A Study to Learn About the Study Medicine Called PF-07328948 in Adults With Heart Failure (BRANCH-HF)
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Sponsored by Pfizer (industry) · PFE — their whole pipeline →.
Phase
Phase 2
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
620estimated
Sites
142
Countries
Brazil, Bulgaria, Canada +10
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 | 2025-06-19 | actual | When the study began enrolling |
| Primary completion | 2027-11-16 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-12-14 | estimated | The whole study's end, after follow-up |
| First posted | 2025-05-27 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-05-27 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Heart Failure
Interventions
- Drug: Placebo
- Drug: Low Dose PF-07328948 — also filed as low dose
- Drug: Medium Dose PF-07328948 — also filed as medium dose
- Drug: High Dose PF-07328948 — also filed as High dose
Primary outcomes
what the primary-completion date above is the date OFNumber of Participants with Clinical Events
measured over 36 weeks
Change From Baseline in 6-Minute Walk Test (6MWD)
measured Baseline, week 36 post-dose
Change From Baseline in Kansas City Cardiomyopathy Questionnaire Overall Total Symptom Score (KCCQ-23 TSS)
measured Baseline, week 36
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