The effect of SYX-5219 on an immune response in the skin.

2025-522217-27-00 Protocol SYX-5219-102 Human pharmacology (Phase I) - Other Ended

Start 19 Nov 2025 · End 20 Mar 2026 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol SYX-5219-102

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 20
Countries 1
Sites 1

Atopic dermatitis (AD)

Key facts

Sponsor
Sitryx Therapeutics Limited
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Diseases [C] - Skin and Connective Tissue Diseases [C17]
Trial duration
19 Nov 2025 → 20 Mar 2026
Decision date (initial)
2025-11-14
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

Atopic dermatitis (AD)

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Sitryx Therapeutics Limited

Sponsor organisation
Sitryx Therapeutics Limited
Address
101 Bellhouse Building, Magdalen Centre, The Oxford Science Park Magdalen Centre The Oxford Science Park
City
Oxford
Postcode
OX4 4GA
Country
United Kingdom

Scientific contact point

Organisation
Sitryx Therapeutics Limited
Contact name
Niamh Richmond

Public contact point

Organisation
Sitryx Therapeutics Limited
Contact name
Niamh Richmond

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Netherlands Ended 20 1
Rest of world 0

Investigational sites

Netherlands

1 site · Ended
Centre for Human Drug Research
Dermatology, Zernikedreef 8, 2333 CL, Leiden

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 2025-11-19 2026-03-20 2025-11-25 2026-01-06

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-09-15 Netherlands Acceptable
2025-11-14
2025-11-14