A research study to compare blood levels of cagrilintide after multiple doses of different versions of cagrilintide in adults with overweight or obesity

2025-521384-12-00 Protocol NN9833-8285 Human pharmacology (Phase I) - Bioequivalence study Ongoing, recruiting

Start 27 Apr 2026 · Status Ongoing, recruiting · 1 EU/EEA countries · 1 sites · Protocol NN9833-8285

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Bioequivalence study
Status Ongoing, recruiting
Participants planned 234
Countries 1
Sites 1

obesity

Key facts

Sponsor
Novo Nordisk A/S
Participant type
Patients
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Diseases [C] - Nutritional and Metabolic Diseases [C18]
Trial duration
27 Apr 2026 → ongoing
Decision date (initial)
2026-04-21
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
Yes

External identifiers

EU CT number
2025-521384-12-00
WHO UTN
U1111-1314-9337

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

obesity

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Novo Nordisk A/S

Sponsor organisation
Novo Nordisk A/S
Address
Novo Alle 1
City
Bagsvaerd
Postcode
2880
Country
Denmark

Scientific contact point

Organisation
Novo Nordisk A/S
Contact name
Eu submission Hub

Public contact point

Organisation
Novo Nordisk A/S
Contact name
Eu submission Hub

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Germany Ongoing, recruiting 234 1
Rest of world 0

Investigational sites

Germany

1 site · Ongoing, recruiting
PAREXEL International GmbH
101; Parexel Early Phase Unit Berlin, Klinikum Westend Haus 31, Spandauer Damm 130, Berlin

Country notifications

Trial-start, recruitment-start, end and early-termination notifications submitted per Member State

Country Trial startTrial end Recruitment startRecruitment end Early termination
Germany 2026-04-27 2026-05-18

Application history

2 submissions — initial application plus substantial / non-substantial modifications

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2026-02-12 Germany Acceptable
2026-04-14
2026-04-21
2 SUBSTANTIAL MODIFICATION SM-1 2026-04-24 Germany Acceptable
2026-04-30
2026-06-02