Sativex® and Gentamicin for Optimized Pharmagological Treatment in Older Patients (CanPan) (CanPan)

A Pharmacological Trial With Sativex® and Gentamicin for Optimized Phamacological Treatment of Older Patients With Focus on Appetite Stimulation and Renal Risk Drugs

Malnutrition and inappropriate prescribing of renally excreted drugs are common among older persons and are associated with severe consequences such as complicated courses of treatment, mortality, and reduced quality of life. The overall purpose of CanPan is to optimize treatment of older persons with malnutrition with a focus on appetite stimulation and optimized prescribing of renal risk drugs.

The CanPan trial consists of two sub-studies. Substudy 1 will provide knowledge on appetite and appetite stimulation and together, sub study 1 and 2 will offer unique knowledge on how body composition, renal function and biomarkers of organ function influence pharmacokinetics for a highly lipophilic (Sativex®) and hydrophilic (Hexamycin®) drug in older medical patients with malnutrition.

Study Overview

• Status: Recruiting
• Conditions: Anorexia; Malnutrition; Aging; Pharmacokinetics; Cannabis; Renal Function; Emergency Service, Hospital
• Intervention / Treatment: Drug: Sativex

Detailed Description

The CanPan trial consists of sub study 1 and sub study 2. Subjects who meet all the inclusion criteria and none of the exclusion criteria are invited to participate in both sub studies. Sub study 1 consist of trial days 1 and 2 and sub study 2 consists of trial day 3.

Sub study 1:

Sub study 1 is a double-blinded, randomized, placebo-controlled, multidose, crossover trial that evaluates the appetite stimulating effect as well as the pharmacokinetics of Sativex®. The primary purpose of sub study 1 is to 1) uncover whether Sativex® has appetite stimulating properties defined as increased energy intake compared to placebo, 2) to develop a pharmacokinetic-pharmacodynamic model, and gain knowledge about the effect of Sativex® on other markers of appetite, the intraocular pressure of the eye and safety parameters.

In sub study 1, subjects receive both Sativex® and placebo. Both Sativex® and placebo are administered as an oromucosal spray. Sativex consists of 2.7 mg tetrahydrocannabinol (THC) and 2.5 mg cannabidiol (CBD) per dose of spray (Cannabis sativa L. extract, cannabis leaf and flower). Subjects receive three dose of spray two times during a trial day. Trial day 1 is planned <14 days after inclusion and there is a 2-week break between trial days 1 and 2 due to a wash-out period. Follow-up visits/phonecalls are made on days 1, 2 and 7 after trial days 1 and 2.

Sub study 2:

Sub-study 2 is a single-dose pharmacokinetic study using gentamicin (Hexamycin®) as a renally excreted model drug. The purpose of sub study 2 is to compare the prediction accuracy of clearance estimates between eGFRpanel (creatinine-cystatinC-beta-2_microglobulin-beta_trace_protein, eGFRcomb (creatinine-cystatinC), eGFRcreatinine (creatinine), uCrCl (24-hour urine creatinine clearance) and mGFR (measured GFR) as covariates in population based pharmacokinetic modeling of gentamicin.

On trial day 3, gentamicin is used as the model substance for a drug that is excreted > 90% renally. Gentamicin is administered as a single dose of 5 mg/kg as an intravenous injection (bolus). The marketed drug, Hexamycin® (40 mg / mL), is used for this purpose. Trial day 3 is held within 4 weeks after trial day 2. Follow-up visits are made on day 1 and 2 after trial day 3.

• Study Type: Interventional
• Enrollment (Anticipated): 17
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: Olivia Bornæs; Phone Number: +4538623184; Email: olivia.bornaes@regionh.dk
• Study Contact Backup: Name: Morten B Houlind; Phone Number: +4538623184; Email: morten.baltzer.houlind@regionh.dk

Study Locations

• Denmark
  • Hvidovre, Denmark, 2650
    • Recruiting
    • Clinical Research Centre
    • Contact: Ove Andersen, MSc, PhD; Phone Number: 004538623335; Email: ove.andersen@regionh.dk
    • Contact: Linda Andresen, MBA; Phone Number: 004538623322; Email: linda.camilla.andresen@regionh.dk

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 63 years and older (Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• ≥65 years of age
• Admitted to the acute medical department, Hvidovre Hospital
• Can cooperate cognitively and physically (patient reported)
• Low appetite/anorexia of ageing measures by SNAQ score ≤14
• BMI ≤30 (screening)
• Able to read and understand Danish
• Postmenopausal defined as missed periods for at least 12 months before the start of the trial

