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NCT07455084Not yet recruitingPhase 1

A Study to Detect the Radioactivity of 14C-SEP-380135 in Urine and Feces in Healthy Male Adults

A Phase 1 Trial to Assess the Mass Balance and Pharmacokinetics of a Single Oral Administration of 14C-SEP-380135 in Healthy Male Adults

Source: ClinicalTrials.gov · Last updated 16 Oct 2026

Brief summary (registry, in English)

The purpose of the present trial is to obtain information on the absorption, distribution, metabolism, excretion and pharmacokinetics (PK) of 14C-SEP-380135 and its metabolites following a single oral dose.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
8 (estimated)
First submitted
3 Mar 2026
Start date
1 Nov 2026
Primary completion date
2 Dec 2026
Lead sponsor
Otsuka Pharmaceutical Development & Commercialization, Inc.
NCT number
NCT07455084

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 8
  • From 1 Nov 2026 to the primary completion date, 2 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Have taken an investigational drug within 30 days or 5 half-lives, if known, (whichever is longer) prior to screening.
  • Have had prior exposure to SEP-380135.
  • Attempted suicide within 12 months prior to screening.

Lab values

  • A history of sick sinus syndrome, any degree of atrioventricular block, Heart attack (myocardial infarction), heart failure (NYHA Class II-IV), cardiomyopathy, pulmonary congestion, cardiac arrhythmias, prolonged QT interval, congenital long QT syndrome, family history of long QT, or moderate to severe hypokalemia. A participant with non-clinically significant ECG abnormalities at screening and check-in requires approval from the medical monitor and the sponsor's physician.

Other

  • Are currently participating in another clinical trial.
  • Are predicted poor metabolizer CYP2D6 phenotypes. Note: Other protocol-specified inclusion/exclusion criteria may apply.

Who the study is looking for

  • Body mass index (BMI) between 18.0 and 32.0 kilograms per square meter (kg/m²).
  • In good overall health, based on:
    • Medical history
    • Physical examination
    • Neurological examination
    • Vital signs
    • Electrocardiogram (ECG)
    • Blood and urine tests (serum chemistry, hematology, urinalysis, serology)
  • Regular daily bowel movements (at least one per day) for 30 days before Day -2.
  • Ability to provide written informed consent and follow all study instructions.
  • Has a stable living situation at screening and agrees to return to a similar living arrangement after the in-clinic stay.

Age in the registry: 18 years to 55 years · Sex: Male · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Celerion, Inc.
Coordinator of this site? Confirm its status
LincolnUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.