Status:
COMPLETED
Safety and Tolerability, Pharmacokinetic and Pharmacodynamic Study With Inzomelid
Lead Sponsor:
Inflazome UK Ltd
Conditions:
Healthy
Eligibility:
All Genders
18-70 years
Phase:
PHASE1
Brief Summary
This is a first in human (FIH), single-centre, double blind, randomised, cross-over, SAD followed by a MAD study of Inzomelid. The study is designed to evaluate the safety, tolerability, PK, PD, and f...
Eligibility Criteria
Inclusion
- Inclusion Criteria- Healthy Volunteers:
- Healthy male or female volunteers, aged 18 to 65 years (inclusive at the time of informed consent);
- Participants must be in good general health, with no significant medical history, have no clinically significant abnormalities on physical examination at Screening and/or before administration of the initial dose of study drug;
- Participants must have a Body Mass Index (BMI) between ≥18.0 and ≤32.0 kg/m2 at Screening;
- Inclusion Criteria- CAPS Patients:
- \* Patients with a confirmed diagnosis of CAPS (FCAS, NOMID, or MWS) aged 18 to 70 years (inclusive at the time of informed consent);
- Exclusion Criteria- Healthy Volunteers:
- Pregnant or lactating at Screening or planning to become pregnant (self or partner) at any time during the study, including the follow-up period;
- Prior or ongoing medical conditions, medical history, physical findings, or laboratory abnormality that, in the Investigator's (or delegate's) opinion, could adversely affect the safety of the participant;
- Presence of any underlying physical or psychological medical condition that, in the opinion of the Investigator, would make it unlikely that the participant will comply with the protocol or complete the study per protocol;
- Exclusion Criteria- CAPS Patients:
- Live vaccinations within 3 months prior to Screening, for the duration of the study and for up to 3 months following the last dose of study drug;
- Positive QuantiFERON test at the Screening visit or within 2 months prior to Screening.
- Participants who have a positive QuantiFERON test with documentation of BCG vaccination, who are at low environmental risk for TB infection or reactivation, and have a negative chest X-ray can be included;
- \* Pregnant or lactating at Screening or planning to becomepregnant (self or partner) at any time during the study, including the follow-up period;
Exclusion
Key Trial Info
Start Date :
July 16 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 23 2020
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT04015076
Start Date
July 16 2019
End Date
March 23 2020
Last Update
March 27 2020
Active Locations (1)
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1
Nucleus Network
Melbourne, Queensland, Australia