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A repeatedly applied study of BBI-4000 in patients with primary hyperhidrosis

A repeatedly applied study of BBI-4000 in patients with primary hyperhidrosis

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080224187
Enrollment
25
Registered
2018-12-13
Start date
2019-01-19
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

Primary axillary hyperhidrosis

Interventions

investigational material(s) Generic name etc : BBI-4000 INN of investigational material : sofpironium bromide Therapeutic category code : 129 Other agents affecting peripheral nervous system Dosage an

Sponsors

KAKEN PHARMACEUTICAL, CO., LTD.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients diagnosed as primary axillary hyperhidrosis

Exclusion criteria

Exclusion criteria: Secondary hyperhidrosis

Design outcomes

Primary

MeasureTime frame
pharmacokinetics Plasma BBI-4000 level

Secondary

MeasureTime frame
safety Adverse event

Countries

Japan

Outcome results

None listed

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