A Study in Healthy Male Volunteers to Investigate the Safety and Tolerability of a Single Dose of Neosaxitoxin Alone and in Combination With Bupivacaine (With and Without Epinephrine) for Brachial Plexus Blockade

Anesthesia Clinical Trial

Official title:

An Exploratory Phase I Randomized, Single-site, Double-blind, Active-controlled, Parallel-group, Single-administration, Dose-escalation Trial to Investigate the Safety and Tolerability of Neosaxitoxin Alone and in Combination With Bupivacaine (With and Without Epinephrine), in Perineural Administrations for Brachial Plexus Blockade in Healthy Subjects

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03399435
• Other study ID #: HP7020-02
• Secondary ID: 2016-003958-33U1
• Status: Terminated
• Phase: Phase 1
• Start date: January 30, 2018
• Est. completion date: September 21, 2018

Study information

• Verified date: October 2018
• Source: Grünenthal GmbH
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Neosaxitoxin is a new compound that is in clinical development as local anesthetic for surgical anesthesia and postoperative analgesia.

The primary objective of this study is to evaluate the systemic and local safety and tolerability of ascending doses of neosaxitoxin alone and in combination with fixed doses of bupivacaine (with and without epinephrine), following brachial plexus blockade in healthy male subjects.

Secondary objectives:

• Evaluate the pharmacodynamics (PD) of ascending doses of neosaxitoxin, alone and in combination with fixed doses of bupivacaine (with and without epinephrine), following brachial plexus blockade.

• Characterize the pharmacokinetics (PK) of neosaxitoxin and bupivacaine after brachial plexus blockade with neosaxitoxin alone or different drug combinations: neosaxitoxin and epinephrine, neosaxitoxin and bupivacaine, or neosaxitoxin and bupivacaine and epinephrine.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 242
• Est. completion date: September 21, 2018
• Est. primary completion date: September 21, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Subject has given written informed consent to participate.

• Male subject, aged 18 years to 55 years, inclusive.

• Body mass index between 20.0 kg/m2 and 30.0 kg/m2 inclusive, with a minimal body weight of 60.0 kg.

• Subject must be in good health as determined by the prior/concomitant diseases, physical and laboratory examinations.

• Subject must be willing not to donate sperm and to use barrier contraception (condom) during sexual intercourse with women from the administration of IMP until Day 90 since IMP administration. The subject must be willing to ensure that the female sexual partner of childbearing potential uses at least 1 additional method of contraception with a low failure rate defined as <1% per year (e.g., oral contraceptives) during this time frame. A single barrier method alone is not acceptable.

Exclusion Criteria:

At enrollment:

• Resting pulse rate <50 beats or >90 beats per minute.

• Resting systolic blood pressure <90 mmHg or >140 mmHg. Resting diastolic blood pressure >90 mmHg.

• Prolongation of QTcF at enrollment, i.e., QTcF >450 ms, or presence of any other of risk factors for torsade de pointes or other disturbances of cardiac de- and repolarization.

• Any out-of-reference range value for the following safety laboratory parameters: GGT, serum creatinine, PT, and INR.

• Any exclusion range met for urinalysis and the following safety laboratory parameters:

ALT, AST, ALP, total bilirubin, glucose, LDH, potassium, total protein, sodium, calcium, CK, hemoglobin, hematocrit, white blood cell count, and platelets.

• Any out-of-reference range value for any other safety laboratory parameter that is judged as clinically relevant by the investigator.

• Positive or missing virus serology test for HIV Type 1 or Type 2 antibodies and antigen, hepatitis B surface antigen, hepatitis B core antibodies, or hepatitis C virus antibodies.

• Subject received IMP in another clinical trial within 1 month before the Enrollment Visit. Depending on the nature of the previous IMP, a longer washout may be needed.

• Diseases or conditions known to interfere with the distribution, metabolism, or excretion of drugs.

• History of orthostatic hypotension.

• History of, or at risk of seizures.

• Significant cardiovascular, respiratory, neuromuscular diseases, or other systemic illness.

• Subject with an oxygen saturation of less than 95%, as measured by pulse oximetry, or subject with known or suspected respiratory difficulty or any condition that may compromise a subject's breathing or ability to maintain adequate oxygen saturation.

• Known vocal chord palsy.

• Any relevant symptom of neurological dysfunction of the motor and sensory system based on sensory and motor function testing. History or presence of symptoms of depression or anxiety disorders.

• Previous injury or surgery of the involved shoulder in the last 2 years.

• Any relevant local abnormality at the targeted area of injection.

• Any acute or chronic pain condition requiring ongoing treatment or limiting daily activities.

• Definite or suspected history of drug allergy, particularly to bupivacaine or other local anesthetics, epinephrine, or clinically relevant other allergies.

• Evidence or history of alcohol or drug abuse including positive or missing drugs of abuse screen.

• Regular use of any medication, including herbal remedies or over-the counter medication within 2 weeks before enrollment into this trial and anticipated use during the course of the trial.

• Habitually smoking more than 10 cigarettes, 2 cigars, or 2 pipes of tobacco per day within the last 6 months before enrollment in this trial.

• Known or suspected of not being able to comply with the requirements of the trial protocol or the instructions of the trial site staff.

• Not able to communicate meaningfully with the trial site staff.