Exclusion Criteria:

• Regular use of medical cannabis (patient reported)
• Use of medical cannabis within 14 days at baseline (patient reported)
• Recognized or suspected psychotic illness in the subject or the subjects family (medical record and patient report)
• Severe personality disorders (journal)
• Significant psychiatric disorder in addition to mild to moderate depression (medical record)
• Allergy to the ingredients of Sativex®, placebo and Hexamycin® (patient reported)
• Terminal diagnosis (journal)
• Liver transplant (journal)
• Chronic eGFR ≤15 mL / min2 or dialysis treatment (medical record)
• High risk of nephrotoxicity due to existing drug treatment (medical assessment)
• Pacemaker (journal)
• Epilepsy (journal)
• Recurrent seizures (journal)
• Uncontrolled hypertension (journal)
• Food intolerance to the ingredients in the test meals (patient-reported)
• Vegetarian and vegan (patient-reported)
• Unwilling to avoid driving for up to 72 hours after administration of Sativex® (patient-reported)
• Unwilling to avoid alcohol 24 hours up to test days (patient-reported)
• Patients with ascites ( journal)
• Patients with significant edema on the days of the trial (journal / visual inspection)
• In active treatment of cancer or have disseminated cancer (journal)
• Known with brain - or kidney tumor (journal)
• Known with angina pectoris or intermittent claudication
• Known with stroke, AMI, or heart failure (NYHA III-IV) within the past 5 years (journal)
• In isolation
• Obs. Covid-19

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: Quadruple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Sativex first (blinded) (3 dose of spray); Trial day 1: Sativex (3 dose of spray x 2) Trial day 2: Placebo (3 dose of spray x 2) Trial day 3: Voluntary	Drug: Sativex; Sativex® is administered as an oromucosal spray and consists of 2.7 mg tetrahydrocannabinol (THC) and 2.5 mg cannabidiol (CBD) per dosis spray (Cannabis sativa L. extract, cannabis leaf and flower). The dose (3 sprays) is administered twice, at breakfast and lunch, respectively, with approximately 4 hours between each administration.; Other Names: nabiximols
Experimental: Placebo first (blinded) (3 dose of spray); Trial day 1: Placebo (3 dose of spray x 2) Trial day 2: Sativex (3 dose of spray x 2) Trial day 3: Voluntary	Drug: Sativex; Sativex® is administered as an oromucosal spray and consists of 2.7 mg tetrahydrocannabinol (THC) and 2.5 mg cannabidiol (CBD) per dosis spray (Cannabis sativa L. extract, cannabis leaf and flower). The dose (3 sprays) is administered twice, at breakfast and lunch, respectively, with approximately 4 hours between each administration.; Other Names: nabiximols

