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Clinical Study of DA-007 for the Treatment of Chemotherapy Induced Alopecia

NCT06762548 · Status: NOT_YET_RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 140

Last updated 2025-05-23

No results posted yet for this study

Summary

Clinical Study of DA-007 As a Treatment for Chemotherapy Induced Alopecia

Conditions

  • Chemotherapy Induced Alopecia
  • Chemotherapy Side Effects

Interventions

DRUG

DA-007

Topical α1 agonist combination of Phenylephrine + Tyramine + Synephrine

DRUG

Placebo

Topical placebo solution

Sponsors & Collaborators

  • Daniel Alain, Inc.

    collaborator UNKNOWN

  • Follea International Limited

    collaborator INDUSTRY

  • Applied Biology, Inc.

    lead INDUSTRY

Principal Investigators

  • Andy Goren, MD · University of Rome G. Marconi

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-10-10
Primary Completion
2026-09-11
Completion
2026-11-06

Countries

  • Italy

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06762548 on ClinicalTrials.gov