ADX-850
DrugsiRNA duplex oligonucleotide
Other names: siRNA
NCT Number: NCT06205628
This Phase 1 study will evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of ADX-850 in participants with hypertension.
This study is active but is not currently recruiting participants.
18 year–65 year
All sexes
Interventional
Phase 1
CMAX Clinical Research, Adelaide, South Australia, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
siRNA duplex oligonucleotide
Other names: siRNA
Saline
Time frame: 365 days
Incidence, relationship and severity of adverse events and serious adverse events
Time frame: 8 days
Cmax
Time frame: 8 days
Tmax
Time frame: 8 days
Area under the Curve (AUC)
Time frame: 365 days
Change from baseline in blood pressure
ADARx Pharmaceuticals, Inc.
Industry
A Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ADX-850 in Participants With Hypertension
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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