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Phase 4 Completed N=13 Randomized Other

Open Label Crossover Study Pharmacokinetics (PK) Study in Healthy Volunteers Receiving Various Forms of Fentanyl

Healthy
Source: ClinicalTrials.gov NCT02470390 ↗
Enrolled (actual)
13
Serious AEs
2.7%
Results posted
Mar 2018
Primary outcomePrimary: Time to Reach Maximum Observed Concentration (Tmax) of Fentanyl in Cerebrospinal Fluid (CSF) (1 of 3) — 1.01; 2.00 h
◆ Published Evidence
No publication linked

No peer-reviewed publication reporting this trial's results has been linked yet. This can indicate results are unpublished — a known publication-bias signal. We re-check periodically.

Summary

A partially randomized, open-label, 3-way crossover, single-center, systemic and CSF PK and bioavailability study in healthy volunteers.

Outcome Measures

OutcomeResultp-value
PRIMARY
Time to Reach Maximum Observed Concentration (Tmax) of Fentanyl in Cerebrospinal Fluid (CSF) (1 of 3)
1.01; 2.00
PRIMARY
Maximum Observed Concentration (Cmax) of Fentanyl in Cerebrospinal Fluid (CSF) (2 of 3)
84.54; 56.37
PRIMARY
Area Under the Concentration-Time Curve From Hour 0 to Hour 6 (AUC 0-6h) of Fentanyl in Cerebrospinal Fluid (CSF) (3 of 3)
300.25; 221.49
PRIMARY
Maximum Observed Concentration (Cmax) of Fentanyl in Plasma (1 of 5)
541.28; 369.59; 1166.51
PRIMARY
Area Under the Concentration-Time Curve From Time 0 to the Last Quantifiable Concentration (AUC 0-tlast) of Fentanyl in Plasma (2 of 5)
2752.51; 2359.08; 2236.46
PRIMARY
Area Under the Concentration-Time Curve From Time 0 Extrapolated to Infinity (AUC 0-inf) of Fentanyl in Plasma (3 of 5)
3413.80; 2879.85; 2871.89
PRIMARY
Time to Reach Maximum Observed Concentration (Tmax) of Fentanyl in Plasma (4 of 5)
0.63; 0.75; 0.07
PRIMARY
Terminal Elimination Half-Life (t1/2) of Fentanyl in Plasma (5 of 5)
12.08; 10.73; 12.25

Eligibility Criteria

Inclusion Criteria

  • Normal healthy male or female between the ages of 18 to 65 years. Never smokers or Non-smokers (cessation of smoking ≥ 6 months ago). Body Mass Index (BMI = weight/height2) greater than or equal to 18.5 kg/m2 and less than or equal to 32.0 kg/m2.

No clinically meaningful findings in the physical examination, oral and nasal examination and 12-lead electrocardiogram.

Negative for drugs of abuse, alcohol, and nicotine. Negative for hepatitis A, B, and C and Human Immunodeficiency Virus (HIV). No clinical laboratory values outside of the acceptable range, unless, in the opinion of the Principal Investigator, they are deemed not clinically significant.

Exclusion Criteria

  • Subject has a known history of allergic reaction, hypersensitivity, or clinically significant intolerance to opioids, fentanyl or components of the study drugs.
  • Subjects with a high potential for opioid addiction (personal or family history).
  • Subject is lactating or considered at risk of pregnancy. 4. Subject has impaired liver function (e.g., alanine aminotransferase [ALT] ≥ 3 times the upper limit of normal [ULN] or bilirubin ≥ 3 times ULN), known active hepatic disease (e.g., hepatitis), or evidence of clinically significant liver disease or other condition affecting the liver that may suggest the potential for an increased susceptibility to hepatic toxicity with oral diclofenac exposure.
  • Subject has any history of renal disease that, in the opinion of the investigator, would contraindicate study participation; or subject has significantly impaired renal function as evidenced by an estimated GFR of ≤60 ml/min/1.73m2.
  • Subject has a history or evidence of significant nasal pathology, including polyps or nasal obstructions.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02470390). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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