Clinical trial • Phase II • Endocrinology

cagrilintide for Obesity

Phase II trial of cagrilintide for Obesity. None/Not specified-controlled. 234 participants.

Overview

Trial Therapeutic Area
Endocrinology
Trial Disease
Obesity
Trial Stage
Phase II
Drug Modality
Peptide/protein/enzyme

Key dates

Initial CTIS Submission Date
12-02-2026
First CTIS Authorization Date
21-04-2026

Trial design

None/Not specified-controlled Phase II trial across 1 site in Germany.

Comparator
None/Not specified
Target Sample Size
234

Eligibility

Recruits 234 Vulnerable population selected: true; no further details on consent or assent handling are provided in the available record..

Vulnerable Population
Vulnerable population selected: true; no further details on consent or assent handling are provided in the available record.

Recruitment

Planned Sample Size
234
Recruitment Window Months
13

Geography

Total Number Of Sites
1
Total Number Of Participants
234

Germany

Earliest CTIS Part Ii Submission Date
09-04-2026
Latest Decision Or Authorization Date
21-04-2026
Processing Time Days
12
Number Of Sites
1
Number Of Participants
234

Sites

Site Name
Klinikum Westend Haus 31, Spandauer Damm 130, Charlottenburg
Department Name
101; Parexel Early Phase Unit Berlin
Contact Person Name
Bartlomiej Kozak
Contact Person Email
bartlomiej.kozak@parexel.com

Sponsor

Primary sponsor

Full Name
Novo Nordisk A/S
Organisation Type
Pharmaceutical company
Country Of Registered Address
Denmark

Contract research organisations

Name
PAREXEL International GmbH

Investigational products

Investigational Product Name
cagrilintide
Active Substance
cagrilintide
Modality
Peptide/protein/enzyme

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