Phase 1 Study of JADE101 in Healthy Japanese and Chinese Participants
This study is testing a single dose of JADE101, given as an injection under the skin, in healthy Japanese and Chinese volunteers. The main goals are to see how safe JADE101 is and if people can tolerate it well. Researchers will also look at how the body processes JADE101. You may be able to join if you are a healthy Japanese or Chinese person between 18 and 55 years old, born in Japan or China, and meet specific weight and BMI requirements. The study aims to enroll 40 participants, but its current recruitment status is unclear.
- Study design
- This is a Phase 1 interventional study. It will involve a single dose of JADE101 and plans to enroll 40 healthy participants.
- What's involved
- You would need to comply with study site stays, scheduled visits, and study procedures. The study will monitor you from Day 1 through 48 weeks.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for safety and tolerability from Day 1 through 48 weeks after receiving JADE101.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
A Single Dose, Phase 1 Study of JADE101 in Healthy Japanese and Chinese Participants
At a glance
Conditions
NCT07525947
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Parexel Early Phase Clinical Unit (EPCU)
Glendale, Californiastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Li Li, MD · STUDY_DIRECTOR · Jade Biosciences
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Safety and tolerability of single dose of JADE101 in healthy Japanese and Chinese participantsDay 1 through 48 weeks
Incidence of treatment-emergent adverse events
- CmaxDay 1 through 48 weeks
Maximum observed serum concentration
- TmaxDay 1 through 48 weeks
Time to reach Cmax
- AUClastDay 1 through 48 weeks
The area under the concentration-time curve from time zero to the time of the last observed quantifiable (non-zero) concentration
- T1/2Day 1 through 48 weeks
Apparent first-order terminal elimination half-life