A Study to Compare the Amount of Two Forms of Tafamidis in the Blood of Healthy Adults Under Fed Conditions
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Phase
Phase 1
Status
Terminated
Study type
Interventional
Design
Randomized · None · Basic science
Enrollment
24actual
Sites
1
Country
Belgium
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
Why the sponsor stopped it
The study was terminated for business reasons; there were no safety concerns.
As filed on the registry record, in the sponsor's own words.
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-03-23 | actual | When the study began enrolling |
| Primary completion | 2026-05-12 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2026-06-02 | actual | The whole study's end, after follow-up |
| First posted | 2026-03-13 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-06-26 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Healthy
Interventions
- Drug: Tafamidis (Reference)
- Drug: Tafamidis (Test)
Primary outcomes
what the primary-completion date above is the date OFArea under the concentration-time curve (AUCinf)
measured Hour 0, 0.5, 1, 2, 3, 4, 6, 8, 12, 24, 48, 72, 96, 120, 144, 168.
Maximum observed plasma concentration (Cmax)
measured Hour 0, 0.5, 1, 2, 3, 4, 6, 8, 12, 24, 48, 72, 96, 120, 144, 168
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