CompletedPhase 1ketamine

KF2024#1-trial: Esketamine Interaction Study

Sponsored by Helsinki University Central Hospital

NCT ID
NCT06726382
Target Enrollment
12 participants
Start Date
2024-12-09
Est. Completion
2025-04-29

About This Study

Esketamine is a drug which is used for depression treatment, to relieve pain and, in larger doses, in anesthesia. Spravato nasal spray is the only esketamine product on the market used for the treatment of depression, but the high price limits the use of the drug. The aim of this study is to compare the concentration of esketamine after nasal (licensed product Spravato) and oral administration with and without a CYP3A4 inhibitor. Grapefruit juice and cobicistat are studied as CYP3A4 inhibitors in the study. In an open four-phase, randomized, alternating study with 12 healthy volunteers, the subjects will receive Spravato 28 mg nasal or esketamine 28 mg oral with either grapefruit juice, cobicistat or water in the study facilities. Blood samples will be collected and esketamine pharmacokinetics will be monitored up to 24 hours postdose. Primary endpoint is area under the plasma concentration-time curve of esketamine.

Conditions Studied

Drug InteractionsFood-drug Interaction

Interventions

  • Esketamine Nasal Spray
  • Esketamine 28 mg
  • Cobicistat 150 MG
  • Grapefruit juice

Eligibility

Age:18 Years - 45 Years
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria:

* signed consent
* age 18-45 years
* healthy
* no indications of substance abuse
* Accepted results from laboratory tests (blood hemoglobin, basic blood count and blood platelets, alanine aminotransferase, alkaline phosphatase, glutamyl transferase, creatinine, plasma potassium and sodium). Negative pregnancy test result (serum human chorionic gonadotropin) for women.
* no significant abnormalities in the ECG
* systolic blood pressure 140 mmHg-100 mmHg
* heart rate ≥50/minute

Exclusion Criteria:

* significant illness
* less than 3 months since the last clinical trial
* less than 3 months after donating blood
* significant overweight/poor veins
* BMI below 18.5 kg/m2
* past or present mood disorder or suicidality
* substance abuse
* systolic blood pressure below 100 mmHg or above 140 mmHg
* heart rate \<50/minute
* conduction disorder or other significant abnormality in the ECG
* smoking
* regular medication (including e-pills and other preparations containing estrogens)
* pregnancy or its planning or breastfeeding
* hypersensitivity to investigational drugs or excipients of medicinal products
* use of natural products (such as St. John's wort)

Study Locations (1)

Department of Clinical Pharmacology
Helsinki, Finland

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source