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Difference in energy intake (kJ) between Sativex® and placebo	Measured at test meal	Trial days 1 and 2.
Differences in the objective function value of the population-based pharmacokinetic model when implementing renal clearance assessed by measured GFR (mL/min), or GFR estimates based on different endogenous markers, as covariates on gentamicin clearance	The objective function value (minus two times the log-likelihood) describes the prediction accuracy (goodness-of-fit) of a population pharmacokinetic model. A drop in the objective function value of 6.63 in a model with one (1) added covariate implemented on any specific parameter compared to a base model corresponds to a significant improvement in model fit with a p-value of 0.01 in a chi-squared test. Population-based pharmacokinetic modelling is an analysis method performed on pharmacokinetic data, i.e., plasma concentrations over time. Relevant pharmacokinetic parameters are estimated simultaneously by fitting the data to the model. The model structure is found through the analysis and determines which pharmacokinetic parameters are estimated. As a minimum, the clearance and distribution volume of the central compartment are estimated	Trial day 3.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Differences in the objective function values of the population-based models of CBD and THC when implementing bodyweight, age, and body composition factors as covariates on the pharmacokinetic parameters of the model (e.g., clearance)	The objective function value (minus two times the log-likelihood) describes the prediction accuracy (goodness-of-fit) of a population pharmacokinetic model. A drop in the objective function value of 6.63 in a model with one (1) added covariate implemented on any specific parameter compared to a base model corresponds to a significant improvement in model fit with a p-value of 0.01 in a chi-squared test. Population-based pharmacokinetic-pharmacodynamic modelling is an analysis method performed on pharmacokinetic data, i.e. plasma concentrations over time, coupled to pharmacodynamic data. Relevant pharmacokinetic and -dynamic parameters are estimated simultaneously by fitting the data to the model. The model structure is found through the analysis and determines which pharmacokinetic and -dynamic parameters are estimated. As a minimum, the clearance and distribution volume of the central compartment are estimated	Trial days 1 and 2.
Difference in subjective appetite between Sativex® and placebo	Using combined subjective appetite scores measured using 100-mm Visual Analogue Scales (VAS), with 0.0 as the minimum value and 10.0 as the maximum value. The following will be used to calculate a combined appetite score: [desire to eat + hunger + prospective food consumption + (10.0 - fullness) + (10.0 - satiety)], with higher scores indicating better appetite.	Trial days 1 and 2.
Differences in the appetite hormones, total ghrelin and glucagon like peptide 1 (GLP-1) between Sativex® and placebo	The appetite hormones (total ghrelin, GLP-1) is measured from blood samples	Trial days 1 and 2.
Change in the intraocular pressure of the eye between Sativex® and placebo	Measured by Icare ic100 tanometer	Trial days 1 and 2.
Safety parameter (CNS effects) for Sativex®	Measured using 100-mm Visual Analogue Scales (VAS), with 0.0 as the minimum value and 10.0 as the maximum value. Higher scores indicate a larger effect.	Trial days 1 and 2.
Safety parameter (cognition) for Sativex®	Measured using Hopkins Verbal Learning Test-Revised for a total score of the following sub-tests: 'Total recall', 'Delayed recall', 'Retention' and 'Recognition'. Higher scores indicate better performance.	Trial days 1 and 2.
Safety parameter (balance disorders) for Sativex®	Bergs Balance Test is used to measure balance disorders. Balance disorders are defined as a summerated score of ≤45.	Trial days 1 and 2.
Safety parameter (blood pressure) for Sativex®	Blood pressure is measured in millimeter of mercury (mmHg) using automatic standardized equipment.	Trial days 1 and 2.
Safety parameter (heart rate) for Sativex®	Heart rate is measured in beats per minute (bpm) using automatic standardized equipment.	Trial days 1 and 2.
Correlation coefficient between clearance of gentamicin and clearance determined as mGFR or eGFR	Pharmacokinetic modeling	Trial day 3.
Change in plasma creatinine µmol/L between baseline and 22 hours after administration of gentamicin	Changes in kidney biomarkeres before and after administration of gentamicin	Trial day 3
Change in plasma cystatin C mg/L between baseline and 22 hours after administration of gentamicin	Changes in kidney biomarkers before and after administration of gentamicin	Trial day 3
Change in plasma NGAL ng/mL between baseline and 22 hours after administration of gentamicin	Changes in kidney biomarkers before and after administration of gentamicin	Trial day 3
Change in plasma KIM-1 pg/mL between baseline and 22 hours after administration of gentamicin	Changes in kidney biomarkers before and after administration of gentamicin	Trial day 3

Collaborators and Investigators

• Sponsor: Ove Andersen
• Collaborators: University of Copenhagen; Glostrup University Hospital, Copenhagen; University Hospital Bispebjerg and Frederiksberg; Region Hovedstadens Apotek; North Denmark Regional Hospital
• Investigators: Study Chair: Ove Andersen, Hvidovre University Hospital; Study Chair: Rikke L Nielsen, Hvidovre University Hospital

Study record dates

Study Major Dates

• Study Start (Actual): March 24, 2022
• Primary Completion (Anticipated): August 1, 2023
• Study Completion (Anticipated): September 1, 2023

Study Registration Dates

• First Submitted: April 13, 2022
• First Submitted That Met QC Criteria: August 15, 2022
• First Posted (Actual): August 16, 2022

Study Record Updates

• Last Update Posted (Actual): September 21, 2022
• Last Update Submitted That Met QC Criteria: September 16, 2022
• Last Verified: September 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Disease Attributes; Signs and Symptoms, Digestive; Nutrition Disorders; Anorexia; Emergencies; Malnutrition; Physiological Effects of Drugs; Peripheral Nervous System Agents; Analgesics; Sensory System Agents; Nabiximols
• Other Study ID Numbers: H-21044231

Drug and device information, study documents

• 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