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Completed

NCT Number: NCT04570384

Intravenous L-Citrulline Influence on the Need for Invasive Mechanical Ventilation for Acute Hypoxemic Respiratory Failure in Patients With COVID-19

Prospective, Randomized, Double-Blind, Placebo-Controlled Phase II Trial of Intravenous L-Citrulline (Turnobi) to Delay and Potentially Prevent the Need for Invasive Mechanical Ventilation for Acute Hypoxemic Respiratory Failure in Patients with COVID-19 (SARS-CoV2) Illness. To evaluate safety and efficacy of a bolus loading dose and continuous intravenous infusion of L-Citrulline compared to placebo in patients hospitalized with COVID-19 infection (SARS-CoV-2).

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of Arkansas for Medical Sciences

Little Rock, Arkansas, 72205, United States

About this study

Intravenous L-citrulline (Turnobi) administration will safely restore the homeostasis of nitric oxide synthase by increasing both plasma citrulline and arginine levels. Investigators also reason that restoration of citrulline/arginine balance through citrulline administration will safely re-establish homeostasis of NOS, lower oxidative stress, and reduce inflammation, thereby delaying and potentially preventing the need for invasive mechanical ventilation in participants hospitalized with COVID-19 infection (SARS-CoV-2). The body lives in a delicate balance of homeostasis. The urea/NO cycle plays a critical role in maintaining redox homeostasis and as such, also plays a role in regulating inflammation. The biochemical relationships are complex and depend on inter-organ transfer, membrane transport, and intracellular compartmentation. However, data above demonstrate that citrulline, arginine, and NO are critical in maintaining this homeostasis through their regulation of NOS. Inflammation, especially from infection, results in decreased activity of CPS1 and increased activity of arginase, which decreases levels of both citrulline and arginine. These decreased levels result in dysregulated and uncoupled NOS, which drives both overexuberant NO production and formation of ROS. Both the NO production and ROS further exacerbate the inflammatory cascade, resulting in other organ dysfunctions, including acute lung injury. Both inflammation and oxidative stress have been shown to be driving forces for the development of ALI and regulated NOS function is vital to reducing both. Both plasma citrulline and arginine are deficient in sepsis and levels are inversely associated with development of ALI. Furthermore, citrulline replacement safely increases plasma levels of both citrulline and arginine in healthy volunteers, BMT patients, adults with sepsis, children with sickle cell disease, and children after congenital heart surgery. It seems highly likely that citrulline therapy in the setting of COVID-19 (SARS-CoV2) induced acute hypoxemic respiratory illness will safely increase citrulline and arginine levels and help re-establish NOS homeostasis, resulting in NO production in compartments that are more homeostatically appropriate so as to reduce pulmonary vascular resistance and enhance coupling of NOS to minimize superoxide production thus reducing free radical mediated ALI.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-65 years.
  • Clinical evidence of COVID-19 (SARS-CoV2) infection, defined as a positive COVID-19 laboratory test plus evidence of an acute hypoxemic respiratory illness requiring oxygen.
  • Admitted and transferred to floor without intubation.

Exclusion criteria

  • No consent/inability to obtain consent
  • Patient, surrogate, or physician not committed to full support
  • Malignant or other irreversible condition and estimated 28-day mortality ≥ 50%
  • Moribund patient not expected to survive 48 hours (as defined by primary medical team) from start of study infusion
  • End-stage Liver Disease as defined by Child-Pugh Score > 9
  • Currently enrolled in, or participated in another study of an investigational compound within the last 30 days
  • Pregnant female, or female who is breast feeding
  • Allergy to L-citrulline or arginine or any citrulline- or arginine-containing product
  • Patient not otherwise suitable for the study in the opinion of any of the investigators
  • Requirement for intubation and invasive mechanical ventilation before study enrollment

Treatment and study plan

L-citrulline

Drug

L-Citrulline (Turnobi) for Injection. Patients will receive an initial bolus of 20 mg/kg (maximum 1500 mg), followed by study infusion of 9 mg/kg per hour (maximum 700mg) for up to 10 days.

