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A Double-Blind Study of SB206 in Japanese Patients with Molluscum Contagiosum

A Double-Blind Study of SB206 in Japanese Patients with Molluscum Contagiosum

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2031240677
Enrollment
500
Registered
2025-02-14
Start date
2025-03-07
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

Treatment Group: SB206 is applied once daily for 12 weeks. Control Group: Vehicle is applied once daily for 12 weeks.

Sponsors

Kaneko Yoshiyuki
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Japanese patients with molluscum contagiosum aged 2 years or older and in good general health; - Patients who are able to understand and follow study instructions or who have support from the parent or legal guardian; - Patients who have a documented informed consent from voluntary signed by subject or a representative (parent or legal guardian) who received full explanations regarding the objectives and details of the study and the study drug.

Exclusion criteria

Exclusion criteria: - Patients who have molluscum contagiosum only in periocular area; - Patients who have received any treatment for molluscum contagiosum during the 14 days prior to Baseline; - Patients who are suspected to be immunosuppressed or have immunodeficiency disorder, or are on immunosuppressive treatment; - Patients who have history or presence of clinically significant medical, psychiatric, or emotional condition that, in opinion of the investigator, would compromise the safety of the subject or the quality of the data.

Design outcomes

Primary

MeasureTime frame
Proportion of subjects with complete clearance of all treatable MC at Week 12.

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