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Heart FailureEarly Phase 1NCT07606183

Effects of Different Forms of a Natural Heart Hormone on Blood Pressure and Fluid Balance in Healthy Volunteers

A Early Phase 1 study of Heart Failure and Hypertension, run by Peter Fruergaard Andersen at 1 site in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The human heart produces hormones that help regulate blood pressure and fluid balance in the body. One of these hormones is atrial natriuretic peptide (ANP). ANP lowers blood pressure by relaxing blood vessels and increasing urinary excretion by the kidneys. Read more about this study

Who is it for?
Ages 18 to 30 years, men onlyHealthy volunteers can take part
Conditions the study is for
Heart Failure, Hypertension, Kidney Failure
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
17 participants
Where
1 siteDenmark
Study dates
1 May 2022to 30 Mar 2026
Phase
Early Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 30 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Healthy male volunteers
  • Age: 18-30 years
  • BMI: 20-25 kg/m²
  • Body weight ≤90 kg (amended protocol)
  • Normal hemoglobin
  • Ability to provide informed consent

Who cannot join

  • Acute illness within two weeks
  • Chronic cardiovascular, renal, hepatic, pulmonary, metabolic or malignant disease
  • Hypotension or history of syncope
  • Smoking
  • Substance or alcohol abuse
  • Recent blood donation (<3 months)
  • Medication that cannot be safely interrupted

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • 4) Department of Clinical Pharmacology, Copenhagen University Hospital - Bispebjerg and Frederiksberg, Copenhagen, Denmark

    Copenhagen, 2400

Other trials in Denmark

About this study

Official title: Effects of Glycosylated Atrial Natriuretic Peptide on Blood Pressure and Fluid Balance in Healthy Volunteers

The human heart produces hormones that help regulate blood pressure and fluid balance in the body. One of these hormones is atrial natriuretic peptide (ANP). ANP lowers blood pressure by relaxing blood vessels and increasing urinary excretion by the kidneys.

Previous research has demonstrated that ANP naturally carries a small sugar molecule attached. This sugar moiety is produced endogenously and can modify the biological activity of ANP. When this sugar is present, ANP may affect blood vessels and renal function differently compared with the non-glycosylated form.

The present study examines how this sugar modification alters the physiological effects of ANP. This is achieved by administering ANP, either with or without the attached sugar molecule, via intravenous infusion. The study aims to determine whether glycosylated ANP differs from the native form in its effects on blood pressure and fluid balance.

Read the detailed description

Introduction Atrial natriuretic peptide (ANP) is a critical component of the natriuretic peptide family and plays a central role in cardiovascular homeostasis. ANP is primarily synthesized and secreted by atrial myocytes in response to atrial stretch and related stimuli. The peptide exerts biological effects through binding to specific receptors, leading to activation of A-type guanylyl cyclase (GC) (also known as NPR-A) and subsequent production of cyclic guanosine monophosphate (cGMP). This signaling cascade induces vasodilation, natriuresis, and diuresis, thereby contributing to regulation of blood pressure and fluid balance.

The concept of proteoforms refers to the various molecular forms that a protein can assume, arising from genetic variation, alternative splicing, and post-translational modification. ANP proteoforms therefore comprise molecular variants of ANP with potentially distinct biological activities and clinical implications.

ANP proteoforms have diagnostic and prognostic value in cardiovascular disease. Elevated ANP and related peptides indicate increased cardiac stress and are observed in conditions such as heart failure, hypertension, and acute coronary syndromes. Measurement of ANP, together with B-type natriuretic peptide (BNP) and N-terminal proBNP (NT-proBNP), is widely used in clinical practice to assist diagnosis and guide management (Volpe 2021).

Beyond diagnostic utility, ANP possesses therapeutic potential. Vasodilatory and natriuretic properties make ANP an attractive candidate for treatment of conditions associated with fluid overload and hypertension. Recombinant ANP analogues have been used clinically in acute heart failure.

Recent advances highlight strategies to enhance natriuretic peptide activity. Inhibition of neprilysin prolongs peptide half-life and biological effect. Combined neprilysin inhibition and angiotensin receptor blockade has demonstrated clinical benefit in heart failure (McMurray 2013).

Post-translational modification, including glycosylation, further diversifies ANP function. Glycosylated ANP refers to peptide forms containing covalently attached carbohydrate groups, typically linked to serine or threonine residues. This modification alters receptor binding, biological activity, and resistance to proteolytic degradation. Glycosylation may therefore influence the physiological and therapeutic profile of ANP. Recent observations suggest that glycosylation modulates interaction with natriuretic peptide receptors and downstream signaling pathways (Hansen 2019).

Objectives, Hypothesis, and Endpoints The primary objective of the study is to clarify the physiological significance of glycosylated ANP in humans.

The primary hypothesis is that glycosylated ANP regulates blood pressure without inducing diuresis.

Primary endpoints include diuresis and natriuresis during intervention. Secondary endpoints include changes in blood pressure and plasma and urinary concentrations of natriuretic peptides, renin-angiotensin-aldosterone parameters, electrolytes, cyclic nucleotides, metabolic substrates, stress hormones, and amino acids.

Methods and Study Design The study is designed as a randomized, double-blind, placebo-controlled crossover investigation. Each participant acts as an individual control. Randomization assigns infusion with ANP, glycosylated ANP (gANP), or saline on separate study days.

