First Administration to Man Of Org 25435 a New Intravenous Anesthetic

Anaesthesia Clinical Trial

Official title:

First Administration to Man Of Org 25435 a New Intravenous Anesthetic

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01062867
• Other study ID #: CT 12.4.104
• Status: Completed
• Phase: Phase 1
• First received: February 2, 2010
• Last updated: February 3, 2010
• Start date: January 2000
• Est. completion date: March 2000

Study information

• Verified date: January 2010
• Source: University of Plymouth
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Research Ethics Committee
• Study type: Interventional

Clinical Trial Summary

Title: First administration to man of Org 25435, a new intravenous anaesthetic.

Protocol: 12.4.104

Clinical Phase: Phase I

Study Site:

Phase I Clinical Trials Unit Ltd Old Convent of Notre Dame 119 Looseleigh Lane Plymouth PL6 5HH United Kingdom

Objectives: To assess the safety, tolerability, preliminary pharmacokinetics and efficacy of Org 25435 as an intravenous anaesthetic.

Study Design: Sequential study of an intravenous anaesthetic in young healthy males, at up to eight dose levels.

Study Drug: Org 25435, a water soluble intravenous anaesthetic.

Subjects: Up to 47 healthy male volunteers, aged 18-40 years.

Evaluations: Tolerability, adverse events, EEG effects, cardiovascular effects, electrocardiogram (ECG), excitatory phenomena, respiratory effects, laboratory safety blood analyses, pharmacodynamic and pharmacokinetic measurements.

Description:

Synopsis Trial Number 12.4.104 Trial Title First administration to man of Org 25435 a new intravenous anesthetic Trial Center Phase 1 Clinical Trials Unit Limited, 119 Looseleigh Lane, Derriford, Plymouth PL6 5HH Publication Studied Period The first subject was screened on 04/01/2000 and the final subject completed the follow up on 24/03/2000.

Phase of Development Phase I (First into Man) Objectives To assess the safety, tolerability and efficacy of Org 25435 as an intravenous anesthetic and to obtain preliminary pharmacodynamic and pharmacokinetic details of Org 25435.

Methodology Sequential rising dose study of an intravenous anesthetic in young healthy males, at up to eight dose levels.

Number of Subjects 19 healthy male volunteers were included into the dose escalation part of the study and an additional 7 volunteers participated in the Target Controlled Infusion (TCI) part of the study.

Diagnosis and Main Criteria for Inclusion Inclusion criteria:

Good physical and mental health: absence of a clinically relevant medical history; Clinically acceptable hematology and clinical chemistry results; Hemoglobin > 13.5 g/dl; Normal ECG; Diastolic blood pressure 60 to 90 mmHg inclusive; Normal cardiac morphology demonstrated by echocardiography; Satisfactory cardiovascular response to exercise, measured by the Bruce Protocol, subjects must have completed Bruce stage 5; Aged 18 to 35 years inclusive; Body mass index (BMI) 19 to 27 inclusive, weight 65 to 100 kg inclusive; Negative hepatitis screen; Non-smoker for at least 6 months; Previous experience of general anesthesia with no problems reported; Willingness to give written informed consent; Ability to communicate well with the Investigators.

Investigational Product Dose Mode of Administration Batch Number 1 vial 200mg Org 25435 / 10ml solvent for reconstitution Intended doses: 0.25, 0.5, 1.0, 2.0, 3.0, 4.0, 5.0 and 6.0 mg/kg Intravenous 9J521 Duration of Treatment

Dose Escalation phase:

Each study treatment consisted of an intravenous infusion of Org 25435, given by Infusion pump over exactly 1 minute.

Target Controlled Infusion phase:

Each study treatment consisted of an intravenous infusion of Org25435 given by a computer-controlled infusion over 30 minutes.

Criteria for Evaluation Tolerability, adverse events, EEG effects, cardiovascular effects, electrocardiogram (ECG), excitatory phenomena, respiratory effects, laboratory safety blood analyses, pharmacodynamic and pharmacokinetic measurements. Efficacy Induction phenomena; time of cessation of speech, eye closure, loss of eyelash reflex, eyes open on command, limb movement on command and syringe drop. Other Induction phenomena; pain on injection, sign of histamine release, excitatory phenomena, respiratory depression, apnea. Recovery phenomena; nausea / vomiting, delirium, shivering, disturbed psychomotor function, eye opening on command, spontaneous respiration, adequate respiration, move limbs on command, increased saliva production.

Statistical Methods Formal statistical methods are not appropriate in this small pilot investigative study where group sizes comprise 5 or less subjects. All data collected is presented and summarized according to investigation type (Dose Escalation or TCI).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 26
• Est. completion date: March 2000
• Est. primary completion date: March 2000
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 35 Years

Eligibility

Inclusion Criteria:

• Good physical and mental health:

• Absence of a clinically relevant medical history

• Clinically acceptable hematology and clinical chemistry results

• Hemoglobin > 13.5 g/dl

• Normal ECG

• Diastolic blood pressure 60 to 90 mmHg inclusive

• Normal cardiac morphology demonstrated by echocardiography

• Satisfactory cardiovascular response to exercise, measured by the Bruce Protocol, subjects must have completed Bruce stage 5

• Aged 18 to 35 years inclusive

• Body mass index (BMI) 19 to 27 inclusive, weight 65 to 100 kg inclusive

• Negative hepatitis screen

• Non-smoker for at least 6 months

• Previous experience of general anesthesia with no problems reported -

• Willingness to give written informed consent

• Ability to communicate well with the Investigators.

Exclusion Criteria:

• Females

• History or evidence of clinically significant cardiovascular, respiratory, endocrine, renal, hepatic, neurological or psychiatric disease.

• History of or familial presence of malignant hyperthermia.

• Presence of any condition likely to affect the normal kinetics of the study drug.

• Requirement for prescribed medication.

• Use of concomitant medication in the 5 days prior to dosing.

• General anaesthesia within the previous 3 months.

• History of clinically significant allergy or hypersensitivity to any drug.

• History of clinically significant head injury.

• History of febrile convulsion.

• Known history of human immunodeficiency virus (HIV) infection.

• Use of investigational drug within previous three months.

• Previous administration of an investigational intravenous anaesthetic drug.

• Previous administration of Org 25435 within this study.

• History of alcohol / drug abuse.

• Average consumption of more than 20 units of alcohol a week.

• Subjects who smoke or who have smoked within the past 6 months.

• Inability to communicate with the Investigators for any reason.

• Donation of blood within one month of the study, or the intention to donate blood within one month following the study.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Anaesthesia

Intervention

Drug:
• ORG25435
Intended doses: 0.25, 0.5, 1.0, 2.0, 3.0, 4.0, 5.0 and 6.0 mg/kg by intravenous infusion over 1 min Up to 25mg/kg by infusion over 30min

Locations

Country	Name	City	State
United Kingdom	Phase 1 Clinical Trials	Plymouth	Devon
United Kingdom	Phase 1 Clinical Trials Ltd	Plymouth

Sponsors (3)

Lead Sponsor	Collaborator
University of Plymouth	Organon Teknika, Veeda Clinical Research

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	induction of anaesthesia (loss of consciousness)		At time of drug administration. Recorded in minutes and seconds from the commencement of infusion.	No
Secondary	recovery from anaesthesia (obey verbal commands)		At time of drug administration. Recorded as min and sec from end of infusion	No