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ADX-850

Phase 1

Hypertension | Small molecule | Cardiovascular |ADARx Pharmaceuticals, Inc.|Trials Updated: Oct 26, 2026

ADX-850 development status

Highest phase Phase 1
Registered trials 1 across 1 sponsor since Jan 2024

ADX-850 target and mechanism

ModalitySmall molecule

Also known as siRNA

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLED
Total Trials1
Total Enrollment28

FDA Designations

No designations recorded

ADX-850 clinical trials

ADX-850 · 1 trial · 2 indications

Phase 1 1
NCT06205628Safety, Tolerability, PK and PD of ADX-850 in Participants With HypertensionHypertension
ACTIVE NOT_RECRUITING28 Analytics
PHASE1ACTIVE NOT_RECRUITING
Safety, Tolerability, PK and PD of ADX-850 in Participants With Hypertension
HypertensionUnlock trial analytics

Study Endpoints

Primary Endpoints

Safety of ADX-850 in Participants with Hypertension
365 days

Incidence, relationship and severity of adverse events and serious adverse events

Secondary Endpoints

Pharmacokinetics (PK) of ADX-850 - Maximum Concentration
8 days
Pharmacokinetics (PK) of ADX-850 - Time to Maximum Concentration
8 days
Pharmacokinetics (PK) of ADX-850 - Exposure
8 days
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Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelSEQUENTIAL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
ADX-850EXPERIMENTAL -
PlaceboPLACEBO_COMPARATOR -

Interventions

NameTypeDescription
ADX-850DRUGsiRNA duplex oligonucleotide
PlaceboDRUGSaline
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Eligibility Criteria

Age Range18 Years to 65 Years
SexALL
Healthy VolunteersNo
Study Sites3

Key Inclusion Criteria: * Body mass index (BMI) between 18 and 35 kg/m2 * Mild to moderate hypertension, mean of \>130 and \<165mmHg * No use of antihypertensive medication for a minimum of 2 weeks * Willing and able to comply with all study requirements * Willing to take irbesartan as concomitant ...

Countries:Australia
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