Enoxaparin in COVID-19 Moderate to Severe Hospitalized Patients (INHIXACOV19)

June 15, 2020 updated by: Pierluigi Viale, IRCCS Azienda Ospedaliero-Universitaria di Bologna

Intermediate Dose Enoxaparin in Hospitalized Patients With Moderate-severe COVID19: A Pilot Phase II Single-arm Study, INHIXACOVID19

General objective of the study To assess the efficacy and safety of enoxaparin in hospitalized patients with moderate to severe COVID-19 (Coronavirus Disease 2019) infection.

Study Design

The study consists of two parts:

  • a phase II single-arm interventional prospective study including all patients treated with the study drug;
  • an observational prospective cohort study including all patients screened for receiving the study drug but not included in the phase II study.

Patients will be enrolled from "date of study approval" for 1 month. Each patient will be followed-up for a minimum of 90 days after COVID19 diagnosis.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

General objective of the study To assess the efficacy and safety of enoxaparin in hospitalized patients with moderate to severe COVID-19 infection.

Specific objectives Primary Endpoints To investigate the efficacy of enoxaparin in improving the clinical outcome of hospitalized patients with moderate to severe COVID-19.

  • All-cause in-hospital, 30-day and 90-day mortality rates.
  • Evolution of the clinical severity during treatment.
  • ICU admission and length of ICU stay.
  • Length of hospital stay.

Secondary Endpoints To analyse the safety of enoxaparin in hospitalized patients with with moderate to severe COVID-19.

  • Rate of adverse events (AEs) during treatment, at the end of treatment (EOT) and at 30 days after EOT.
  • Severity of AEs classified according to common terminology criteria for adverse events (CTCAE). The worst degree ever suffered will be considered.

To describe the rates and the types of thromboembolic events among hospitalized patients with confirmed diagnosis of COVID-19.

  • Occurrence of thromboembolic event at 90 days after COVID-19 diagnosis.
  • Description of the type, distribution and severity of thromboembolic events.

Study Design Overall Design

The study consists of two parts:

  • a phase II single-arm interventional prospective study including all patients treated with the study drug;
  • an observational prospective cohort study including all patients screened for receiving the study drug but not included in the phase II study.

Patients will be enrolled from "date of study approval" for 1 month. Each patient will be followed-up for a minimum of 90 days after COVID19 diagnosis.

End of Study Definition A participant is considered to have completed the study if he/she has completed the last scheduled procedure shown in the Schedule of assessments. The end of the study is defined as the date of the last scheduled procedure shown in the Schedule of assessments for the last participant in the trial.

Study Population

Definitions

Clinical severity of COVID-19 will be assessed at the diagnosis of COVID19, during the treatment with the study drug, and at the end of treatment according to the following criteria (1):

  • Mild patients: only show mild symptoms without radiographic features
  • Moderate patients: have fever, respiratory symptoms, and radiographic signs of pneumonia
  • Severe patients: have fever, respiratory symptoms, and radiographic signs of pneumonia plus at least one of three criteria: (1) RR (respiratory rate) >30 times/min, (2) oxygen saturation <93% on ambient air, (3) PaO2/FiO2 (Oxigen partial pressure/inspired oxygen fraction ) <300 mmHg.
  • Critical patients: meet one of three criteria: (1) respiratory failure needing invasive ventilation, (2) septic shock, (3) multiple organ failure.

Major bleeding will be defined according to the ISTH (International Society of Thrombosis and Haemostasis) criteria as one of the following:

  • Fatal bleeding
  • Symptomatic bleeding in a critical area or organ, such as intracranial, intraspinal, intraocular, retroperitoneal, intra-articular or pericardial, or intramuscular with compartment syndrome
  • Bleeding causing a fall in haemoglobin level of 2 g/dL or more, or leading to transfusion of two or more units of whole blood or red cells (11).

Treatments Administration and monitoring of study drug

All patients screened for being included in the study will receive standard thrombo-prophylaxis with LMWH (low molecular weight heparin) (e.g. enoxaparin 40 mg/die). Patients included in the observational cohort will continue on standard thrombo-prophylaxis, while patients included in the interventional study will receive subcutaneous enoxaparin in a single daily dose of:

  • 60 mg once daily in case of body weight of 45 to 60 kg
  • 80 mg per day in case of weight from 61 to 100 kg or
  • 100 mg once daily in case of bodyweight >100 kg Enoxaparin will be started on the first day of COVID19 diagnosis and continued for 14 days, after determination of baseline PT (prothrombin time), aPTT (activated partial thromboplastin time), complete blood cell count and creatinine levels.

