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OpenTrials
Active, Not Recruiting

NCT Number: NCT06205628

Safety, Tolerability, PK and PD of ADX-850 in Participants With Hypertension

This Phase 1 study will evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of ADX-850 in participants with hypertension.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

CMAX Clinical Research, Adelaide, South Australia, Australia

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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 ARB therapy (Part 2 only)
  • Must be a non-smoker for the duration of the study

Key Exclusion Criteria:

  • Secondary hypertension
  • Active malignancy and/or history of malignancy in the past 5 years
  • History of liver disease, Gilbert's syndrome, nonalcoholic steatohepatitis, severe steatosis, or abnormal liver function test results
  • Any active infection or acute illness
  • Major surgery or significant traumatic injury occurring within 3 months
  • Mean sitting diastolic BP (DBP) ≥110 mmHg
  • Orthostatic hypotension
  • Significant kidney disease or eGFR <60 mL/min/1.73m2
  • Abnormal potassium levels
  • History or presence of clinically significant ECG abnormalities
  • Treatment with another investigational product within 30 days prior to the first study drug administration
  • Pregnant, intend to become pregnant during the course of the study, or lactating
  • History of alcohol abuse
  • Night shift workers (regular working hours between 10:00 PM and 6:00 AM)
  • Any other significant medical history, such as major cardiovascular events or cancer
  • Known history of intolerance to ARB medication (Part 2 only)

Treatment and study plan

ADX-850

Drug

siRNA duplex oligonucleotide

Other names: siRNA

Placebo

Drug

Saline

Primary outcomes

  1. Safety of ADX-850 in Participants with Hypertension

    Time frame: 365 days

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

Secondary outcomes

  1. Pharmacokinetics (PK) of ADX-850 - Maximum Concentration

    Time frame: 8 days

    Cmax

  2. Pharmacokinetics (PK) of ADX-850 - Time to Maximum Concentration

    Time frame: 8 days

    Tmax

  3. Pharmacokinetics (PK) of ADX-850 - Exposure

    Time frame: 8 days

    Area under the Curve (AUC)

  4. Pharmacodynamics (PD) of ADX-850 - Blood Pressure

    Time frame: 365 days

    Change from baseline in blood pressure

Sponsors and collaborators

Lead sponsor

ADARx Pharmaceuticals, Inc.

Industry

Collaborators

  • ADARx Australia Pty Ltd

Registry information

Official study title

A Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ADX-850 in Participants With Hypertension

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Jan 16, 2024
Registry last updated
Jul 27, 2026

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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