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The Treatment of Adrenal Crisis With Inhaled Prednisolone (TRACER)

Primary Purpose

Adrenal Insufficiency

Status
Recruiting
Phase
Early Phase 1
Locations
Netherlands
Study Type
Interventional
Intervention
Prednisolone
Sponsored by
University Medical Center Groningen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adrenal Insufficiency

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Age: 18 - 75 years Woman who use reliable contraceptives or with a negative pregnancy test Equal sex distribution Exclusion Criteria: Heart failure Known liver or kidney disease Dependency on glucocorticoids Adrenogenital syndrome Infectious disease Uncontrolled hypertension defined as a blood pressure > 180/110 mmHg Pregnancy or breastfeeding Use of medication that interferes with cytochrome P450 (e.g. carbamazepine)

Sites / Locations

  • UMCGRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Low dose, wash out, high dose

Arm Description

Outcomes

Primary Outcome Measures

Tmax
The time from nebulization to peak concentration prednisolone (Tmax (min))
AUC
The area under the curve (AUC (h*nmol/L))

Secondary Outcome Measures

Cmax
Peak concentration (Cmax (nmol/L))
T1/2
Half life (T1/2 (h))
CL
Total Body Clearance (CL (L/h))
Vd
Volume of distribution (Vd (L))

Full Information

First Posted
August 25, 2022
Last Updated
November 24, 2022
Sponsor
University Medical Center Groningen
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1. Study Identification

Unique Protocol Identification Number
NCT05639127
Brief Title
The Treatment of Adrenal Crisis With Inhaled Prednisolone
Acronym
TRACER
Official Title
Novel Treatment of Adrenal Crisis: an Early Clinical Trial With Nebulized Prednisolone
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 3, 2022 (Actual)
Primary Completion Date
November 30, 2022 (Anticipated)
Study Completion Date
March 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Medical Center Groningen

