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A Phase I, Single-dose Study with SB206 in Healthy Japanese Adults

A Phase I, Single-dose Study with SB206 in Healthy Japanese Adults

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2031220073
Enrollment
20
Registered
2022-05-19
Start date
2022-06-23
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Molluscum contagiosum

Interventions

SB206 and vehicle are applied.

Sponsors

Tsubouchi Ichiro
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Healthy Japanese adult males aged 20 to 40 years at the time of obtaining written informed consent 2. Subjects with a body mass index (BMI) of 18.5 to 25.0 at screening 3. Subjects who are considered by the investigator or subinvestigator as acceptable for inclusion in the study as judged from the results of observation and examination upon screening and hospitalization 4. Subjects who received full explanations regarding the objective of the study, details of the study and the study drug and provided voluntary written informed consent

Exclusion criteria

Exclusion criteria: 1. Subjects with a history of drug allergy 2. Subjects with a history of food allergy 3. Subjects with a history of contact dermatitis, such as adhesive tape dermatitis, or mechanical urticaria 4. Subjects considered ineligible for the study by the investigator or subinvestigator

Design outcomes

Primary

MeasureTime frame
Skin irritation

Contacts

Public ContactClinical Trials Information Desk

Sato Pharmaceutical Co., Ltd.

clinicaltrials-info@sato-seiyaku.co.jp+81-3-5412-7329

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026