Clinical Drug Experience Knowledgebase

Criteria

Inclusion Criteria:

Males or females between 18 and 65 years of age scheduled for low- or moderate-risk surgical procedure requiring tracheal intubation

Female patients must not be of child-bearing potential. Females must meet one of the following criteria:

Be postmenopausal;
Have undergone prior tubal ligation or hysterectomy; or
Be scheduled for hysterectomy as the surgical procedure for this study.
American Society of Anesthesiologists (ASA) Physical Status Classification 1 or 2
Weight within 30% of ideal body weight
Able to read and to comprehend information about the study design and procedure; willingness to participate in this study as evidenced by a signed and dated written Informed Consent form
In good physical and mental health as determined by the procedures/evaluations (completed within 14 days prior to the Induction Phase [scheduled surgical procedure])

Exclusion Criteria:

A patient will not be eligible for inclusion in this study if any of the following criteria are met:

Evidence of clinically significant cardiovascular, neuromuscular, neurological, psychiatric, renal, hepatic or pulmonary disease (including asthma), or impairment of function (as judged by the investigator)
Personal or family history of unusual sensitivity to NMBs or other agents used in surgical anesthesia
Anatomical characteristics recognized as being associated with difficult intubation conditions, even in the presence of complete jaw and vocal cord relaxation
History or evidence of vocal cord polyps and/or paralysis
History or evidence of narrow angle glaucoma
Personal or family history of malignant hyperthermia
History of major thermal injury that required hospitalization
Presence of genetically determined disorders of plasma cholinesterase, as determined by medical history
History or current evidence of abuse of any drug substance, licit or illicit (including alcohol)
Exposure to any of the following agents within 48 hours prior to the Induction Phase of the study, or, if expected to be administered within the first 15 minutes after administration of study treatment: antibiotics (except penicillins, cephalosporins, and tetracyclines), i.v. lidocaine (except i.v. lidocaine administered in conjunction with propofol to reduce local irritation), quinidine, trimetaphan, or dexamethasone.
Exposure to any of the following agents within 7 days prior to the Induction Phase of the study: tricyclic antidepressants, phenothiazines, anticonvulsants, antihistamines (H1 - or H2 - receptor antagonists), antihypertensives, antiarrhythmics (including procainamide), beta blockers (including propranolol, calcium channel blockers), diuretics (including furosemide, thiazides, mannitol, and acetazolamide), potent narcotics (including, but not limited to, oxycodone, methadone, morphine, buprenorphine, hydromorphone), and magnesium or lithium salts. Note: weak opioids including, but not limited to, propoxyphene, tramadol, hydrocodone, codeine, meperidine, and tilidine are not reasons for exclusion provided no changes in daily dosage have occurred within 3 days prior to the Induction Phase of the study.
Exposure to monoamine oxidase inhibitors within 14 days prior to the Induction Phase of the study.
Exposure to anticholinesterase or cholinomimetic agents within 30 days prior to the Induction Phase
Previous entry into this or any other study of gantacurium chloride for injection, or participation in any other investigational drug, biologic, or medical device study within 30 days prior to the Induction Phase
Pregnant (positive pregnancy test during Screening) or breastfeeding/donating breast milk
Any other condition that, in the opinion of the investigator, would jeopardize the safety or rights of a subject participating in the trial or would render the subject unable to comply with the protocol