A Randomized Study in Healthy Participants to Identify the Optimal Subcutaneous Injection Strategy for COR-1167

2026-526096-31-00 Protocol COR1167-102 Human pharmacology (Phase I) - Other Authorised, recruitment pending

Status Authorised, recruitment pending · 1 EU/EEA countries · 1 sites · Protocol COR1167-102

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Authorised, recruitment pending
Participants planned 20
Countries 1
Sites 1

Chronic Heart Failure

Key facts

Sponsor
Corteria Pharmaceuticals
Participant type
Healthy volunteers
Age range
18-64 years, 65+ years
Gender
Male and Female
Therapeutic area
Diseases [C] - Cardiovascular Diseases [C14]
Decision date (initial)
2026-05-13
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Chronic Heart Failure

VersionLevelCodeTermSystem organ class
20.0 LLT 10008908 Chronic heart failure 10007541

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Corteria Pharmaceuticals

Sponsor organisation
Corteria Pharmaceuticals
Address
128 Rue La Boetie
City
Paris
Postcode
75008
Country
France

Scientific contact point

Organisation
Corteria Pharmaceuticals
Contact name
Chief Medical Officer - Francesca Lawson

Public contact point

Organisation
Corteria Pharmaceuticals
Contact name
Chief Medical Officer - Francesca Lawson

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Netherlands Authorised, recruitment pending 20 1
Rest of world 0

Investigational sites

Netherlands

1 site · Authorised, recruitment pending
Pharmaceutical Research Associates Group B.V.
Program Management, Van Swietenlaan 6, 9728 NZ, Groningen

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2026-03-27 Netherlands Acceptable
2026-05-13
2026-05-13