After reaching the steady state (usually after the third dose), heparin levels will be measured with the determination of anti-Xa activity on a blood sample obtained at 4 hours after the morning injection. LMWH dose may be then increased or reduced on the basis of target anti-Xa activity (0.4-0.6 antiFXa (Anti Factor X activated) UI/ml (International Unit/ml) for intermediate doses). The determination of anti-Xa activity will be repeated on the fifth or sixth day to monitor any drug accumulation.

Complete blood cell count will be obtained every second day to monitor for heparin induced thrombocytopenia.

Single low dose antiplatelet agents will be allowed. In all patients, RT-PCR (reverse transcription-polymerase chain reaction) nasopharyngeal swabs will be performed every 7 days to assess virus clearance and blood samples will be collected at baseline and on day 7 and will be retrospectively analysed to measure viral load.

Follow up procedures Patients will be followed-up to 90 days after study drug initiation. Follow-up information will be collected via telephone calls, patient medical records and/or clinical visits according to clinical evolution.

This is a pilot study and an initial sample of 100 patients for the phase II single-arm interventional trial is established. Even if currently precise data are not available, it can be assumed that the composite endpoint is around 30% in patient treated with the standard thromboprophylaxis dose of enoxaparin. To verify the hypothesis that the experimental treatment may produce a halving of this endpoint (from 30% to 15%), 300 patients (200 for the observational cohort and 100 for the phase II cohort; ratio 2:1) are needed with a 80% power and a 0,05 bilateral alpha error. As stated above a first safety analysis after enrolling the first 50 patients in the interventional study arm is planned and it will be done by an independent committee. According to safety and efficacy data obtained, using as control the observational cohort, a large study with a more robust design is planned.

Study Type

Interventional

Enrollment (Anticipated)

300

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • Italy
      • Brescia, Italy
      • Brescia, Italy
        • Not yet recruiting
        • Piazzale Spedali Civili, 1, 25123 Brescia BS Medicina Interna UniBS 2° Medicina ASST Spedali Civili
        • Contact:
      • Catania, Italy
        • Not yet recruiting
        • Azienda Ospedaliero-Universitaria "Policlinico - V. Emanuele", Catania Anestesia e Rianimazione UO Malattie Infettive
        • Contact:
        • Contact:
      • Cremona, Italy
        • Not yet recruiting
        • ASST Cremona Unità Operativa di Chirurgia Vascolare Dipartimento di Medicina di Laboratorio e di Radiologia- Centro Emostasi e Trombosi
        • Contact:
      • Forlì, Italy
      • Mantova, Italy
        • Not yet recruiting
        • Ospedale Carlo Poma di Mantova MALATTIE INFETTIVE Padiglione 37 Str. Lago Paiolo, 10, 46100 Mantova
        • Contact:
      • Matera, Italy
        • Not yet recruiting
        • AZIENDA OSPEDALIERA Regionale S CARLO POTENZA Struttura Complessa Interaziendale "Malattie Infettive"
        • Contact:
      • Milano, Italy
        • Not yet recruiting
        • Ospedale San Raffaele Unità Funzionale dell'Unità Operativa di Malattie Infettive Osp. San Raffaele
        • Contact:
      • Torino, Italy
        • Not yet recruiting
        • Ospedale Amedeo di Savoia Torino Università di Torino Malattie Infettive
        • Contact:
        • Contact:
      • Verona, Italy
        • Recruiting
        • Azienda Ospedaliera Universitaria Integrata Verona UOC Malattie Infettive e Tropicali
        • Contact:
        • Contact:
    • Emilia Romagna
      • Bologna, Emilia Romagna, Italy, 40138
        • Recruiting
        • Policlinico S. Orsola Malpighi Dipartimento Malattie Infettive
        • Contact:
        • Contact:
      • Parma, Emilia Romagna, Italy
        • Not yet recruiting
        • Azienda Ospedaliero-Universitaria di Parma Anestesia e Rianimazione Dipartimento di Medicina e Chirurgia
        • Contact:
        • Contact:
    • Foggia
      • San Giovanni Rotondo, Foggia, Italy
        • Recruiting
        • I.R.C.C.S. "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG) UOVD Emostasi e trombosi- Poliambulatorio Giovanni Paolo II Viale Padre Pio n.7 San Giovanni Rotondo (FG)
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • For both interventional study and observational cohort, hospitalized patients are eligible to be included if the following criteria apply:

Inclusion criteria:

  • Age >=18 y
  • Microbiologically confirmed COVID-19 infection
  • Patients with moderate to severe disease according to study definitions (see below)
  • Informed consent to participate and to use data for interventional study, only to use data for observational cohort

Exclusion Criteria:

  • Participants are excluded from the interventional study if any of the following criteria apply:

