCT04473053    
Other Study ID Numbers: AC20063
First Posted: July 16, 2020    Key Record Dates
Last Update Posted: August 21, 2020
Last Verified: August 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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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
Additional relevant MeSH terms:
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Nafamostat
Anti-Inflammatory Agents, Non-Steroidal
Analgesics, Non-Narcotic
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Anti-Inflammatory Agents
Antirheumatic Agents
Anticoagulants
Protease Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Trypsin Inhibitors
Serine Proteinase Inhibitors
Complement Inactivating Agents
Immunosuppressive Agents
Immunologic Factors