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Double-Blind, Randomized, Placebo-Controlled, Phase 1b, Pharmacodynamic Trial of TEV-56192 Following a Single Intravenous Administration in Healthy Participants

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-507018-29-00
Acronym
TV56192-PD-10191
Enrollment
48
Registered
2024-02-22
Start date
2024-03-05
Completion date
2024-11-22
Last updated
2024-08-06

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

Conditions

Pruritus

Interventions

None listed

Sponsors

Teva Branded Pharmaceutical Products R&D Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

Denmark

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026