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Safety, Tolerability, and Pharmacokinetics of Multiple Dose Combinations of SION-451 and Complementary Modulators SION-2222 and SION-109 in Healthy Participants.

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NCT07035990

Sponsored by Sionna Therapeutics Inc. (industry) · SION — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
144estimated
Sites
2
Country
Australia

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
DateFiledBasisWhat it is
Start2025-07-23actualWhen the study began enrolling
Primary completionJun 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJun 2026estimatedThe whole study's end, after follow-up
First posted2025-06-25actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-09-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Cystic Fibrosis (CF)

Interventions

  • Drug: SION-451
  • Drug: SION-2222
  • Drug: SION-109
  • Drug: Placebo SION-451
  • Drug: Placebo SION-2222
  • Drug: Placebo SION-109

Primary outcomes

what the primary-completion date above is the date OF
To evaluate the incidence of treatment emergent adverse events [Safety and Tolerability] of SION-451 and SION-109 when administered in combination to healthy participants
measured From Day 1 through day 21
To evaluate the incidence of treatment emergent adverse events [Safety and Tolerability] of SION-451 and SION-2222 when administered in combination to healthy participants
measured From Day 1 through day 21

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