4. Oversight

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
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Rationale: An adrenal crisis is an acute life-threatening event which may occur in patients with adrenal insufficiency. The initial emergency treatment consists of an intramuscular injection with 100 mg hydrocortisone administered by the patient or a bystander. The injection should be administered immediately. Although it is considered life-saving, it is not very patient-friendly, because of the several steps required for reconstitution, the intramuscular injection, the frequent presence of needle phobia, and pain at the injection site. Inhalation of predniso(lo)ne could be a more patient-friendly alternative. Objective: This study investigates the pharmacokinetics of nebulized prednisolone in two different dosages. Study design: Single-center, open-label study Study population: Healthy participants aged 18-75 years. Intervention (if applicable): Healthy volunteers receive a lower dose of nebulized prednisolone (46.75 mg).After a wash-out period of at least one week, each volunteer receives a higher dose of nebulized prednisolone (93.5 mg). Main study parameters/endpoints: To establish the time from nebulizing to maximum prednisolone concentration in serum and the area under the curve of prednisolone. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Participants are exposed to a single supraphysiological dose of glucocorticoids on two separate occasions. The risk of SAE is very limited. There is a small risk of an AE during blood sampling. If it is demonstrated that therapeutic plasma concentrations of prednisolone can be reached by nebulizing prednisolone, we intend to use the pharmacokinetic data to design and perform a clinical study with a dry-powder micronized prednisone inhalation. This would represent a novel and promising alternative treatment for an adrenal crisis. Patients with adrenal insufficiency could then be offered a much more patient-friendly and reliable alternative for intramuscular hydrocortisone injection.
Detailed Description
The prevalence of adrenal insufficiency is approximately 30-50 individuals per 100.0001. Patients with adrenal insufficiency rely on glucocorticoid substitution therapy (hydrocortisone or cortisone acetate). In case of an acute stressful situation, e.g. illness, trauma, or psychological stress, the standard substitution dose falls short and patients need to increase their glucocorticoid dose to prevent a cortisol deficiency which could ultimately lead to an adrenal crisis. The incidence of an adrenal crisis is about 5-10 cases per year 100 patient-years and is characterized by hypotension, nausea, hyponatremia, hyperkalemia, hypoglycemia, and a circulatory shock with the risk of a fatal outcome2,3. Acute glucocorticoid administration in case of an adrenal crisis is a life-saving procedure. Currently, patients have to inject themselves with an intramuscular injection of hydrocortisone sodium succinate, corresponding with 100 mg hydrocortisone. This mode of self-treatment has several disadvantages. Hydrocortisone sodium succinate is an unstable product in solution, it is therefore available as Solu-cortef Act-O-Vial in two-chamber vials containing hydrocortisone powder and diluent solution separately. The patient should first prepare the solution and then self-administer the hydrocortisone solution by an intramuscular injection. This is a multistep procedure (Supplement 1). If the injected dose is insufficient, a second injection might be necessary. In addition, patients with an (imminent) adrenal crisis often experience confusion, drowsiness, dizziness, and nausea with vomiting. As a result, patients may be incapacitated to self-administer intramuscular hydrocortisone. Moreover, needle phobia might hamper self-injection of hydrocortisone. Furthermore, patients are advised to always carry the Solu-Cortef® Act-O-vial, syringe, and needles with them. This is, however, often not very practical and many patients do not follow up on this recommendation. These disadvantages of self-injection of hydrocortisone create a barrier for optimal emergency treatment. It is therefore logical that this method of drug administration is often not sufficiently used and easily leads to errors. Notably, we recently published data about adrenal crises in our own UMCG population and concluded that less than half of the patients who experienced an adrenal crisis used their emergency medication4. A small inhalation device containing micronized prednisone seems a promising alternative for the replacement of the hydrocortisone injection. It is known that several drugs have a similar time from administration to effect after inhalation as after injection. Examples are adrenaline, levodopa, morphine, and insulin5. Based on its physicochemical properties, prednisone is expected to be as rapidly distributed into the bloodstream after inhalation compared to an intramuscular injection. In addition, previous application of inhaled prednisone for patients with asthma and COPD has demonstrated that the inhalation of prednisone is safe6. A major advantage to prednisone inhalation compared to the Solu-Cortef® injection is that difficult reconstitution procedures are no longer necessary. In addition, the prednisone powder within the inhalator is very stable and easy to carry along as it fits inside a small pocket. Moreover, in contrast to intramuscular self-injection, inhalation treatment is pain-free and is expected to be acceptable for the majority of patients The patient's resistance against inhalation is much less than against the injection. As the first step in the development of this prednisone inhaler we will investigate if therapeutic plasma concentrations of prednisolone can be reached by nebulizing prednisolone. In this study, we administer nebulized prednisolone in two different dosages to healthy volunteers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adrenal Insufficiency

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Model Description
Open label single group
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Low dose, wash out, high dose
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Prednisolone
Intervention Description
Nebulization of prednisolone
Primary Outcome Measure Information:
Title
Tmax
Description
The time from nebulization to peak concentration prednisolone (Tmax (min))
Time Frame
4 hours
Title
AUC
Description
The area under the curve (AUC (h*nmol/L))
Time Frame
4 hours
Secondary Outcome Measure Information:
Title
Cmax
Description
Peak concentration (Cmax (nmol/L))
Time Frame
4 hours
Title
T1/2
Description
Half life (T1/2 (h))
Time Frame
4 hours
Title
CL
Description
Total Body Clearance (CL (L/h))
Time Frame
4 hours
Title
Vd
Description
Volume of distribution (Vd (L))
Time Frame
4 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age: 18 - 75 years Woman who use reliable contraceptives or with a negative pregnancy test Equal sex distribution Exclusion Criteria: Heart failure Known liver or kidney disease Dependency on glucocorticoids Adrenogenital syndrome Infectious disease Uncontrolled hypertension defined as a blood pressure > 180/110 mmHg Pregnancy or breastfeeding Use of medication that interferes with cytochrome P450 (e.g. carbamazepine)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Annet Vulto, MD
Phone
+31503617293
Email
a.vulto@umcg.nl
Facility Information:
Facility Name
UMCG
City
Groningen
ZIP/Postal Code
9713 GZ
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
André P van Beek, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Upon reasonable request
IPD Sharing Time Frame
After completion study
IPD Sharing Access Criteria
Upon reasonable request

Learn more about this trial

The Treatment of Adrenal Crisis With Inhaled Prednisolone

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