150 mg CIT-013 phase 1 trial

2026-526153-34-00 Protocol CITRYLL006 - Citysky Human pharmacology (Phase I) - Other Authorised, recruiting

Start 26 May 2026 · Status Authorised, recruiting · 1 EU/EEA countries · 1 sites · Protocol CITRYLL006 - Citysky

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Authorised, recruiting
Participants planned 10
Countries 1
Sites 1

Immune mediated inflammatory diseases

Key facts

Sponsor
Citryll B.V.
Participant type
Healthy volunteers
Age range
18-64 years, 65+ years
Gender
Male and Female
Therapeutic area
Diseases [C] - Immune System Diseases [C20]
Trial duration
26 May 2026 → ongoing
Decision date (initial)
2026-05-22
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

External identifiers

EU CT number
2026-526153-34-00
ClinicalTrials.gov
NCT07499908

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Immune mediated inflammatory diseases

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Citryll B.V.

Sponsor organisation
Citryll B.V.
Address
Rk Gebouw, Kloosterstraat 9 Kloosterstraat 9
City
Oss
Postcode
5349 AB
Country
Netherlands

Scientific contact point

Organisation
Citryll B.V.
Contact name
Maarten Kraan

Public contact point

Organisation
Citryll B.V.
Contact name
Nicole Keijzer

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Netherlands Authorised, recruiting 10 1
Rest of world 0

Investigational sites

Netherlands

1 site · Authorised, recruiting
Pharmaceutical Research Associates Group B.V.
N/A, Van Swietenlaan 6, 9728 NZ, Groningen

Country notifications

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

Country Trial startTrial end Recruitment startRecruitment end Early termination
Netherlands 2026-05-26

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2026-04-03 Netherlands Acceptable
2026-05-22
2026-05-22