A Study of Acetaminophen/Naproxen Sodium Fixed Combination Tablets in Adolescents 12 to <17 Years of Age With Pain
Study Details
Study Description
Brief Summary
The purpose of this study is to investigate the population pharmacokinetics of acetaminophen and naproxen from a novel acetaminophen /naproxen sodium fixed combination tablet in adolescents 12 to less than (<) 17 years of age with post-procedure orthodontic pain and to describe the effect of subject-specific covariates, including age and body weight, on inter-subject variability in acetaminophen and naproxen pharmacokinetics in adolescents 12 to <17 years of age with post-procedure orthodontic pain.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Acetaminophen /Naproxen Sodium Participants with age group 12 to less than (<) 17 years who undergone a non-surgical orthodontic procedure will enroll and receive fixed dose combination of acetaminophen/naproxen sodium tablet orally on baseline (Day 0). |
Drug: Acetaminophen/Naproxen Sodium
Fixed dose combination of acetaminophen/naproxen sodium tablet will be administered orally.
|
Outcome Measures
Primary Outcome Measures
- Apparent Clearance (CL/F) of Acetaminophen/Naproxen Sodium [Pre-dose up to 48 hours post dose]
CL/F is defined as apparent clearance of acetaminophen/naproxen sodium.
- Apparent Central Volume of Distribution (Vc/F) After Oral Dosing of Acetaminophen/Naproxen Sodium [Pre-dose up to 48 hours post dose]
Vc/F is defined as apparent central volume of distribution after oral dosing of acetaminophen/naproxen sodium.
- Apparent Peripheral Volume of Distribution (Vp/F) After Oral Dosing of Acetaminophen/Naproxen Sodium [Pre-dose up to 48 hours post dose]
Vp/F is defined as apparent peripheral volume of distribution after oral dosing of acetaminophen/naproxen sodium.
- Apparent Inter-compartmental Clearance (Q/F) of Acetaminophen/Naproxen Sodium [Pre-dose up to 48 hours post dose]
Q/F is defined as apparent inter-compartmental clearance of acetaminophen/naproxen sodium.
- First-order Absorption Rate Constant (Ka) of Acetaminophen/Naproxen Sodium [Pre-dose up to 48 hours post dose]
Ka is defined as first-order absorption rate constant of acetaminophen/naproxen sodium.
- Maximum Plasma Concentration (Cmax) of Acetaminophen/Naproxen Sodium [Pre-dose up to 48 hours post dose]
Cmax is defined as maximum plasma concentration of acetaminophen/naproxen sodium.
- Time of occurrence of Maximum Plasma Concentration (Tmax) of Acetaminophen/Naproxen Sodium [Pre-dose up to 48 hours post dose]
Tmax is defined as time of occurrence of maximum plasma concentration of acetaminophen/naproxen sodium.
- Area Under the Plasma Concentration versus Time Curve from Start of Drug Administration Until the Time of the Last Measurable Plasma Concentration (AUC[0-t]) [Pre-dose up to 48 hours post dose]
AUC(0-t) is defined as area under the plasma concentration versus time curve from start of drug administration until the time of the last measurable plasma concentration of acetaminophen/naproxen sodium.
- Area Under the Plasma Concentration versus Time Curve From Start of Drug Administration Until Infinity (AUC[0-infinite]) [Pre-dose up to 48 hours post dose]
AUC(0-infinite) is defined as area under the plasma concentration versus time curve from start of drug administration until infinity of acetaminophen/naproxen sodium.
- Terminal Elimination Rate Constant (lambda[z]) of Acetaminophen/Naproxen Sodium [Pre-dose up to 48 hours post dose]
Lambda(z) is defined as terminal elimination rate constant of acetaminophen/naproxen sodium.
- Half Life (t1/2) of Acetaminophen/Naproxen Sodium [Pre-dose up to 48 hours post dose]
T1/2 is defined as half life of acetaminophen/naproxen sodium.
Secondary Outcome Measures
- Number of Participants with Adverse Events (AEs) [Up to 3 days]
An AE is any untoward medical occurrence that occurs in participants after they have signed an informed consent for the study. The event does not need to have a suspected causal relationship with the investigational product (IP).