    • Thrombocytopenia (platelet count < 50.000 mm3)
    • Coagulopathy: INR (International normalized ratio) >1.5, aPTT ratio >1.4
    • Impaired renal function (clearance to creatinine less than 15 ml/min)
    • Known hypersensitivity to heparin
    • History of heparin induced thrombocytopenia
    • Presence of an active bleeding or a pathology susceptible of bleeding in presence of anticoagulation (e.g. recent haemorrhagic stroke, peptic ulcer, malignant tumors at hig risk of haemorrhages, recent neurosurgery or ophthalmic surgery, vascular aneurysms, arteriovenous malformations)
    • Body weight <45 or > 150 kg
    • Concomitant anticoagulant treatment for other indications ( eg atrial fibrillation, venous thromboembolism , prosthetic heart valves).
    • Dual antiplatelet therapy
    • Pregnant or breast-feeding women

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: a phase II single-arm interventional prospective study

Patients included in the interventional study will receive subcutaneous enoxaparin in a single daily dose of:

  • 60 mg once daily in case of body weight of 45 to 60 kg
  • 80 mg per day in case of weight from 61 to 100 kg or
  • 100 mg once daily in case of bodyweight >100 kg

Enoxaparin will be started on the first day of COVID19 diagnosis and continued for 14 days.
Drug: Enoxaparin 40 Mg/0.4 mL Injectable Solution
Subcutaneous enoxaparin 40 mg once daily for 14 days.
Other Names:
  • INHIXA 4,000 UI (40 mg) / 0.4 ml
Experimental: observational cohort study
Patients included in the observational cohort will will receive standard thrombo-prophylaxis with subcutaneous enoxaparin 40 mg/die
Drug: Enoxaparin
Subcutaneous enoxaparin for 14 days: 60 mg once daily in case of body weight of 45 to 60 kg; 80 mg once daily in case of weight from 61 to 100 kg; 100 mg once daily in case of bodyweight >100 kg
Other Names:
  • INHIXA 6,000 UI (60 mg) / 0.6 ml
  • INHIXA 8,000 UI (80 mg) / 0.8 ml
  • INHIXA 10,000 UI (100 mg)/ 1 ml

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To investigate the efficacy of enoxaparin in improving the clinical outcome of hospitalized patients with moderate-severe COVID-19.
Time Frame: 30 days and 90 days from the first LMWH subcutaneous injection
Rates of hospitalized patients dead for all-cause within 30 days and 90 days from the first LMWH subcutaneous injection
30 days and 90 days from the first LMWH subcutaneous injection
To investigate the efficacy of enoxaparin in improving the clinical outcome of hospitalized patients with moderate-severe COVID-19.
Time Frame: This evaluation will be performed at 30 days and 90 days from the first LMWH subcutaneous injection
Based on the four levels scale of severity of symptoms. Any change from one level to another will be detected for all the enrolled patients, in order to evalutate the clinical efficacy of enoxaparin on the outcome of COVID 19.
This evaluation will be performed at 30 days and 90 days from the first LMWH subcutaneous injection
To investigate the efficacy of enoxaparin in improving the clinical outcome of hospitalized patients with moderate-severe COVID-19.
Time Frame: This evaluation will be performed at 14 days (the last day of treatment adminstration), at 30 days and 90 days from the first LMWH subcutaneous injection
Evolution of the clinical severity during treatment, based on the number and rate of patients admitted to ICU and the length of their ICU stay
This evaluation will be performed at 14 days (the last day of treatment adminstration), at 30 days and 90 days from the first LMWH subcutaneous injection
To investigate the efficacy of enoxaparin in improving the clinical outcome of hospitalized patients with moderate-severe COVID-19.
Time Frame: This evaluation will be performed at 90 days from admission
Difference between groups in number of days of hospitalization from admission to discharge
This evaluation will be performed at 90 days from admission

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To analyse the safety of enoxaparin in hospitalized patients with moderatesevere COVID-19.
Time Frame: 45 days

Rate of adverse events (AEs) during treatment, at the end of treatment (EOT) and at 30 days after EOT.

• Severity of AEs classified according to common terminology criteria for adverse events (CTCAE). The worst degree ever suffered will be considered.
45 days
To describe the rates and the types of thromboembolic events among hospitalized patients with confirmed diagnosis of COVID-19.
Time Frame: 90 days
Occurrence of thromboembolic event at 90 days after COVID-19 diagnosis. Description of the type, distribution and severity of thromboembolic events.
90 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Investigators

  • Principal Investigator: Pierluigi Viale, MD, Infectious Diseases Unit, Dep. Med. and Surg. Science University of Bologna

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 22, 2020

Primary Completion (Anticipated)

October 30, 2020

Study Completion (Anticipated)

October 30, 2020

Study Registration Dates

First Submitted

May 29, 2020

First Submitted That Met QC Criteria

June 10, 2020

First Posted (Actual)

June 11, 2020

Study Record Updates

Last Update Posted (Actual)

June 17, 2020

Last Update Submitted That Met QC Criteria

June 15, 2020

Last Verified

June 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2020-001308-40

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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