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Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Pociredir

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NCT05169580

Sponsored by Fulcrum Therapeutics (industry) · FULC — their whole pipeline →.

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Na · None · Treatment
Enrollment
45actual
Sites
18
Countries
Nigeria, South Africa, 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
DateFiledBasisWhat it is
Start2021-12-13actualWhen the study began enrolling
Primary completion2026-01-20actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-01-20actualThe whole study's end, after follow-up
First posted2021-12-27actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-02-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Sickle Cell Disease
  • Sickle Cell Anemia

Intervention

  • Drug: Pociredir oral capsule(s) — also filed as FTX-6058

Primary outcomes

what the primary-completion date above is the date OF
Treatment-Emergent Adverse Events
measured Up to approximately 16 weeks of monitoring
Plasma Concentrations of Pociredir
measured Days 1, 14, 28, 42, 56, 70, 84 and 91

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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