A 3-part Study of SYX-5219 in Healthy Volunteers and Participants With Atopic Dermatitis

Recruiting Phase 1 Interventional Study
Moderate to Severe Atopic Dermatitis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 – 65
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
149 (estimated)
Sponsor
Sitryx Therapeutics Ltd · Industry
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About This Trial
The purpose of this study is to evaluate the study drug, SYX-5219, in a multi-part First-in-Human (FiH) study to be conducted in healthy volunteers and participants with Atopic Dermatitis (AD). The objectives of this study are to determine the safety, tolerability and levels of SYX-5219 in the blood and urine when SYX-5219 is given in each part of the study (SAD, MAD, Food Effect and Participants …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: Parts 1 \& 2 * Healthy male and female participant, between ≥ 18 to ≤ 65 years of age, inclusive, with a BMI of body mass index (BMI) of 18-32 kg/m2. * Female participant of non-childbearing potential or female of childbearing potential that is sexually abstinent. * No clinical…
Contacts

Sitryx Therapeutics

+44 (0)1865 648401

info@sitryx.com

CONTACT

Sitryx Therapeutics

+44 (0) 1865 648401

info@sitryx.com

CONTACT