Clinical Study of DA-020 for the Treatment of Chemotherapy Induced Alopecia

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexFemale
Age18-65
SponsorApplied Biology, Inc.

About this trial

Clinical Study of DA-020 as a Treatment for Chemotherapy Induced Alopecia

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosed with stage I or stage II breast cancer

Scheduled but not begun, at least 4 cycles of taxane and/or anthracycline-based chemotherapy.

Ages 18-65

Able to give informed consent

Disqualifiers

Resting blood pressure outside the range of 105-140/ 55-99

Uncontrolled or severe hypertension

Female pattern hair loss or hair loss disorder

Folliculitis

Trial design

Design model

Parallel

Treatments tested in this trial

  • DA-020

    Drug

    7mL application of DA-020 (Topical Oxymetazoline)

  • Placebo

    Drug

    Topical placebo solution

  • DA-020 and Hyperforin

    Drug

    7mL application of DA-020 (Topical Oxymetazoline) and Hyperforin (1.5%)

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: DA-020Active comparator 1 intervention
Group B: PlaceboPlacebo comparator 1 intervention
Group C: DA-020 and Hyperforin (1.5%)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Prevention of Hair Loss (Common Terminology Criteria for Adverse Events V5.0)

Amount of hair loss during chemotherapy treatment measured by the Common Terminology Criteria for Adverse Events (CTCAE) V5.0. The Common Terminology Criteria for Adverse Events is a common terminology developed by the National Cancer Institute to describe and grade adverse events related to cancer therapy.

Time frame
Week [0,12]

Secondary outcomes

1

Hair Re-Growth Post Treatment (Common Terminology Criteria for Adverse Events V5.0)

Amount of hair re-growth post chemotherapy treatment measured by the Common Terminology Criteria for Adverse Events (CTCAE) V5.0. The Common Terminology Criteria for Adverse Events is a common terminology developed by the National Cancer Institute to describe and grade adverse events related to cancer therapy.

Time frame
Week [12, 24]

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Applied Biology, Inc.

Lead sponsor

Daniel Alain, Inc.

Collaborator

Follea International Limited

Collaborator