• Employee of the investigator or trial site, with direct involvement in the proposed trial or other trials under the direction of that investigator or trial site, as well as family members of the employees or the investigator.

• Blood loss of 500 mL or more within 3 months before enrollment in this trial.

On Day -1:

• Any relevant deterioration in the health of the subject since the Enrollment Visit possibly impacting participation in the trial, including AEs, safety laboratory parameters, vital signs, body temperature, ECG, or other safety parameters at the discretion of the investigator.

• Out-of-reference blood pressure or pulse rate if technical failure can be excluded and result is confirmed by at least 1 additional measurement: Systolic blood pressure <90 mmHg or >140 mmHg, diastolic blood pressure >90 mmHg, pulse rate <50 beats or >90 beats per minute.

• Clinically relevant QTcF interval prolongation, i.e., QTcF interval >450 ms.

• Any out-of-reference range value for the following safety laboratory parameters: GGT, serum creatinine, PT, and INR.

• Any exclusion range met for urinalysis and the following safety laboratory parameters:

ALT, AST, ALP, total bilirubin, glucose, LDH, potassium, total protein, sodium, calcium, CK, hemoglobin, hematocrit, white blood cell count, and platelets.

• Any out-of-reference range value for any other safety laboratory parameter that is judged as clinically relevant by the investigator.

• Positive or missing drugs of abuse screen.

• Intake of forbidden medication since the enrollment in this trial.

• Participation in another clinical trial since the Enrollment Visit.

• Blood loss of 100 mL or more since enrollment in this trial.

• Failure to comply with trial requirements, e.g., consumption of alcohol, etc., considered by the investigator to affect subject safety or interfere with the integrity of the trial.

• Any relevant local abnormality at the targeted area of injection.

Related Conditions & MeSH terms

• Analgesia
• Anesthesia
• Anesthesia, Local

Intervention

Combination Product:
• Neosaxitoxin combined with bupivacaine low and epinephrine (T1)
A single injection: Neosaxitoxin from 1.25 to 60 µg. Bupivacaine 40 mg. Epinephrine 100 µg.
• Bupivacaine low combined with epinephrine (C1)
A single injection: Bupivacaine 40 mg. Epinephrine dose 100 µg.
• Bupivacaine high combined with epinephrine (C2)
A single injection: Bupivacaine 100 mg. Epinephrine 100 µg.
• Neosaxitoxin combined with bupivacaine low (T2)
A single injection: Neosaxitoxin from 1.25 to 60 µg. Bupivacaine from 10 to 80 mg.

Drug:
• Bupivacaine low (C3)
A single injection: Bupivacaine from 10 to 80 mg.
• Bupivacaine high (C4)
A single injection: Bupivacaine 100 mg.
• Neosaxitoxin (T3)
A single injection: Neosaxitoxin will be between 1.25 and 60 µg.

Combination Product:
• Neosaxitoxin combined with epinephrine (T4)
A single injection: Neosaxitoxin will be between 1.25 and 60 µg. Epinephrine 100 µg.
• Neosaxitoxin combined with bupivacaine low and epinephrine
A single injection: Neosaxitoxin will be between 1.25 to 60 µg. Bupivacaine dose based on results from Part B (10 to 80 mg). Epinephrine 100 µg.
• Neosaxitoxin combined with bupivacaine low
A single injection: Neosaxitoxin will be between 1.25 to 60 µg. Bupivacaine dose based on results from Part B (10 to 80 mg).

Locations

Country	Name	City	State
Netherlands	NL001	Groningen

Sponsors (1)

Lead Sponsor	Collaborator
Grünenthal GmbH

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Occurrence of dose limiting events (DLEs) in all parts of the trial.		up to 15 days after IMP (investigational medicinal product, i.e. study drug administration)
Primary	Occurrence of other adverse events (AEs) leading to premature termination of dose escalation in Part A and Part B.		up to 15 days after IMP administration
Secondary	Cold detection threshold (CDT).		Baseline, 24 and 48 hours after IMP administration
Secondary	Warm detection threshold (WDT)		Baseline, 24 and 48 hours after IMP administration
Secondary	Mechanical detection threshold (MDT)		Baseline, 24 and 48 hours after IMP administration
Secondary	Cold pain threshold (CPT)		Baseline, 24 and 48 hours after IMP administration
Secondary	Heat pain threshold (HPT)		Baseline, 24 and 48 hours after IMP administration
Secondary	Mechanical pain threshold (MPT)		Baseline, 24 and 48 hours after IMP administration
Secondary	Muscle grip strength (ipsilateral)		Baseline, 24 and 48 hours after IMP administration
Secondary	Muscle motor function (flexion and extension elbow joint, abduction shoulder joint)		Baseline, 24 and 48 hours after IMP administration
Secondary	AUC0-t of neosaxitoxin		up to 56 hours after IMP administration
Secondary	AUC0-t of bupivacaine		up to 56 hours after IMP administration
Secondary	Cmax of neosaxitoxin		up to 56 hours after IMP administration
Secondary	Cmax of bupivacaine		up to 56 hours after IMP administration
Secondary	tmax of neosaxitoxin		up to 56 hours after IMP administration
Secondary	tmax of bupivacaine		up to 56 hours after IMP administration