Efficacy and Safety of ACH24 in the Treatment of Vitiligo

Ache Laboratorios Farmaceuticos

Status and phase

Withdrawn

Phase 3

Conditions

Vitiligo

Treatments

Drug: Group 01

Drug: Group 02

Study type

Interventional

Funder types

Industry

Identifiers

NCT01419964

ACH-VTL-03(09/11)

Details and patient eligibility

About

This is a multicenter clinical trial, phase III, randomized, placebo-controlled, parallel group, enroll 94 patients, to assess the efficacy of ACH24 in the repigmentation of achromatic areas in patients with vitiligo.

Full description

To evaluate the efficacy and safety of ACH24 compared to placebo in the treatment of vitiligo.The present study aims to register a new product in the country, the ACH24 for the treatment of vitiligo.

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients of both sexes, aged between 18 and 65 years, remaining the feasibility of a legal guardian in accordance with need, able to understand and provide written informed consent and able to allow compliance at the treatment and the requirements of the protocol;
Presence of generalized vitiligo;
Able to comprehend and willing to provide written informed consent in accordance with institutional and regulatory guidelines.

Exclusion criteria

Patients with:
- Inflammatory diseases;
- Alopecia Areata;
- Diabetes Type I;
- Asthma;
- Collagen disease;
- Atopic dermatitis;
- Psoriasis;
- Autoimmune thyroid disease (self reported). ¬ Thyroid problems (represents 15% of people with vitiligo), exclude only those who need to do treatment with corticosteroid or immunosuppressive.
Women of childbearing age who had tested positive for pregnancy, or who do not use acceptable contraceptive method, or do not agree to practice reliable contraception during the study;
Woman in pregnancy or lactation period;
Known allergic reaction against the phytomedicine as assessed by medical history;
Patient that is taking any prohibited medication (Item 9.3);
Participation in last one year of clinical protocols, unless it can be direct benefit to subject;
Any finding of clinical observation (anamnesis and physical exam) laboratory abnormality (eg, blood glucose, blood count), disease (for example, liver, cardiovascular system, lung) or therapy that, in opinion of the investigator, may endanger the subject or interfere with the endpoints of study.