A Study Understanding How Much CDR132L Enters the Bloodstream After Injection Under the Skin Compared to Injection Into a Vein in Healthy Participants

NCT07656454 | Recruiting Phase 1 FDA Drug

• 3 other identifiers: NN6706-8230U1111-1319-62492025-521329-34
• Study Type: interventional
• Target: 32
• Locations: 1 country
• Sites: 1

Brief Summary

This study is being done to understand how much of the medicine (CDR132L) enters the bloodstream after injection under the skin compared to injection into a vein in healthy people. This will help us find the best way to give the medicine to people living with heart failure. The study will assess what the body does to the medicine, and how safe it is.

Conditions

Healthy Volunteers; Heart Failure

Outcome Measures

Primary Outcomes (1)

• Area under the CDR132L plasma concentration-time curve (AUC 0-tz) from 0 hours to tz after a single dose, where tz is the time of last quantifiable concentration

  Measured as hours\*nanograms per milliliter (h\*ng/mL)

  From 0 to 840 hours after CDR132L administration

Secondary Outcomes (10)

• Area under the CDR132L plasma concentration-time curve from 0 hours and extrapolated to infinity after a single dose

  From 0 to 840 hours after CDR132L administration

• Maximum observed CDR132L plasma concentration after a single dose

  From 0 to 840 hours after CDR132L administration

• Time to maximum observed CDR132L plasma concentration after a single dose

  From 0 to 840 hours after CDR132L administration

• Terminal half-life for CDR132L after a single dose

  From 0 to 840 hours after CDR132L administration

• Area under the CDR132L plasma concentration-time curve from 0 hours to tz after a single dose, where tz is the time of last quantifiable concentration, divided by dose

  From 0 to 840 hours after CDR132L administration

Study Arms (4)

Sequence A

EXPERIMENTAL

Participants will be given dose 1 of CDR132L intravenously, followed by dose 1 of CDR132L administered subcutaneously.

Drug: CDR132L (i.v.); Drug: CDR132L (s.c.)

Sequence B

EXPERIMENTAL

Participants will be given dose 1 of CDR132L subcutaneously, followed by dose 1 of CDR132L administered intravenously.

Drug: CDR132L (i.v.); Drug: CDR132L (s.c.)

Sequence C

EXPERIMENTAL

Participants will be given dose 2 of CDR132L intravenously, followed by dose 2 of CDR132L administered subcutaneously.

Drug: CDR132L (i.v.); Drug: CDR132L (s.c.)

Sequence D

EXPERIMENTAL

Participants will be given dose 2 of CDR132L subcutaneously, followed by dose 2 of CDR132L administered intravenously.

Drug: CDR132L (i.v.); Drug: CDR132L (s.c.)

Interventions

CDR132L (i.v.) DRUG

CDR132L will be administered intravenously.

Sequence A; Sequence B; Sequence C; Sequence D

CDR132L (s.c.) DRUG

CDR132L will be administered subcutaneously.

Sequence A; Sequence B; Sequence C; Sequence D

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Male or female (sex at birth).
• Age 18-55 years (both inclusive) at the time of signing the informed consent.
• Body mass index 18.5-29.9 kilograms per square metre (kg/m\^2) (both inclusive) and body weight less than or equal to (≤) 120 kilograms (kg) at screening (visit 1).
• Considered to be generally healthy based on the medical history, physical examination, and the results of vital signs, electrocardiogram and clinical laboratory tests performed during the screening visit (visit 1), as judged by the investigator.

You may not qualify if:

• Any laboratory safety parameters at screening (visit 1) outside the below laboratory ranges, see laboratory manual for specific values.
• Alanine aminotransferase (ALT) greater than (\>) upper limit of normal (ULN) +10 percentage (%)
• Aspartate aminotransferase (AST) \>ULN +20%
• Bilirubin \>ULN +20%
• Creatinine \>ULN +10%
• Estimated glomerular filtration rate (eGFR) (Chronic Kidney Disease Epidemiology Collaboration \[CKD-EPI\]) less than (\<) 90 milliliters per minute/1.73square meter (mL/min/1.73m\^2)
• Urine albumin-to-creatinine ratio (UACR) greater than or equal to (≥) 30 milligrams per gram (mg/g)
• Second or third degree atrioventricular-block, prolongation of the QRS complex over 120 milliseconds (ms), or of the QT interval corrected using Fridericia's formula (QTcF) interval over 450 ms, or any other clinically significant abnormal electrocardiogram results as judged by the investigator at screening (visit 1).
• Supine blood pressure at screening (visit 1) outside the range of 90-139 millimeters of mercury (mmHg) for systolic or 50-89 mmHg for diastolic.
• Heart rate outside the range of 50-89 beats/minute at screening (visit 1).
• Presence or history (as declared by the participant or reported in the medical records) of cardiovascular disease including stable and unstable angina pectoris, myocardial infarction, transient ischaemia, stroke, heart failure, cardiac decompensation, clinically significant arrhythmia and clinically significant conduction disorders.
• Known history of severe symptomatic untreated anaemia in the 90 days prior to screening (visit 1) (e.g., haemoglobin \<90 grams per litre (g/L))
• Presence or history (as declared by the participant or reported in the medical records) of acute or chronic kidney disease or injury.
• Presence of thrombocytopenia, defined as thrombocyte count \<150 x 10\^9 cells/L at screening (visit 1), or history (as declared by the participant or reported in the medical records) of bleeding disorder.
• Presence or history (as declared by the participant or reported in the medical records) of conditions associated with disruption of blood-brain barrier (e.g. multiple sclerosis).

Sponsors & Collaborators

• Novo Nordisk A/S: lead

Study Sites (1)

Parexel International GmbH

Berlin, 14050, Germany

RECRUITING

MeSH Terms

Conditions

Heart Failure

Condition Hierarchy (Ancestors)

Heart Diseases; Cardiovascular Diseases

Study Officials

• Clinical Transparency (dept. 2834)

  Novo Nordisk A/S

  STUDY DIRECTOR

Central Study Contacts

Novo Nordisk

CONTACT

(+1) 866-867-7178; clinicaltrials@novonordisk.com

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 14, 2026
• First Posted: June 18, 2026
• Study Start: June 17, 2026
• Primary Completion (Estimated): December 31, 2026
• Study Completion (Estimated): December 31, 2026
• Last Updated: June 30, 2026

Record last verified: 2026-06

Data Sharing

• IPD Sharing: Will share

Locations

DE (1)