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A Study Investigating the Movement of Lu AF28996 Into, Through, and Out of the Body of Healthy Men - Trial NCT06337110

Access comprehensive clinical trial information for NCT06337110 through Pure Global AI's free database. This Phase 1 trial is sponsored by H. Lundbeck A/S and is currently Recruiting. The study focuses on Healthy Participants. Target enrollment is 8 participants.

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NCT06337110
Phase 1
Recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06337110
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A Study Investigating the Movement of Lu AF28996 Into, Through, and Out of the Body of Healthy Men
Interventional, Open-label, Single-dose Trial Investigating the Absorption, Metabolism, and Excretion (AME) of Lu AF28996 Following a Single Oral Dosing of 14C-Lu AF28996 to Healthy Men

Study Focus

Healthy Participants

Lu AF28996

Interventional

drug

Sponsor & Location

H. Lundbeck A/S

Leeds, United Kingdom

Timeline & Enrollment

Phase 1

Apr 10, 2024

May 25, 2024

8 participants

Primary Outcome

Total Recovery of the Administered Radiolabelled Drug-related Material (Percentage of Dose in Urine and Faeces),AUC0-infinity: Area Under the Plasma Concentration Curve of Radiolabelled Drug-related Material from Zero to Infinity,Cmax: Maximum Observed Plasma Concentration of Radiolabelled Drug-related Material,Tmax: Nominal Time Corresponding to the Occurrence of Cmax of Radiolabelled Drug-related Material,Tยฝ: Apparent Elimination Half-life of Radiolabelled Drug-related Material,AUC0-infinity of Lu AF28996,Cmax of Lu AF28996,Tmax of Lu AF28996,Tยฝ of Lu AF28996

Summary

The main goal of this study is to learn about how Lu AF28996 moves into, through, and out of
 the body after a single dose is given to healthy male participants.

ICD-10 Classifications

Seeking and accepting physical, nutritional and chemical interventions known to be hazardous and harmful
Healthy person accompanying sick person
Routine general health check-up of sports teams
Obesity
Persons with potential health hazards related to communicable diseases

Data Source

ClinicalTrials.gov

NCT06337110

Non-Device Trial