Single-dose Pharmacokinetics of Pociredir in Participants With Sickle Cell Disease

Part of paid clinical trials in Miami, Florida.

Sponsor
Fulcrum Therapeutics
Study ID
NCT07431398
Phase
PHASE1
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • Pociredir — DRUG
    Pociredir tablet formulation

Study Details

This clinical trial is a study to evaluate the pharmacokinetics of the tablet formulation Pociredir in fasted and fed state participants with Sickle Cell Disease (SCD).

Key Dates

Start date
Dec 13, 2025
Status verified
Mar 2026
Primary completion
May 31, 2026
Completion
Jun 30, 2026

Study Design

Enrollment
24 participants (estimated)
Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT

Arms

  • Experimental: Fasted Cohort
    Pociredir single dose tablet formulation under fasted conditions.
  • Experimental: Fed Cohort
    Pociredir single dose tablet formulation under fed conditions (after a high-fat breakfast).

Primary Outcome Measure

Plasma concentration of pociredir under fasted and fed conditions [ Time Frame: Day 1 through Day 4 ]

Central Contacts

Locations (6)

FacilityCityStateZIPSite coordinators
Advanced Pharma - MiamiMiamiFlorida33147
305-220-2727
Omega Research GroupOrlandoFlorida32808
407-512-1054
Sonar Clinical ResearchRiverdaleGeorgia30274
404-779-2059
Neuro-Behavioral Clinical ResearchNorth CantonOhio44720
330-493-1118
University of Texas Health Science Center HoustonHoustonTexas77030-
Worldwide Clinical TrialsSan AntonioTexas78217
210-635-1515

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