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A Study to See How Safe a New Medicine (NNC0642-1895) is in Healthy People
A First in Human Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Intravenous Administrations of NNC0642-1895 in Healthy Adults
Who can join
Ages 18 to 55 · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Male or female (sex assigned at birth, inclusive of all gender identities). * Age 18-55 years (both inclusive) at the time of signing the informed consent. * Body Mass Index (BMI) between 18.5 to 29.9 kilogram per square meter (kg/m\^2) (both inclusive) at screening * 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, as judged by the investigator. Exclusion Criteria: * Known or suspected hypersensitivity to study intervention(s) or related products. * Any laboratory safety parameters at screening outside the below laboratory ranges, see designated reference range documents for specific values: * Alanine aminotransferase (ALT) greater than (\>) Upper limit of normal (ULN) +10 percent (%) * Aspartate aminotransferase (AST) \> ULN +20% * Bilirubin \> ULN +20% * Creatinine \> ULN +10% * Absolute neutrophil count \> ULN * Absolute neutrophil count less than (\<) Lower limit of normal (LLN) * Platelet count \> ULN * Platelet count \< LLN * Supine blood pressure at screening outside the range of 90-139 millimeters of mercury (mmHg) for systolic or 50-89 mmHg for diastolic * Heart rate outside the range of 50-90 beats/min at screening * Use of prescription (except contraceptives) or non-prescription medicinal products within 14 days before screening. Occasional use of over-the-counter acetaminophen or Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) at their labelled doses is permitted.
About the study
This study is testing a new medicine, in healthy adults to assess its safety and understand how it behaves in the body. The purpose of this study is to evaluate the safety, tolerability, and how the body responds to a single dose of NNC0642-1895 in healthy adults. Participant will either get study medicine (NNC0642-1895) or placebo (a treatment that has no active medicine in it). Which treatment a participant receives is decided by chance. NNC0642-1895 is a new medicine that is being tested in humans for the first time and is not currently available for doctors to prescribe. The study will last for about 94 days (approximately 14 weeks).
What is being tested
- NNC0642-1895 (drug)
- Placebo (drug)
Sponsor: Novo Nordisk A/S · Participants: 148 · Started: Sep 17, 2026
Contact the study team
- Novo Nordisk · Phone: (+1) 866-867-7178
Official record on ClinicalTrials.gov — NCT07829406
Locations in the U.S.
| Utah | ICON-Salt Lake City, Salt Lake City |
From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.