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A Study to Evaluate BMS-986470 in Healthy Volunteers and Participants With Sickle Cell Disease

Recruiting · Phase 1, Phase 2 · NCT06481306

Conditions: Anemia, Sickle Cell, Healthy Volunteers

At a glance

Research payments reported, 2025
$25,050
U.S. investigators named
5
Sites paid
6
Planned or actual enrollment
224

About the trial

Sponsor
Bristol-Myers Squibb
Tested
BMS-986470 (drug), Placebo (drug), Famotidine (drug), Pantoprazole (drug)
Dates
Started 2024-07-17; completion 2027-11-16
Results posted
Not yet

The purpose of this study is to evaluate the safety and tolerability, pharmacokinetics and pharmacodynamics, pH and food effect, and preliminary efficacy of BMS-986470 in healthy volunteers and participants with sickle cell disease.

From ClinicalTrials.gov, last updated 2026-08-18. Full record, eligibility and contacts (opens in a new tab)

Industry funding

E.r. Squibb & Sons, L.l.c. reported $25,050 in research payments for this study in 2025 (6 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.