Following written informed consent, screening is performed after overnight fasting and includes clinical assessment, laboratory evaluation, and urine testing.

On study days, participants are admitted after a 10-hour fast. Procedures include bladder emptying, venous catheter placement, baseline sampling, and continuous blood pressure monitoring. Infusions of ANP, gANP, or saline are administered according to protocol.

Blood samples are obtained at predefined intervals, and urine is collected during and after infusion. Ultrasonographic assessment of vascular parameters and bladder volumes is performed where applicable.

Study Population Inclusion criteria comprise healthy male individuals aged 18-30 years with normal body mass index and hemoglobin levels.

Exclusion criteria include recent illness, chronic disease, hypotension, smoking, substance abuse, recent blood donation, and medication use incompatible with study requirements.

Safety and Ethics Both ANP and gANP are associated with blood pressure reduction. Continuous monitoring is implemented, and infusion is discontinued if symptomatic hypotension occurs.

The study is conducted in accordance with ethical guidelines, with approval from the relevant ethics committee.

Biobank and Data Handling Biological samples are coded and stored according to regulatory requirements. Analyses are performed at designated institutions, and remaining material is handled in accordance with approved protocols.

Funding and Registration The study is supported by Innovation Fund Denmark. A patent application related to glycosylated ANP has been filed.

Trial registration was completed following recognition of registry requirements, with all study parameters finalized prior to participant enrollment and approved by the ethics committee.

Being tested
Infusion of two different cardiac peptides plus vehicle
Keywords
ANP, atrial natriuretic peptide, glycosylation, post-translational modification, peptide
Medical subject headings
Heart Failure, Hypertension, Renal Insufficiency, Atrial Fibrillation, Familial, 6

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Infusion of two different cardiac peptides plus vehicleOther

    Interventions

    Original protocol:

    ANP: 200 pmol/kg/min for 120 minutes gANP: 200 pmol/kg/min for 120 minutes

    Amended protocol:

    ANP: 200 pmol/kg/min for 60 minutes gANP: 300 pmol/kg/min for 60 minutes

    Control:

    Saline infusion at 0.7 mL/kg/hour

Study groups in NCT07606183
Study groupRoleWhat they receive
Atrial Natriuretic Peptide (ANP) - a well described cardiac hormoneActive comparatorAtrial Natriuretic Peptide (ANP) Participants receive an intravenous infusion of native atrial natriuretic peptide (ANP), a naturally occurring heart hormone known to lower blood pressure by relaxing blood vessels and increasing salt and water excretion by the kidneys. ANP is administered at a fixed weight-adjusted dose over a defined infusion period, followed by post-infusion observation and monitoring of blood pressure, urine output, and blood markers.
Receives: Other: Infusion of two different cardiac peptides plus vehicle
Glycosylated Atrial Natriuretic Peptide (gANP) - a naturally occurring modified cardiac hormoneExperimentalParticipants receive an intravenous infusion of glycosylated atrial natriuretic peptide (gANP), a naturally occurring sugar-modified form of ANP. Glycosylation alters the stability and biological activity of the hormone. gANP is administered at a weight-adjusted dose comparable to or slightly higher than native ANP, according to protocol amendments, with the same monitoring procedures. The purpose is to assess whether the sugar-modified form produces different effects on blood pressure, fluid balance, and vascular function compared with native ANP.
Receives: Other: Infusion of two different cardiac peptides plus vehicle
Placebo (Saline)Placebo comparatorParticipants receive an intravenous infusion of isotonic saline at a low, weight-adjusted rate. This arm serves as a placebo control to account for the effects of the infusion procedure, time, and study conditions. The volume administered is equal to both of the active days. All measurements and observations are identical to those performed during the active intervention arms.
Receives: Other: Infusion of two different cardiac peptides plus vehicle

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Diuresis and natriuresis

    Primary Objective Diuresis and natriuresis are quantified immediately after conclusion of peptide/placebo administration and repeated after an additional two hours of observation.

    Measured: Collection and quantification will take place after completion of two hours of peptide/placebo administration and again after two hours of observation

Secondary outcomes (3)
  1. Blood pressure

    Blood pressure will be measured during infusion and observation on all experimental days.

    Measured: Measurement will take place every ten minutes throughout the experimental day.

  2. Metabolic markers

    Metabolic markers in plasma will be quantified (listed in detailed description) in plasma

    Measured: During and after infusion of peptide/placebo with 20-30 min interval.

  3. cyclic GMP

    Concentration of the second messenger, cGMP, in plasma and urine.

    Measured: Quantification will take place once every hour (plasma) and every two hours (urine)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 May 2026
  2. Study start1 May 2022
  3. Primary completion30 Mar 2023
  4. Study completion30 Mar 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Early Phase 1
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Model description
This randomized, double blinded, placebo controlled, crossover study investigates the physiological effects of intravenous glycosylated ANP compared with naked ANP and saline in healthy male volunteers, with particular focus on blood pressure regulation, diuresis, natriuresis, and vascular function.
Masking
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
17 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07606183
Sponsor's protocol ID
77354/H-21000305
Status last verified
May 2026
First submitted
28 Apr 2026
Last updated
26 May 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Early Phase 1 study of Heart Failure and Hypertension, run by Peter Fruergaard Andersen at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Diuresis and natriuresis (time frame: Collection and quantification will take place after completion of two hours of peptide/placebo administration and again after two hours of observation). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 May 2026.

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