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RecruitingNCT07077395FLASH-CV:Updated May 20, 2026

Finding Links Between Hot flASHes and CardioVascular Disease

A Phase 2 interventional study of elinzanetant - reference formulation and placebo in Menopause-related Hot Flashes, sponsored by Massachusetts General Hospital. Recruiting at 2 sites in United States. Open to female participants aged 40 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-05-20.

Sponsored by Massachusetts General Hospital · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Mar 2026; still recruiting 8 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
40 Years to 65 Years
Sex
Female
01

Study summary

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?

02

Conditions studied

  • Menopause-related Hot Flashes

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Keywords

  • menopause
  • hot flashes
  • heart health
03

In context

Hot Flashes

339 studies on the registry are indexed under Hot Flashes; 56 are open to participants now.

This study's planned enrollment of 80 is below the median of 90 across 306 interventional studies indexed under Hot Flashes.

Browse Hot Flashes studies →

Lead sponsor

Massachusetts General Hospital is the lead sponsor of 2,586 studies on the registry; 447 are open to participants now.

Of its 222 completed or terminated interventional studies of FDA-regulated products, 168 (76%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 65 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 40-65 years
  • Peri- and women (STRAW -1 to +1)
  • Moderate or high vasmotor symptom burden
  • Cardiometabolic disease (as evidenced by ≥ 2 of the following):

    • Obesity ( ≥ 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

Exclusion Criteria:

  • Inability to provide or comply with study protocol
  • Major comorbidities: cancer, end-stage renal ( \<45 mL/min/1.73 m2), liver or lung disease
  • Concomitant use of strong or moderate cytochrome P450 3A4 inhibitors
  • Elevated liver function tests (, AST, and/or total ≥2x )
  • Undiagnosed uterine bleeding over past 6 months
Terms in these criteria, in plain language(7)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
80 participants (estimated)

Study arms

  • Active comparator
    elinzanetant 120 mg daily for 12 weeks

    Drug: elinzanetant - reference formulation

  • Placebo comparator
    Placebo daily for 12 weeks

    Drug: placebo

Interventions

  • Drugelinzanetant - reference formulation

    elinzanetant 120 mg daily x 12 weeks

  • Drugplacebo

    placebo daily x 12 weeks

06

What researchers measure

Primary outcomes

  1. brachial artery flow mediated dilation

    Time frame: 12 weeks

Secondary outcomes

  1. concentration of inflammatory protein biomarkers

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

    Time frame: 12 weeks

07

Study locations

2 of 2 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Mar 2026 (actual). Primary completion is estimated for Jun 2029, 39 months after the start.

Of 24 phase 2 interventional studies under Hot Flashes, half reached primary completion within 14 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 54. This study's planned 39 months is above that.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 11, 2025
First posted
Jul 22, 2025
StartActual
Mar 1, 2026
Primary completionEst.
Jun 2029
CompletionEst.
Sep 2029
Last update
May 20, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07077395
Responsible party
Emily Lau (Principal Investigator, Massachusetts General Hospital) — Principal investigator
First posted
Jul 22, 2025
Start date
Mar 1, 2026
Primary completion
Jun 2029 (estimated)
Completion
Sep 2029 (estimated)
Last update
May 20, 2026

Study contacts

Kamila Bielawski
Contact
mghflashcv@mgb.org
617-724-3064
Emily Lau, MD, MPH
principal investigator · Massachusetts General Hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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