Phase 2 Heart Disease Trial, Recruiting NCT06122779 Sponsor: Bristol-Myers Squibb Condition: Heart Disease
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Phase 2 Heart Disease Trial, Recruiting

NCT06122779
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults who have been diagnosed with stable heart failure with preserved ejection fraction (HFpEF) — a type of heart failure where the heart still pumps a normal amount of blood but does not relax properly — and who are experiencing symptoms from this condition

Who may not be able to join:

  • People who have been diagnosed with certain heart muscle conditions, such as hypertrophic cardiomyopathy (a thickening of the heart muscle) or conditions where abnormal substances build up in the heart (such as cardiac amyloidosis)
  • People who have any other serious or active health condition that could affect study results or put them at risk during the trial
  • There are additional criteria not listed here that the trial site will assess (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 15 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Bristol-Myers Squibb, Bristol-Myers Squibb

Phone: 855-907-3286

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
7 November 2023
Est. completion
14 December 2026

Where this trial is recruiting

🇦🇷 Argentina 🇨🇦 Canada 🇨🇳 China 🇮🇱 Israel 🇮🇹 Italy 🇯🇵 Japan 🇵🇱 Poland 🇰🇷 South Korea 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Incidence of treatment emergent adverse events (TEAEs); Incidence of serious adverse events (SAEs); Incidence of AEs leading to treatment discontinuation

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov