A Study of LJPC‑501 in Pediatric Patients With Hypotension

Sepsis Clinical Trial

Official title:

An Open-Label, Multi-Center Study of LJPC‑501 in Pediatric Patients Who Remain Hypotensive Despite Receiving Fluid Therapy and Vasopressor Therapy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03431077
• Other study ID #: LJ501-CRH02
• Status: Completed
• Phase: Phase 2
• Start date: February 11, 2018
• Est. completion date: April 14, 2018

Study information

• Verified date: August 2018
• Source: La Jolla Pharmaceutical Company
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to evaluate the effect of LJPC-501 infusion on mean arterial pressure (MAP) or reduction in sum norepinephrine (NE) equivalent dosing, at Hour 2 after the start of LJPC-501, in pediatric patients who remain hypotensive despite receiving fluid therapy and vasopressor therapy. In addition, this study will evaluate the safety and tolerability of LJPC-501 in pediatric patients, the change in MAP over 24 hours after the start of LJPC-501, the change in serum lactate concentrations, and the change in Pediatric Logistic Organ Dysfunction (PELOD) scores.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 2
• Est. completion date: April 14, 2018
• Est. primary completion date: April 14, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years to 17 Years

Eligibility

Inclusion Criteria:

1. Pediatric patients 2-17 years of age.

2. Patients requiring a total sum NE equivalent dose of > 0.1 µg/kg/min for a minimum of 2 hours and a maximum of 48 hours prior to initiation of LJPC-501 dosing.

3. Patients must have clinical diagnosis of distributive shock in the opinion of the treating team and the Investigator.

4. Patients are required to have central venous access, which is expected to remain present for the duration of LJPC-501 treatment.

5. Patients are required to have an indwelling arterial line, which is expected to remain present for at least the first 24 hours of LJPC-501 treatment.

6. Patients must have received at least 40 mL/kg of crystalloid or colloid equivalent over the initial 24-hour resuscitation period, and are adequately volume resuscitated in the opinion of the Investigator.

7. Parent or legal guardian is willing and able to provide informed consent and assist the patient in complying with all protocol requirements.

Exclusion Criteria:

1. Patients who are < 2 years of age or = 18 years of age.

2. Patients with a standing Do Not Resuscitate order.

3. Patients diagnosed with acute occlusive coronary syndrome requiring pending intervention.

4. Patients on veno-arterial (VA) extracorporeal membrane oxygenation (ECMO).

5. Patients who have been on veno-venous (VV) ECMO for less than 6 hours.

6. Patients with a clinical suspicion of cardiogenic shock.

7. Patients who have a history of asthma or are currently experiencing bronchospasm requiring the use of inhaled bronchodilators and who are not mechanically ventilated.

8. Patients with acute mesenteric ischemia or a history of mesenteric ischemia.

9. Patients with active bleeding AND an anticipated need of multiple transfusions (within 48 hours of Screening).

10. Patients with active bleeding AND hemoglobin < 7 g/dL or any other condition that would contraindicate serial blood sampling.

11. Patients with an absolute neutrophil count (ANC) of < 500 cells/mm3.

12. Patients requiring more than 5 mg/kg daily of hydrocortisone or equivalent glucocorticoid medication as a standing dose.

13. Patients with an expected lifespan of < 12 hours or withdrawal of life support within 24 hours of Screening.

14. Patients with a known allergy to mannitol.

15. Patients who are currently participating in another investigational clinical trial.

16. Patients of childbearing potential who are known to be pregnant at the time of Screening.

Related Conditions & MeSH terms

• Catecholamine-resistant Hypotension (CRH)
• Distributive Shock
• High Output Shock
• Hypotension
• Sepsis
• Shock

Intervention

Drug:
• Angiotensin II
Angiotensin II is a peptide hormone naturally produced by the body that regulates blood pressure via vasoconstriction and sodium reabsorption. LJPC-501 (angiotensin II) is being developed for the treatment of hypotension in patients who do not respond to fluids and vasopressor therapy.

Locations

Country	Name	City	State
United States	Investigational Site	Charlotte	North Carolina
United States	Investigational Site	Cincinnati	Ohio
United States	Investigational Site	San Antonio	Texas

Sponsors (1)

Lead Sponsor	Collaborator
La Jolla Pharmaceutical Company

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Effect of LJPC-501 on mean arterial pressure (MAP)	To evaluate the effect of LJPC-501 infusion on mean arterial pressure (MAP).	2 hours
Primary	Effect of LJPC-501 on sum norepinephrine (NE) equivalent dose	To evaluate the effect of LJPC-501 in the reduction of the sum norepinephrine (NE) equivalent dosing.	2 hours
Secondary	Effect of LJPC-501 on the incidence of treatment-emergent adverse events		Day 7
Secondary	Effect of LJPC-501 on mean arterial pressure (MAP)	To evaluate the change in MAP over 24 hours after the start of LJPC-501.	24 hours
Secondary	Effect of LJPC-501 on serum lactate	To evaluate the change in serum lactate concentrations.	2 hours and 24 hours
Secondary	Effect of LJPC-501 on Pediatric Logistic Organ Dysfunction (PELOD)	To evaluate change in Pediatric Logistic Organ Dysfunction (PELOD) score from Screening to 24 hours. The PELOD score is the sum of 6 individual item scores that totals 0-71 points. A higher PELOD score represents a worse outcome.	24 hours
Secondary	Effect of LJPC-501 on clinical chemistry laboratory parameters	Safety data for clinical chemistry parameters including ALT, AST, ALP, total bilirubin, direct bilirubin, creatinine, BUN, phosphorus, glucose, albumin, calcium, bicarbonate, chloride, sodium, potassium, magnesium, PT, PTT, and INR. In addition, serum pregnancy test will be assessed at screening to confirm eligibility.	24 hours
Secondary	Effect of LJPC-501 on hematology laboratory parameters	Safety data for laboratory hematology parameters including hemoglobin, hematocrit, platelets, and WBC.	24 hours
Secondary	Effect of LJPC-501 on blood pressure	Change in blood pressure (mmHg).	Day 7
Secondary	Effect of LJPC-501 on heart rate	Change in heart rate (bpm).	Day 7
Secondary	Effect of LJPC-501 on body temperature	Change in body temperature (Celsius).	Hour 24
Secondary	Effect of LJPC-501 on general health	Change in physical examination (by body system).	Day 7
Secondary	Effect of LJPC-501 on electrical activity of the heart	Change in the electrical activity of the heart over a period of time using electrodes placed on the skin and recorded by electrocardiogram (ECG).	Hour 24
Secondary	Effect of LJPC-501 on urine output	Change in urine output (ml).	Day 7