Clinical Trials in Italy / NCT07033845
Recruiting
Early Phase 1
Pharmacokinetic Study of Topical Phenylephrine
NCT07033845 · tracked via the Priya Life Science Italy tracker
Condition(s) studied
Chemotherapy Induced AlopeciaChemotherapy Side Effects
Investigational drug(s) / intervention(s)
Phenylephrine
Phenylephrine: Topical Phenylephrine
Study summary
Pharmacokinetic Study of Topical Phenylephrine
Eligibility
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)
- Pharmacokinetic profile of phenylephrine — Week [0,3]
Determine the amount of phenylephrine and its metabolites in serum daily scalp application of topical phenylephrine for a period of 3 weeks
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| University of Rome ("G. Marconi") | Rome | Italy | Recruiting |
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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 NCT07033845 on ClinicalTrials.gov ↗ ← All trials in Italy