Ireland
--:--IST
Starting soon Early Phase 1

Pharmacokinetic Study of DA-020

NCT07402330 · tracked via the Priya Life Science Italy tracker
Phase
Early Phase 1
Started
2026-04-16
Last updated
2026-04-13

Condition(s) studied

Chemotherapy Induced AlopeciaChemotherapy Side Effects

Investigational drug(s) / intervention(s)

DA-020 (0.1%) →DA-020 (0.2%) →DA-020 (0.5%) →

DA-020 (0.1%): DA-020 (0.1%)

DA-020 (0.2%): DA-020 (0.2%)

DA-020 (0.5%): DA-020 (0.5%)

Study summary

Pharmacokinetic Study of DA-020

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
55 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy females, age 18-55 * BMI: 18-30 kg/m² * Fitzpatrick Skin Types I-IV (to standardize absorption risk) * Scalp free from irritation, dermatologic disease, or damage * Able to refrain from using other topical scalp products Exclusion Criteria: * History of cardiovascular disease, hypertension, or arrhythmia * Scalp infections, wounds, or significant hair loss * Recent use of medications that interfere with CYP enzymes or adrenergic systems * Known sensitivity to phenylephrine or ethanol * Positive drug screen or abnormal ECG at screening

Primary outcome measure(s)

  • Concentration of DA-020 in Serum — Hours [0, 1, 2, 4, 8, 12, 24]
    Determine the amount of Oxymetazoline in serum after 1 time scalp application

Trial sites (2)

FacilityCityRegionStatus
Hospital Samel Manaus Brazil
University of Rome ("G. Marconi") Rome Italy
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07402330 on ClinicalTrials.gov ↗ ← All trials in Italy