NCT05408572

Study of SON-1010 (IL12-FHAB) in Healthy Adults

A Phase 1, Randomized, Adaptive-Design, Dose-Escalation Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of SON-1010 (IL12-FHAB) in Healthy Adults
Sonnet BioTherapeutics·Phase 1·ClinicalTrials.gov·biologicalRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Healthy Adult
Drug/Device/Intervention
SON-1010 (IL12-FHAB)
Study type
Interventional
Intervention type
biological
Sponsor & location
Primary sponsor
Sonnet BioTherapeutics
Location
Melbourne, Australia
Timeline & enrollment
Phase
Phase 1
Start date
Jul 27, 2022
End date
Dec 30, 2022
Enrollment
40 participants
Primary outcome

To evaluate the safety and tolerability of SON-1010 as a single-ascending dose (SAD) in healthy adults.

Summary

SB102 is a randomized, double-blind, single center, placebo-controlled study in healthy
 adults starting with sentinel participants at each dose level to carefully assess the safety,
 tolerability, PK, and PD of SON-1010.

ICD-10 classifications
Healthy person accompanying sick personObesity, unspecifiedLifestyle-related conditionAdult-onset Still diseaseObesity
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05408572
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05408572 through Pure Global AI's free database. This Phase 1 trial is sponsored by Sonnet BioTherapeutics and is currently Recruiting. The study focuses on Healthy Adult. Target enrollment is 40 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.