Other names: L-CIT, CIT

Placebo

Drug

Patients randomized to placebo will receive equal volume bolus and study infusion of 5% dextrose water for a maximum of 10 days.

Primary outcomes

  1. Time to Non-invasive/Invasive Mechanical Ventilation

    Time frame: From the start of infusion to Day 60 Follow-up

    Time in hours from the initiation of the treatment until mechanical ventilation is required, whether non-invasive (e.g., high flow nasal cannula, bilevel positive airway pressure, oxygen therapy) or invasive (i.e., requiring intubation).

  2. Time to Non-invasive Mechanical Ventilation

    Time frame: From the start of infusion to Day 60 Follow-up

    Time in hours from the initiation of the treatment until non-invasive mechanical ventilation is required (e.g., high flow nasal cannula, bilevel positive airway pressure, oxygen therapy) .

  3. Time to Invasive Mechanical Ventilation

    Time frame: From the start of infusion to Day 60 Follow-up

    Time in hours from the initiation of the treatment until intubation for invasive mechanical ventilation is required.

  4. Systolic Blood Pressure

    Time frame: Day 1

    Systolic blood pressure measured in mmHg

  5. Diastolic Blood Pressure

    Time frame: Day 1

    Diastolic blood pressure measured in mmHg

  6. Mean Arterial Pressure

    Time frame: Day 1

    Mean arterial pressure measured in mmHg

Secondary outcomes

  1. Blood Levels of Arginine

    Time frame: Plasma levels of arginine at 0, 2 and 12 hours, and 2, 4, 6, 8, 10 days after initiation of treatment

    Plasma levels of arginine

  2. Blood Levels of Citrulline

    Time frame: Plasma levels of citrulline at 0, 2 and 12 hours, and 2, 4, 6, 8, 10 days after initiation of treatment

    Plasma levels of citrulline

  3. Evaluate the Effect of Intravenous L-Citrulline Compared to Placebo as Measured by the Total Length of All Mechanical Ventilation

    Time frame: Day 1 through Day 60 Follow Up

    Total length of time of any mechanical ventilation

  4. Evaluate the Effect of IV L-Citrulline to Placebo for Hospital All Cause Mortality

    Time frame: Day 1 through day 12

    To evaluate the effect of intravenous L-Citrulline compared to placebo on Hospital all-cause mortality

  5. Percentage of Patients Admitted to Intensive Care

    Time frame: Day 1 through Day 12 (DC)

  6. Duration of Intensive Care Unit (ICU) Stay

    Time frame: From admission to ICU until discharge or death

    Length of ICU stay (days)

  7. Duration of Hospitalisation

    Time frame: From admission to hospital until discharge or death

    Length of hospital stay (days)

  8. Number of Patients Requiring Intubation

    Time frame: From the start of infusion to Day 60 Follow-up

    Percentage of patients requiring any mechanical ventilation, invasive mechanical ventilation and non-invasive mechanical ventilation.

  9. Overall Duration of Mechanical Ventilation

    Time frame: From the start of infusion to Day 60 Follow-up

    Total time on any mechanical ventilation, invasive mechanical ventilation, non-invasive mechanical ventilation and nasal cannula

Sponsors and collaborators

Lead sponsor

Asklepion Pharmaceuticals, LLC

Industry

Registry information

Official study title

Prospective, Randomized, Double-Blind, Placebo-Controlled Phase II Trial of Intravenous L-Citrulline (Turnobi) to Delay and Potentially Prevent the Need for Invasive Mechanical Ventilation for Acute Hypoxemic Respiratory Failure in Patients With COVID-19 (SARS-CoV-2) Illness

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Sep 30, 2020
Registry last updated
Feb 22, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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