Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C19H21N3O |
| Molecular Weight | 307.3895 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)C(=O)CC1=C(N=C2C=CC(C)=CN12)C3=CC=C(C)C=C3
InChI
InChIKey=ZAFYATHCZYHLPB-UHFFFAOYSA-N
InChI=1S/C19H21N3O/c1-13-5-8-15(9-6-13)19-16(11-18(23)21(3)4)22-12-14(2)7-10-17(22)20-19/h5-10,12H,11H2,1-4H3
| Molecular Formula | C19H21N3O |
| Molecular Weight | 307.3895 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Zolpidem is usually used for the treatment of insomnia as a hypnotic drug. It was also suggested to be effective in the treatment of dystonia in some studies. Zolpidem can be one of useful alternative pharmacological treatments for blepharospasm. Zolpidem interacts with a GABA-BZ receptor complex and shares some of the pharmacological properties of the benzodiazepines. In contrast to the benzodiazepines, which non-selectively bind to and activate all BZ receptor subtypes, zolpidem in vitro binds the BZ1 receptor preferentially with a high affinity ratio of the α1/α5 subunits. This selective binding of zolpidem on the BZ1 receptor is not absolute, but it may explain the relative absence of myorelaxant and anticonvulsant effects in animal studies as well as the preservation of deep sleep in human studies of zolpidem tartrate at hypnotic doses.
CNS Activity
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2095172 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22922343 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | AMBIEN Approved UseAmbien (zolpidem tartrate) is indicated for the short-term treatment of insomnia characterized by difficulties with sleep initiation. Ambien has been shown to decrease sleep latency for up to 35 days in controlled clinical studies [see Clinical Studies (14) Launch Date1992 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
59 ng/mL |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
ZOLPIDEM plasma | Homo sapiens population: HEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
|
121 ng/mL |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
ZOLPIDEM plasma | Homo sapiens population: HEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
26 h |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
ZOLPIDEM plasma | Homo sapiens population: HEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
|
2.5 h |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
ZOLPIDEM plasma | Homo sapiens population: HEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
Funbound
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
7.5% |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
ZOLPIDEM plasma | Homo sapiens population: HEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
|
7.5% |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
ZOLPIDEM plasma | Homo sapiens population: HEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
0.5 mg/kg single, oral Highest studied dose Dose: 0.5 mg/kg Route: oral Route: single Dose: 0.5 mg/kg Sources: |
unhealthy, 2 - 12 years Health Status: unhealthy Age Group: 2 - 12 years Sex: M+F Sources: |
Other AEs: Psychiatric symptom, Gastrointestinal disorder (NOS)... Other AEs: Psychiatric symptom (6 patients) Sources: Gastrointestinal disorder (NOS) (6 patients) Nervous system disorder NOS (5 patients) |
300 mg single, oral Overdose |
unhealthy, 68 years |
Disc. AE: Death... AEs leading to discontinuation/dose reduction: Death (grade 5, 1 patient) Sources: |
50 mg 1 times / day steady, oral Highest studied dose Dose: 50 mg, 1 times / day Route: oral Route: steady Dose: 50 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
Disc. AE: Drowsiness, Vertigo... AEs leading to discontinuation/dose reduction: Drowsiness (1.1%) Sources: Vertigo (0.8%) Amnesia (0.5%) Nausea (0.5%) Headache (0.4%) Fall (0.4%) |
90 mg 1 times / day steady, oral Highest studied dose Dose: 90 mg, 1 times / day Route: oral Route: steady Dose: 90 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
Disc. AE: Drowsiness, Dizziness... AEs leading to discontinuation/dose reduction: Drowsiness (0.5%) Sources: Dizziness (0.4%) Headache (0.5%) Nausea (0.6%) Vomiting (0.5%) |
600 mg single, oral Overdose |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
Disc. AE: Death... AEs leading to discontinuation/dose reduction: Death (grade 5, 10 patients) Sources: |
600 mg single, oral Overdose |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
Disc. AE: Somnolence, Coma... AEs leading to discontinuation/dose reduction: Somnolence (100%) Sources: Coma (1 patient) |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Nervous system disorder NOS | 5 patients | 0.5 mg/kg single, oral Highest studied dose Dose: 0.5 mg/kg Route: oral Route: single Dose: 0.5 mg/kg Sources: |
unhealthy, 2 - 12 years Health Status: unhealthy Age Group: 2 - 12 years Sex: M+F Sources: |
