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This is a randomized, double-blind, double-dummy, placebo- and active-controlled 4 period, 4 way crossover study to assess the intranasal abuse potential of manipulated ADAIR formulation in nondependent, recreational stimulant users. The study will consist of an outpatient Screening Visit, an in clinic Qualification Phase, an in-clinic Treatment Phase, and an outpatient Follow-Up visit.
VAL-104 is a phase 1, randomized, double-blind, double-dummy, placebo- and active-controlled 4 period, 4 way crossover study to assess the intranasal abuse potential of manipulated ADAIR formulation in nondependent, recreational stimulant users. The study objectives include assessing the pharmacodynamics (PD), pharmacokinetics (PK), safety and tolerability of manipulated ADAIR 30mg when compared to crushed d-amphetamine sulfate and placebo. The primary PD endpoint is mean maximum drug liking (Emax) on a bipolar 100mm visual analog scale.
A total of 64 subjects demonstrating a confirmed positive response to stimulants will enter the treatment phase. Safety will be assess via adverse events, vital signs, ECGs, clinical laboratory tests and Columbia Suicide Severity Rating Scale (C-SSRS).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Oral Placebo + Intranasal manipulated ADAIR | Experimental | Oral Placebo + Intranasal manipulated ADAIR 30 mg |
|
| Oral Placebo + Intranasal crushed dextroamphetamine sulfate | Active Comparator | Oral Placebo + Intranasal crushed dextroamphetamine sulfate IR 30 mg |
|
| Oral ADAIR + Intranasal Placebo | Experimental | Oral ADAIR 30 mg + Intranasal Placebo |
|
| Oral Placebo + Intranasal Placebo | Placebo Comparator | Oral Placebo + Intranasal Placebo |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ADAIR 10 mg IR tablets | Drug | manipulated ADAIR 3x10mg |
|
| Measure | Description | Time Frame |
|---|---|---|
| Drug Liking Emax Visual Analog Scale (VAS) | Peak effect for drug liking based on bipolar VAS from 0-100 scale | Up to 24 hours post-dose |
| Measure | Description | Time Frame |
|---|---|---|
| Take Drug Again Emax VAS | Peak effect for take drug again based on bipolar VAS from 0-100 scale | Up to 24 hours post dose |
| Overall Drug Liking Emax VAS | Peak effect for overall drug liking based on bipolar VAS from 0-100 scale |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Timothy Whitaker, M | Vallon Pharmaceuticals, Inc. | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Vallon Investigational Site | Salt Lake City | Utah | 84124 | United States |
Currently there is no IPD plan
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| d-amphetamine sulfate | Drug | crushed d-amphetamine sulfate 3x10mg |
|
|
| Placebo | Drug | placebo for oral and intranasal administration |
|
| Up to 24 hours post dose |
| Plasma concentrations (PK parameters) | plasma concentrations of ADAIR and dextroamphetamine sulfate | Up to 36 hours post dose |
| Safety (adverse events) | Incidence of adverse events | Day 1 to Day 18 |
| ID | Term |
|---|---|
| D001289 | Attention Deficit Disorder with Hyperactivity |
| D009290 | Narcolepsy |
| ID | Term |
|---|---|
| D019958 | Attention Deficit and Disruptive Behavior Disorders |
| D065886 | Neurodevelopmental Disorders |
| D001523 | Mental Disorders |
| D006970 | Disorders of Excessive Somnolence |
| D020919 | Sleep Disorders, Intrinsic |
| D020920 | Dyssomnias |
| D012893 | Sleep Wake Disorders |
| D009422 | Nervous System Diseases |
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| ID | Term |
|---|---|
| D003913 | Dextroamphetamine |
| ID | Term |
|---|---|
| D000661 | Amphetamine |
| D000662 | Amphetamines |
| D010627 | Phenethylamines |
| D005021 | Ethylamines |
| D000588 | Amines |
| D009930 | Organic Chemicals |
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