A Single Dose, Phase 1 Study of JADE101 in Healthy Japanese and Chinese Participants
← catalyst calendarNCT07525947 · readout ≤ 285 d
Sponsored by Jade Biosciences, Inc. (industry) · JBIO — their whole pipeline →.
Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Basic science
Enrollment
40estimated
Sites
1
Country
United States
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-05-01 | actual | When the study began enrolling |
| Primary completion | May 2027 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | May 2027 | estimated | The whole study's end, after follow-up |
| First posted | 2026-04-13 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-06-04 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Healthy Volunteers (HV)
Intervention
- Drug: JADE101
Primary outcomes
what the primary-completion date above is the date OFSafety and tolerability of single dose of JADE101 in healthy Japanese and Chinese participants
measured Day 1 through 48 weeks
Cmax
measured Day 1 through 48 weeks
Tmax
measured Day 1 through 48 weeks
AUClast
measured Day 1 through 48 weeks
T1/2
measured Day 1 through 48 weeks
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