| Gastrointestinal disorder (NOS) | 6 patients | 0.5 mg/kg single, oral Highest studied dose Dose: 0.5 mg/kg Route: oral Route: single Dose: 0.5 mg/kg Sources: |
unhealthy, 2 - 12 years Health Status: unhealthy Age Group: 2 - 12 years Sex: M+F Sources: |
| Psychiatric symptom | 6 patients | 0.5 mg/kg single, oral Highest studied dose Dose: 0.5 mg/kg Route: oral Route: single Dose: 0.5 mg/kg Sources: |
unhealthy, 2 - 12 years Health Status: unhealthy Age Group: 2 - 12 years Sex: M+F Sources: |
| Death | grade 5, 1 patient Disc. AE |
300 mg single, oral Overdose |
unhealthy, 68 years |
| Fall | 0.4% Disc. AE |
50 mg 1 times / day steady, oral Highest studied dose Dose: 50 mg, 1 times / day Route: oral Route: steady Dose: 50 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Headache | 0.4% Disc. AE |
50 mg 1 times / day steady, oral Highest studied dose Dose: 50 mg, 1 times / day Route: oral Route: steady Dose: 50 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Amnesia | 0.5% Disc. AE |
50 mg 1 times / day steady, oral Highest studied dose Dose: 50 mg, 1 times / day Route: oral Route: steady Dose: 50 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Nausea | 0.5% Disc. AE |
50 mg 1 times / day steady, oral Highest studied dose Dose: 50 mg, 1 times / day Route: oral Route: steady Dose: 50 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Vertigo | 0.8% Disc. AE |
50 mg 1 times / day steady, oral Highest studied dose Dose: 50 mg, 1 times / day Route: oral Route: steady Dose: 50 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Drowsiness | 1.1% Disc. AE |
50 mg 1 times / day steady, oral Highest studied dose Dose: 50 mg, 1 times / day Route: oral Route: steady Dose: 50 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Dizziness | 0.4% Disc. AE |
90 mg 1 times / day steady, oral Highest studied dose Dose: 90 mg, 1 times / day Route: oral Route: steady Dose: 90 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Drowsiness | 0.5% Disc. AE |
90 mg 1 times / day steady, oral Highest studied dose Dose: 90 mg, 1 times / day Route: oral Route: steady Dose: 90 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Headache | 0.5% Disc. AE |
90 mg 1 times / day steady, oral Highest studied dose Dose: 90 mg, 1 times / day Route: oral Route: steady Dose: 90 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Vomiting | 0.5% Disc. AE |
90 mg 1 times / day steady, oral Highest studied dose Dose: 90 mg, 1 times / day Route: oral Route: steady Dose: 90 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Nausea | 0.6% Disc. AE |
90 mg 1 times / day steady, oral Highest studied dose Dose: 90 mg, 1 times / day Route: oral Route: steady Dose: 90 mg, 1 times / day Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Death | grade 5, 10 patients Disc. AE |
600 mg single, oral Overdose |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Coma | 1 patient Disc. AE |
600 mg single, oral Overdose |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Somnolence | 100% Disc. AE |
600 mg single, oral Overdose |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| no | ||||
| no | ||||
| no | ||||
| no | ||||
| weak [IC50 99 uM] | ||||
| weak | ||||
| weak |
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| yes | ||||
| yes | ||||
| yes | ||||
| yes | ||||
| yes | yes (co-administration study) Comment: A single-dose interaction study with zolpidem tartrate 10 mg and rifampin (CYP3A4 inducer) 600 mg at steady-state levels in female subjects showed significant reductions of the AUC (-73%), Cmax (-58%), and T1/2 (-36 %) of zolpidem together |
Tox targets
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
PubMed
| Title | Date | PubMed |
|---|---|---|
| Relation between discriminative and reinforcing effects of midazolam, pentobarbital, chlordiazepoxide, zolpidem, and imidazenil in baboons. | 2002-10 |
|
| Functional characterization of GABA(A) receptors in neonatal hypothalamic brain slice. | 2002-10 |
|
| Zolpidem pharmacokinetic properties in young females: influence of smoking and oral contraceptive use. | 2002-10 |
|
| Comparison of the effects of zaleplon, zolpidem, and triazolam at various GABA(A) receptor subtypes. | 2002-09-13 |
|
| [Abuse, tolerance and dependence of zolpidem: three case reports]. | 2002-09-10 |
|
| Relative picrotoxin insensitivity distinguishes ionotropic GABA receptor-mediated IPSCs in hippocampal interneurons. | 2002-09 |
|
| GABA(A) receptor alpha-1 subunit deletion alters receptor subtype assembly, pharmacological and behavioral responses to benzodiazepines and zolpidem. | 2002-09 |
|
| Mechanisms of anabolic androgenic steroid modulation of alpha(1)beta(3)gamma(2L) GABA(A) receptors. | 2002-09 |
|
| Sleep disorders and daytime sleepiness in state police shiftworkers. | 2002-08-27 |
|