Eligibility Criteria
Criteria
Inclusion Criteria:
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A parent or a legal guardian of the participant has signed and dated the informed consent document and a written assent has been signed by the participant
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Has undergone an orthodontic procedure within 72 hours prior to dosing
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Is otherwise a healthy adolescent between the ages of 12 to less than (<) 17 years at baseline (dosing). Health is defined as the absence of clinically relevant abnormalities as judged by the principle investigator (PI) on the basis of a detailed medical history, physical examination, blood pressure, respiratory rate and pulse rate measurements, and clinical laboratory tests. The responsible PI may request additional investigations or analyses if necessary
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Has a minimum weight of 72 pounds and has a Body Mass Index (BMI) between the 5th and 95th percentile for their age at dosing
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Has been fasted for at least 10 hours prior to dose administration of the investigational product
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Is a non-tobacco user or previous user who completely stopped smoking or using any form of tobacco or nicotine-containing product [including e-cigarettes, cigarettes, non-combusted cigarettes, cigars, smokeless tobacco (such as dip, snuff, snus, and chewing tobacco)] for at least 12 months before screening visit of this study
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If female, have a negative test for pregnancy at screening and baseline (dosing)
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Females of childbearing potential and males agree to the contraceptive requirements
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Is able to comprehend the requirements of the study (based upon clinical site personnel's assessment) and is willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures specified within the protocol
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Are willing for investigational product of this study to be the only analgesic product used during the study
Exclusion Criteria:
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Use of prescription or non-prescription medications within a period less than 5 half-lives before the first investigational product (IP) administration unless these are contraceptives or occasional use of other medications approved by the Investigator
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Use of Ibuprofen within 6 hours prior to the dose administration of the investigational product
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Use of any vitamins, dietary and herbal supplements within seven days before first dose of study drug
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Has hypersensitivity to acetaminophen, naproxen, other non-steroidal anti-inflammatory drug (NSAIDs), including acetylsalicylic acid, or to any of the ingredients
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If female, has a positive pregnancy test or is breast-feeding or currently trying to become pregnant
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Has a positive test for human immunodeficiency virus (HIV) 1 and 2 antibodies, hepatitis B surface antigen (HBsAg), or hepatitis C antibodies (anti-HCV)
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Has a positive test for drugs of abuse at screening or baseline (dosing)
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Has difficult venipuncture access and/or refuses to undergo venipuncture
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Has clinically significant renal or hepatic impairment according to the medically qualified Investigator discretion, or presence of a disease, which in the opinion of the Investigator, would preclude the use of IP
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Has a history of peptic ulcers, gastrointestinal bleeding of any etiology, bleeding disorders, gastrointestinal disease (including chronic heartburn or gastroesophageal reflux disease, or any other active inflammatory disease of the gastrointestinal tract such as ulcerative colitis or crohn's disease), or has a history of gastrointestinal surgery (including cholecystectomy) that would affect the pharmacokinetic (PK) assessment of the drug or the safety of the participant
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Has history of substance abuse, as judged by the PI, within 12 months preceding this study
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Has used alcohol within 24 hours of baseline visit and/or has positive alcohol test in expired air at screening or baseline visit
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Has used food or beverages containing xanthines (that is, tea, coffee, cola drinks, energy drinks or chocolate) for 48 hours prior to the dosing and during the study period
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Has used grapefruit and savoy oranges for 48 hours prior to the dosing and during the study period
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Participating in a clinical trial and/or treated with any investigational product within 3 months preceding the dose of study drug
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Has preplanned surgery, procedures, or personal commitments that would interfere with the conduct of the study
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Had an acute blood loss of 50 milliliter (mL) to 249 mL within the 30 days, or 250 mL to 449 mL within the 45 days, or greater than or equal to (>=) 450 mL within the 60 days before first dose administration
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Has any acute or chronic medical or psychiatric condition(s) that may increase the risk associated with study participation or IP administration or may interfere with the interpretation of study results and, in the judgment of the medically qualified Investigator, would make the participant inappropriate for entry into this study
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Has any clinically important abnormal value for serum chemistry, hematology, or urinalysis at screening. Laboratory values will generally be within the normal ranges, although minor deviations in tests (except those explicitly specified in the inclusion criteria) that are not considered clinically important by the Investigator are acceptable
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Is related to persons involved directly or indirectly with the conduct of the study (that is, principal investigator, sub-investigators, study coordinators, other study personnel, employees or contractors of the Sponsor or Johnson & Johnson (J&J) subsidiaries, and the family of each)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | JBR Clinical Research LLP | Salt Lake City | Utah | United States | 84107 |
Sponsors and Collaborators
- Johnson & Johnson Consumer Inc. (J&JCI)
Investigators
- Study Director: Johnson & Johnson Consumer Inc. (J&JCI) Clinical Trial, Johnson & Johnson Consumer Inc. (J&JCI)
Study Documents (Full-Text)
None provided.More Information
Publications
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