Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07077395

Finding Links Between Hot flASHes and CardioVascular Disease

The goal of this clinical trial is to learn if neurokinin-1/neurokinin-3 receptor antagonist elinzanetant improves blood vessel health in women with moderate to severe hot flashes. The main questions it aims to answer is does neurokinin-1/neurokinin-3 receptor antagonist elinzanetant improve blood vessel health?

Recruiting

Interested in participating?

Request Info

Key information

Age range

40 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Brigham and Women's Hospital, Boston, Massachusetts, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 40-65 years
  • Peri- and post-menopausal women (STRAW -1 to +1)
  • Moderate or high vasmotor symptom burden
  • Cardiometabolic disease (as evidenced by ≥ 2 of the following):
  • Obesity (body mass index ≥ 30 kg/m2)
  • Elevated waist circumference (≥ 88 cm)
  • Elevated triglycerides (≥ 150 mg/dL or drug treatment)
  • Reduced HDL-cholesterol (<50 mg/dL or drug treatment)
  • Elevated blood pressure (≥ 130 mmHg systolic blood pressure or ≥ 85 mmHg diastolic blood pressure, or drug treatment)
  • Elevated fasting glucose (≥ 100 mg/dL or drug treatment)

Exclusion criteria

  • Inability to provide informed consent or comply with study protocol
  • Major comorbidities: cancer, end-stage renal (eGFR <45 mL/min/1.73 m2), liver or lung disease
  • Concomitant use of strong or moderate cytochrome P450 3A4 inhibitors
  • Elevated liver function tests (ALT, AST, and/or total bilirubin ≥2x ULN)
  • Undiagnosed uterine bleeding over past 6 months

Treatment and study plan

elinzanetant - reference formulation

Drug

elinzanetant 120 mg daily x 12 weeks

Placebo

Drug

placebo daily x 12 weeks

Primary outcomes

  1. brachial artery flow mediated dilation

    Time frame: 12 weeks

Secondary outcomes

  1. concentration of inflammatory protein biomarkers

    Time frame: 12 weeks

    • General inflammatory markers: hsCRP, IL-8, TNF-ɑ/β
    • Leukocyte adhesion markers: MCP-1, ICAM-1
    • Markers of vascular homeostasis: ANGPT1, VEGFA, HB-EGF

Study contacts

Contact information is provided by the study sponsor or research team.

Kamila Bielawski

CONTACT

[email protected]

617-724-3064

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Registry information

Acronym: FLASH-CV:

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Jul 22, 2025
Registry last updated
May 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.