Overview

Study to Investigate the Pharmacokinetics, Safety, and Tolerability of BMT101 in Healthy Male Volunteers

Status:
Completed
Trial end date:
2018-02-14
Target enrollment:
0
Participant gender:
Male
Summary
Phase I Study to Investigate the Pharmacokinetics, Safety, and Tolerability of BMT101 in Healthy Male Volunteers
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Hugel
Criteria
Inclusion Criteria:

1. Adults, 19 ~ 39 years of age

2. Body Mass Index (BMI) between 19 to 25kg/㎡ (19kg/㎡ ≤ BMI < 25kg/㎡) and weight at least
50kg on the day of screening

3. Medically healthy with no clinically significant findings on vital signs during the
screening period

4. Medically healthy with no clinically significant findings on physical examinations
during the screening period

Exclusion Criteria:

1. Subjects with clinically significant medical or surgical history described below
Clinically significant observations considered as unsuitable based on medical
judgement by investigators

- Skin disorder (psoriasis or contact dermatitis) which may affect absorption of
the investigational product, or scar, skin abnormality, history of surgery
(excluding simple appendectomy or herniorrhaphy) which can interrupt intradermal
injections

2. History of clinically significant allergy, cardiovascular, peripheral vascular, skin,
mucocutaneous, ocular, respiratory, musculoskeletal or any other conditions which can
be problems for pharmacokinetic evaluation

3. Donated blood or blood components or had been transfused plasma within 60 days prior
to the day of screening

4. Tobacco use within 30 days prior to the day of screening