| The heterogeneity of central benzodiazepine receptor subtypes in the human hippocampal formation, frontal cortex and cerebellum using [3H]flumazenil and zolpidem. | 2002-08-15 |
|
| Severe impairment of NMDA receptor function in mice carrying targeted point mutations in the glycine binding site results in drug-resistant nonhabituating hyperactivity. | 2002-08-01 |
|
| Hallucinations and Zolpidem. | 2002-08 |
|
| Imaging the GABA-benzodiazepine receptor subtype containing the alpha5-subunit in vivo with [11C]Ro15 4513 positron emission tomography. | 2002-07 |
|
| Early cerebral activities of the environmental estrogen bisphenol A appear to act via the somatostatin receptor subtype sst(2). | 2002-06 |
|
| Zolpidem, vascular headache, and hallucinations in an adolescent. | 2002-06 |
|
| Adaptive time-frequency parametrization in pharmaco EEG. | 2002-05-30 |
|
| [Epileptic seizures as a sign of abstinence from chronic consumption of zolpidem]. | 2002-05-22 |
|
| Rifampin and rifabutin drug interactions: an update. | 2002-05-13 |
|
| Long term benzodiazepine use for insomnia in patients over the age of 60: discordance of patient and physician perceptions. | 2002-05-08 |
|
| Anxiolytic-like effects of acute and chronic GABA transporter inhibition in rats. | 2002-05 |
|
| Role of GABAA/benzodiazepine receptors containing alpha 1 and alpha 5 subunits in the discriminative stimulus effects of triazolam in squirrel monkeys. | 2002-05 |
|
| Selective modulation of tonic and phasic inhibitions in dentate gyrus granule cells. | 2002-05 |
|
| GABAA-benzodiazepine receptor complex ligands and stress-induced hyperthermia in singly housed mice. | 2002-05 |
|
| [Unexplained increase in aminotransferases and obstructive sleep apnea syndrome]. | 2002-04 |
|
| Clinical syndrome associated with zolpidem ingestion in dogs: 33 cases (January 1998-July 2000). | 2002-03-20 |
|
| "As needed" pharmacotherapy combined with stimulus control treatment in chronic insomnia--assessment of a novel intervention strategy in a primary care setting. | 2002-03 |
|
| The effect of zolpidem on operant behavior and its relation to pharmacokinetics after intravenous and subcutaneous administration: concentration-effect relations. | 2002-03 |
|
| Soyka M, Bottlender R, Möller H-J; Epidemiological evidence for a low abuse potential of zolpidem; Pharmacopsychiatry 2000, 33: 138 - 141. | 2002-03 |
|
| Selective actions on sleep or anxiety by exploiting GABA-A/benzodiazepine receptor subtypes. | 2002-03 |
|
| Zolpidem in progressive supranuclear palsy. | 2002-03 |
|
| Zolpidem improves dystonia in "Lubag" or X-linked dystonia-parkinsonism syndrome. | 2002-02-26 |
|
| Mechanism of alpha-subunit selectivity of benzodiazepine pharmacology at gamma-aminobutyric acid type A receptors. | 2002-02-15 |
|
| [Pharmacological profile and clinical effect of zolpidem (Myslee tablets), a hypnotic agent]. | 2002-02 |
|
| Discriminative stimulus effects of benzodiazepine (BZ)(1) receptor-selective ligands in rhesus monkeys. | 2002-02 |
|
| Changes in GABA(A) receptor gene expression induced by withdrawal of, but not by long-term exposure to, zaleplon or zolpidem. | 2002-02 |
|
| Fibromyalgia: patient perspectives on symptoms, symptom management, and provider utilization. | 2002-01 |
|
| Continuous versus non-nightly use of zolpidem in chronic insomnia: results of a large-scale, double-blind, randomized, outpatient study. | 2002-01 |
|
| Comparative meta-analysis of pharmacotherapy and behavior therapy for persistent insomnia. | 2002-01 |
|
| Zolpidem in restless legs syndrome. | 2002 |
|
| Tolerability of hypnosedatives in older patients. | 2002 |
|
| Melatonin for the prevention and treatment of jet lag. | 2002 |
|
| Diminished allopregnanolone enhancement of GABA(A) receptor currents in a rat model of chronic temporal lobe epilepsy. | 2001-12-01 |
|
| Zolpidem use and hip fractures in older people. | 2001-12 |
|
| Assessing the effects of an intervention by a pharmacist on prescribing and administration of hypnotics in nursing homes. | 2001-12 |
|
| Delirium associated with zolpidem. | 2001-12 |
|
| [Zolpidem: the risk of tolerance and dependence according to case reports, systematic studies and recent molecularbiological data]. | 2001-12 |
|
| Arousal from a semi-comatose state on zolpidem. | 2001-10 |
|
| WHO Expert Committee on Drug Dependence. Thirty-second report. | 2001 |
|
| Development and modulation of GABA(A) receptor-mediated neurotransmission in the CA1 region of prenatally protein malnourished rats. | 2001 |
|
| [Correction of sleep disorders and efficacy of antihypertensive monotherapy in elderly patients: use of ivadal]. | 2001 |
Patents
Sample Use Guides
Dosage in Adults: the recommended initial dose is 5 mg for women and either 5 or 10 mg for men, taken only once per night immediately before bedtime with at least 7-8 hours remaining before the planned time of awakening. If the 5 mg dose is not effective, the dose can be increased to 10 mg. In some patients, the higher morning blood levels following use of the 10 mg dose increase the risk of next day impairment of driving and other activities that require full alertness. The total dose of AMBIEN (zolpidem tartrate) should not exceed 10 mg once daily immediately before bedtime. Ambien should be taken as a single dose and should not be readministered during the same night.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22922343
Human embryonic kidney (HEK) 293 cells stably expressing recombinant α1β2γ2s GABA(A) receptors were exposed to zolpidem (1 and 10 μmol/L) for short-term (2 h daily for 1, 2, or 3 consecutive days) or long-term (continuously for 48 h). Radioligand binding studies were used to determine the parameters of [(3)H]flunitrazepam binding sites. A single (2 h) or repeated (2 h daily for 2 or 3 d) short-term exposure to zolpidem affected neither the maximum number of [(3)H]flunitrazepam binding sites nor the affinity. In both control and short-term zolpidem treated groups, addition of GABA (1 nmol/L-1 mmol/L) enhanced [(3)H]flunitrazepam binding in a concentration-dependent manner. The maximum enhancement of [(3)H]flunitrazepam binding in short-term zolpidem treated group was not significantly different from that in the control group. In contrast, long-term exposure to zolpidem resulted in significantly increase in the maximum number of [(3)H]flunitrazepam binding sites without changing the affinity. Furthermore, long-term exposure to zolpidem significantly decreased the ability of GABA to stimulate [(3)H]flunitrazepam binding.
| Substance Class |
Chemical
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| Record UNII |
7K383OQI23
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Validated (UNII)
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WHO-VATC |
QN05CF02
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NDF-RT |
N0000175759
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DEA NO. |
2783
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WHO-ATC |
N05CF02
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C29756
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LIVERTOX |
NBK547962
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C62000
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TRANSPORTER -> NON-INHIBITOR |
IC50
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METABOLIC ENZYME -> SUBSTRATE |
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TARGET -> AGONIST |
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SALT/SOLVATE -> PARENT |
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SALT/SOLVATE -> PARENT |
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BINDER->LIGAND |
BINDING
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SALT/SOLVATE -> PARENT |
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METABOLIC ENZYME -> SUBSTRATE |
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METABOLIC ENZYME -> SUBSTRATE | |||
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SALT/SOLVATE -> PARENT |
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METABOLIC ENZYME -> SUBSTRATE |
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METABOLIC ENZYME -> SUBSTRATE |
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METABOLITE INACTIVE -> PARENT |
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METABOLITE -> PARENT |
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METABOLITE INACTIVE -> PARENT |
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METABOLITE INACTIVE -> PARENT |
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METABOLITE -> PARENT |
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ACTIVE MOIETY |
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| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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| Route of Elimination | PHARMACOKINETIC |
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| MAXIMUM TOLERATED DOSE | TOXICITY |
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ORAL SPRAY, SL TABLET |
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| Route of Elimination | PHARMACOKINETIC |
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| ORAL BIOAVAILABILITY | PHARMACOKINETIC |
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| Biological Half-life | PHARMACOKINETIC |
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SPECIAL POPULATIONS PHARMACOKINETIC PHARMACOKINETIC PHARMACOKINETIC PHARMACOKINETIC |
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| Volume of Distribution | PHARMACOKINETIC |
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SPECIAL POPULATIONS PHARMACOKINETIC PHARMACOKINETIC PHARMACOKINETIC |
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