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Active clinical trials for "Alopecia"

Results 261-270 of 449

A Study to Evaluate the Efficacy and Safety of AD-208

Androgenetic Alopecia

The purpose of this study is to evaluate the efficacy and safety of AD-208.

Completed5 enrollment criteria

Keratinocyte Growth Factor- Hair Serum for the Prevention of Chemotherapy Induced Alopecia

AlopeciaChemotherapy-Induced Change2 more

Primary aim is to provide a preliminary assessment of the efficacy of the investigational topical formula, KGF-HS, as a prophylactic treatment for chemotherapy induced alopecia. Hypothesis: KGF-HS will result in less than 50% hair loss by the end of 4 cycles of chemotherapy. The investigators will evaluate hair loss using the CTCAE (Common Terminology Criteria for Adverse Events) v4.0 alopecia grading scale.

Completed12 enrollment criteria

A Study of TDM-105795 in Male Subjects With Androgenetic Alopecia (AGA)

AlopeciaAndrogenetic

Multi-center, randomized, double-blind, vehicle-controlled, parallel group, multi-dose escalation study of TDM-105795 in male subjects, 18 to 55 years old, with Androgenetic Alopecia (AGA).

Completed30 enrollment criteria

A Phase II Study in Patients With Alopecia Areata

Alopecia Areata

This is a global Phase 2 study to evaluate the safety and effectiveness of an investigational study drug (called SHR0302) in adults with moderate to severe alopecia areata.

Completed5 enrollment criteria

New Treatment of Alopecia Areata

Alopecia Areata

Abstract: Alopecia areata is believed to be an autoimmune disease resulting from a breach in the immune privilege of the hair follicles causing non scarring hair loss. Methods: our study included 40 patients from may 2019 to july 2022 diagnosed clinically, dermatoscopically and pathologically as alopecia areata Data were enrolled from department of dermatology and venereology, Al-Hussein hospital.

Completed3 enrollment criteria

Topical Cetirizine in Treatment of Localized Alopecia Areata

Alopecia Areata

Evaluate and compare the efficacy and safety of topical cetirizine 1%, versus topical betamethasone valerate 0.1% in the treatment of localized alopecia areata.

Not yet recruiting14 enrollment criteria

Effectiveness of Combination Therapy of Microneedling and Minoxidil in Androgenetic Alopecia of...

Androgenetic Alopecia

The goal of this clinical trial is to compare the effectiveness of combination therapy of microneedling and minoxidil in androgenetic alopecia of Indonesian men. The main questions it aims to answer are: Is there an increase in hair density with combination therapy of microneedling and minoxidil versus minoxidil monotherapy? Is there an increase in hair diameter with combination therapy of microneedling and minoxidil versus minoxidil monotherapy? Participants will be divided into 2 groups. The first one will receive minoxidil monotherapy, and the second one will receive a combination therapy of microneedling and minoxidil. Researchers will compare those 2 groups to see if there is a difference of effectiveness based on hair density and diameter.

Completed10 enrollment criteria

Study to Investigate the Effectiveness of a Topical Cosmetic Formulation DA-OTC-002

Hair DiseasesAlopecia1 more

The primary objective of the study was to assess the efficacy of DA-OTC-002 as a topical cosmetic hair treatment. The investigators conducted a prospective, institution-level, interventional, single-blinded, placebo-controlled investigation to assess the efficacy of a combination an alpha-1 agonist and a TAAR receptor agonist (DA-OTC-002) as a topical cosmetic hair treatment.

Completed15 enrollment criteria

Nutraceutical Supplement With Vegan Botanicals in Females With Self-Perceived Thinning Hair

Hair Thinning

The purpose of the study is to evaluate the safety and efficacy of a vegan nutraceutical supplement with standardized botanicals in females leading a more plant-based lifestyle with self-perceived thinning hair

Completed29 enrollment criteria

Study To Evaluate The Efficacy And Safety Profile Of PF-06651600 And PF-06700841 In Subjects With...

Alopecia Areata

This is a Phase 2a, randomized, double blind, parallel group, multicenter study with an extension period. The study will have a maximum duration of approximately 113 weeks. This includes an up to 5 weeks Screening Period, a 24 week Treatment Period, a 4 week Drug Holiday (#1), an up to 12 month Single Blind (investigator open, sponsor open and subject blind) Extension Period, a 4 week drug holiday (#2), a 6 month Cross Over Open Label Extension Period and a 4 week Follow up Period.

Completed9 enrollment criteria
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